Frequently asked questions
Our team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.
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- http://localhost/pages/support/faqs/will-fusion-em-plex-em-sup-sup-assays-cover-igh-rearrangements
- http://localhost/pages/support/faqs/can-rapid-genes-be-ordered-in-my-own-vector
- http://localhost/pages/support/faqs/can-rapid-genes-be-ordered-in-tubes-is-there-a-minimum-number-required
- http://localhost/pages/support/faqs/what-storage-conditions-are-recommended-for-rapid-genes
- http://localhost/pages/support/faqs/if-my-rapid-gene-fails-to-meet-purity-and-yield-specifications-will-it-be-remade
- http://localhost/pages/support/faqs/what-plate-formats-are-rapid-genes-available-in
- http://localhost/pages/support/faqs/are-rapid-genes-ngs-verified
- http://localhost/pages/support/faqs/when-should-i-expect-my-rapid-gene(s)-to-ship
- http://localhost/pages/support/faqs/how-long-is-my-data-retained-in-the-rhampseq-crispr-analysis-tool
- http://localhost/pages/support/faqs/what-manufacturing-grade-of-guide-rna-products-does-idt-offer
- http://localhost/pages/support/faqs/what-is-the-difference-between-idt-s-ruo-crispr-products-and-those-made-under-cgmp-processes
- http://localhost/pages/support/faqs/what-chemical-modifications-are-available-for-pre-cgmp-(engineering-run)-and-cgmp-guide-rnas
- http://localhost/pages/support/faqs/what-are-the-scales-and-lengths-of-guide-rnas
- http://localhost/pages/support/faqs/what-is-the-typical-qc-and-analytical-testing-offered-for-the-pre-cgmp-(engineering-run)-and-cgmp-guide-rna-manufacturing-services
- http://localhost/pages/support/faqs/how-do-i-order-pre-cgmp-(engineering-run)-and-or-cgmp-guide-rna-manufacturing-services-from-idt
- http://localhost/pages/support/faqs/does-idt-offer-regulatory-services
- http://localhost/pages/support/faqs/i-am-struggling-to-achieve-the-3x-minimum-yield-with-the-xgen-cfdna-ffpe-dna-library-prep-v2-mc-kit-for-the-maximum-input-into-hybridization-capture-how-could-i-proceed-with-using-the-xgen-pre-hyb-normalase-module-96-rxn
- http://localhost/pages/support/faqs/what-kind-of-samples-should-i-use-with-xgen-pre-hyb-normalase-module-96-rxn
- http://localhost/pages/support/faqs/how-much-time-does-it-take-to-run-the-xgen-pre-hyb-normalization-protocol
- http://localhost/pages/support/faqs/how-many-dna-libraries-can-i-multiplex-with-xgen-pre-hyb-normalase-module-96-rxn
- http://localhost/pages/support/faqs/which-library-preparation-workflows-are-supported-for-the-xgen-pre-hyb-normalase-module-96-rxn
- http://localhost/pages/support/faqs/which-insert-sizes-are-appropriate-to-use-with-the-xgen-pre-hyb-normalase-module-96-rxn
- http://localhost/pages/support/faqs/why-do-i-need-a-3x-normalization-minimum
- http://localhost/pages/support/faqs/when-should-i-use-the-xgen-pre-hyb-normalase-module-96-rxn
- http://localhost/pages/support/faqs/is-the-xgen-pre-hyb-normalase-module-96-rxn-different-from-the-xgen-normalase-module
- http://localhost/pages/support/faqs/what-does-the-xgen-pre-hyb-normalase-module-96-rxn-do
- http://localhost/pages/support/faqs/will-idt-store-my-vector
- http://localhost/pages/support/faqs/what-if-my-vector-does-not-meet-the-requirements-above
- http://localhost/pages/support/faqs/are-the-custom-genes-delivered-as-linear-fragments-or-in-a-vector
- http://localhost/pages/support/faqs/what-is-required-for-the-insertion-site
- http://localhost/pages/support/faqs/what-type-of-plasmid-prep-is-required-for-my-custom-vector
- http://localhost/pages/support/faqs/what-are-the-requirements-for-my-custom-vector
- http://localhost/pages/support/faqs/can-i-analyze-dna-and-rna-simultaneously-for-comprehensive-genomic-profiling-of-blood-cancers-with-archer-panels
- http://localhost/pages/support/faqs/what-does-it-mean-for-primers-to-be-functionally-tested
- http://localhost/pages/support/faqs/why-do-fusion-em-plex-em-assays-use-rna-instead-of-dna-as-input-material
- http://localhost/pages/support/faqs/is-it-possible-to-detect-low-allele-frequency-(-1-af)-variants-with-variant-em-plex-em-panels
- http://localhost/pages/support/faqs/can-i-analyze-solid-tumor-dna-and-rna-simultaneously-for-comprehensive-genomic-profiling-with-archer-panels
- http://localhost/pages/support/faqs/can-variant-em-plex-em-assays-be-used-for-somatic-and-germline-evaluation
- http://localhost/pages/support/faqs/how-do-labs-access-archer-analysis-software
- http://localhost/pages/support/faqs/what-is-the-difference-between-anchored-multiplex-pcr-(amp-)-and-traditional-priming-methods-for-dna-ngs-analysis
- http://localhost/pages/support/faqs/is-snv-indel-calling-supported-in-(rna-based)-fusion-em-plex-em-panels
- http://localhost/pages/support/faqs/does-archer-analysis-meet-compliance-standards-for-data-privacy-and-security
- http://localhost/pages/support/faqs/can-immuno-em-verse-em-provide-relevant-information-for-solid-tumors
- http://localhost/pages/support/faqs/can-immuno-em-verse-em-assays-detect-somatic-hypermutation-in-chronic-lymphocytic-leukemia
- http://localhost/pages/support/faqs/what-is-the-difference-between-anchored-multiplex-pcr-(amp-)-and-opposing-primer-methods-for-rna-ngs-analysis
- http://localhost/pages/support/faqs/how-much-does-archer-analysis-unlimited-cost
- http://localhost/pages/support/faqs/why-is-detecting-known-and-novel-fusions-important
- http://localhost/pages/support/faqs/how-is-liquidplex-optimized-to-amplify-cell-free-dna-(cfdna)-from-plasma-samples
- http://localhost/pages/support/faqs/how-would-choosing-one-of-these-nucleases-help-my-program-progress-to-the-clinic
- http://localhost/pages/support/faqs/are-the-ruo-and-gmp-products-the-same
- http://localhost/pages/support/faqs/where-are-the-products-manufactured
- http://localhost/pages/support/faqs/what-is-the-shelf-life-of-the-product
- http://localhost/pages/support/faqs/what-are-the-key-differences-between-spyfi-and-eureca-v
- http://localhost/pages/support/faqs/what-is-the-lead-time-for-gmp-product
- http://localhost/pages/support/faqs/can-aldevron-provide-necessary-manufacturing-information-to-support-regulatory-filings
- http://localhost/pages/support/faqs/can-aldevron-provide-regulatory-expertise-to-support-filings
- http://localhost/pages/support/faqs/can-you-share-details-on-the-analytical-methods-used-to-release-the-product
- http://localhost/pages/support/faqs/what-methods-are-recommended-to-quantify-my-libraries-prepared-using-xgen-pcr-free-adapters-for-ultima
- http://localhost/pages/support/faqs/can-i-use-the-xgen-stubby-adapter-(cat-10005974-10005924)-in-place-of-the-xgen-stubby-adapter-for-dnbseq
- http://localhost/pages/support/faqs/what-is-the-difference-between-xgen-library-amp-primer-mix-for-dnbseq-and-other-library-amplification-mixes-such-as-xgen-library-amplification-primer-mix
- http://localhost/pages/support/faqs/can-universal-or-standard-blocking-oligos-be-used-with-libraries-made-from-the-xgen-stubby-adapter-udi-primers-for-dnbseq
- http://localhost/pages/support/faqs/how-will-my-xgen-stubby-adapter-udi-primers-for-dnbseq-be-delivered
- http://localhost/pages/support/faqs/what-are-the-sequences-for-the-xgen-stubby-adapter-udi-primers-dnbseq
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-library-amp-primer-mix-dnbseq
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-universal-blockers-for-dnbseq
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-stubby-adapter-udi-primers-for-dnbseq
- http://localhost/pages/support/faqs/can-indexing-pcr-be-carried-out-in-the-provided-96-well-plate-of-xgen-udi-primers-dnbseq
- http://localhost/pages/support/faqs/which-sequencing-platform-should-be-used-for-the-xgen-stubby-adapter-udi-primers-for-dnbseq
- http://localhost/pages/support/faqs/what-amount-of-xgen-stubby-adapter-udi-primers-for-dnbseq-should-i-use-for-library-prep
- http://localhost/pages/support/faqs/what-buffer-should-i-use-to-dilute-the-xgen-stubby-adapter-for-dnbseq
- http://localhost/pages/support/faqs/are-either-the-xgen-stubby-adapters-or-udi-primers-for-dnbseq-methylated
- http://localhost/pages/support/faqs/do-the-xgen-stubby-adapter-udi-primers-for-dnbseq-contain-umis
- http://localhost/pages/support/faqs/can-i-use-the-xgen-stubby-adapter-(catalog-10005974-10005924)-in-place-of-the-xgen-stubby-adapter-for-element
- http://localhost/pages/support/faqs/what-is-the-difference-between-xgen-library-amp-primer-mix-for-element-and-other-library-amplification-mixes-such-as-xgen-library-amplification-primer-mix
- http://localhost/pages/support/faqs/can-universal-or-standard-blocking-oligos-be-used-with-libraries-made-from-xgen-stubby-adapter-udi-primers-for-element
- http://localhost/pages/support/faqs/how-will-my-xgen-stubby-adapter-udi-primers-for-element-be-delivered
- http://localhost/pages/support/faqs/what-plate-sealing-guidelines-should-i-follow-when-fewer-than-16-or-96-libraries-are-prepared
- http://localhost/pages/support/faqs/what-are-the-sequences-for-the-xgen-stubby-adapter-udi-primers-for-element
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-library-amp-primer-mix-for-element
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-universal-blockers-for-element
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-stubby-adapter-udi-primers-for-element
- http://localhost/pages/support/faqs/which-sequencing-platform-should-be-used-for-the-xgen-stubby-adapter-udi-primers-for-element
- http://localhost/pages/support/faqs/what-amount-of-xgen-stubby-adapter-udi-primers-for-element-should-i-use-for-library-prep
- http://localhost/pages/support/faqs/what-buffer-should-i-use-to-dilute-the-xgen-stubby-adapter-for-element
- http://localhost/pages/support/faqs/are-either-the-xgen-stubby-adapter-or-udi-primers-for-element-methylated
- http://localhost/pages/support/faqs/do-the-xgen-trade-stubby-adapter-udi-primers-for-element-contain-umis
- http://localhost/pages/support/faqs/my-crispr-genome-editing-efficiency-seems-very-low.-are-there-any-steps-i-can-take-to-improve-this
- http://localhost/pages/support/faqs/do-any-of-the-xgen-adapters-or-indexing-primers-for-ultima-contain-umis
- http://localhost/pages/support/faqs/are-any-of-the-xgen-adapters-or-indexing-primers-for-ultima-methylated
- http://localhost/pages/support/faqs/what-buffer-should-i-use-to-dilute-the-xgen-stubby-adapter-xgen-pcr-free-adapters-for-ultima-and-xgen-hybcap-adapters-for-ultima
- http://localhost/pages/support/faqs/how-will-my-xgen-pcr-free-adapters-for-ultima-or-xgen-hybcap-adapters-for-ultima-be-delivered
- http://localhost/pages/support/faqs/how-will-my-xgen-indexing-primers-for-ultima-be-delivered
- http://localhost/pages/support/faqs/can-universal-or-standard-blocking-oligos-be-used-with-libraries-made-from-the-xgen-adapters-and-indexing-primers-for-ultima
- http://localhost/pages/support/faqs/what-amount-of-xgen-adapters-or-indexing-primers-for-ultima-should-i-use-for-library-prep
- http://localhost/pages/support/faqs/which-sequencing-platform-should-be-used-for-the-xgen-adapters-or-indexing-primers-for-ultima
- http://localhost/pages/support/faqs/can-adapter-ligation-be-carried-out-in-the-provided-96-well-plate-of-xgen-pcr-free-adapters-for-ultima-or-xgen-hybcap-adapters-for-ultima
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-adapters-or-indexing-primers-for-ultima
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-universal-blockers-for-ultima
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-hybcap-library-amp-primer-mix-for-ultima
- http://localhost/pages/support/faqs/what-are-the-sequences-for-the-xgen-adapters-and-indexing-primers-for-ultima
- http://localhost/pages/support/faqs/what-is-the-difference-between-xgen-hybcap-lib-amp-primer-mix-for-ultima-and-other-library-amplification-mixes-such-as-xgen-library-amplification-primer-mix
- http://localhost/pages/support/faqs/what-are-the-dna-input-requirements-for-the-xgen-dna-library-prep-kits
- http://localhost/pages/support/faqs/can-the-xgen-ssdna-low-input-library-prep-kit-be-used-with-ancient-dna
- http://localhost/pages/support/faqs/what-sample-types-are-compatible-with-xgen-custom-amplicon-panels
- http://localhost/pages/support/faqs/how-long-can-i-leave-my-qpcr-mix-(containing-primetime-one-step-4x-broad-range-qpcr-master-mix)-at-room-temperature-(or-4-c)-and-still-generate-consistent-results
- http://localhost/pages/support/faqs/how-many-freeze-thaw-events-can-primetime-one-step-4x-broad-range-qpcr-master-mix-withstand
- http://localhost/pages/support/faqs/which-reference-dye-included-with-the-primetime-gene-expression-master-mix-the-primetime-one-step-rt-qpcr-master-mix-and-the-primetime-one-step-4x-broad-range-qpcr-master-mix
- http://localhost/pages/support/faqs/what-is-the-main-difference-between-the-primetime-one-step-rt-qpcr-master-mix-and-the-primetime-one-step-4x-broad-range-qpcr-master-mix
- http://localhost/pages/support/faqs/which-crude-non-extracted-sample-types-have-been-tested-with-the-primetime-one-step-4x-broad-range-qpcr-master-mix
- http://localhost/pages/support/faqs/when-should-the-direct-amplification-enhancer-included-with-the-primetime-one-step-4x-broad-range-qpcr-master-mix-be-used
- http://localhost/pages/support/faqs/can-i-store-primetime-one-step-4x-broad-range-qpcr-master-mix-at-room-temperature
- http://localhost/pages/support/faqs/my-primetime-one-step-4x-broad-range-qpcr-master-mix-got-stuck-in-shipping.-can-i-still-use-it
- http://localhost/pages/support/faqs/how-does-the-primetime-one-step-4x-broad-range-qpcr-master-mix-compare-with-one-step-master-mixes-from-other-manufacturers
- http://localhost/pages/support/faqs/which-cycling-parameters-will-give-me-the-best-results-when-using-the-primetime-one-step-4x-broad-range-qpcr-master-mix
- http://localhost/pages/support/faqs/how-many-freeze-thaw-events-can-the-primetime-one-step-rt-qpcr-master-mix-withstand
- http://localhost/pages/support/faqs/how-long-can-i-leave-qpcr-mix-(containing-primetime-one-step-rt-qpcr-master-mix)-at-4-c-and-still-generate-consistent-results
- http://localhost/pages/support/faqs/how-long-can-i-leave-qpcr-mix-(containing-primetime-one-step-rt-qpcr-master-mix)-at-room-temperature-and-still-generate-consistent-results
- http://localhost/pages/support/faqs/my-primetime-one-step-rt-qpcr-master-mix-got-stuck-in-shipping-can-i-still-use-it
- http://localhost/pages/support/faqs/what-cycling-parameters-will-give-me-the-best-results-when-using-primetime-one-step-rt-qpcr-master-mix
- http://localhost/pages/support/faqs/what-types-of-modifications-are-routinely-used-in-antisense-experiments-
- http://localhost/pages/support/faqs/how-does-the-primetime-one-step-rt-qpcr-master-mix-compare-with-one-step-master-mixes-from-other-manufacturers
- http://localhost/pages/support/faqs/can-i-store-primetime-one-step-rt-qpcr-master-mix-at-room-temperature
- http://localhost/pages/support/faqs/does-idt-offer-aso-designs-services
- http://localhost/pages/support/faqs/do-asos-need-to-be-hplc-purified
- http://localhost/pages/support/faqs/how-can-i-assess-knockdown-of-my-target-gene
- http://localhost/pages/support/faqs/how-much-aso-should-i-use-in-my-knockdown-experiment
- http://localhost/pages/support/faqs/what-is-the-purpose-of-asos-modified-in-a-gapmer-format
- http://localhost/pages/support/faqs/what-is-the-difference-between-2-ome-and-affinity-plus-modified-asos
- http://localhost/pages/support/faqs/does-idt-offer-crispr-screening-analysis-solutions
- http://localhost/pages/support/faqs/does-idt-offer-crispr-library-design-services
- http://localhost/pages/support/faqs/i-want-to-target-each-of-my-genes-with-multiple-guides.-how-many-grnas-do-you-suggest-per-gene
- http://localhost/pages/support/faqs/what-synthetic-arrayed-library-formats-are-available-from-idt-are-additional-customization-options-possible
- http://localhost/pages/support/faqs/what-are-the-advantages-of-an-arrayed-crispr-screen-over-a-pooled-screen
- http://localhost/pages/support/faqs/what-is-the-difference-between-arrayed-and-pooled-crispr-grna-libraries
- http://localhost/pages/support/faqs/what-type-of-crispr-guide-rna-libraries-does-idt-offer
- http://localhost/pages/support/faqs/what-are-the-new-names-of-idt-next-generation-sequencing-products
- http://localhost/pages/support/faqs/where-are-the-new-names-of-the-swift-products
- http://localhost/pages/support/faqs/what-is-the-new-name-of-the-xgen-lotus-dna-library-prep-kit
- http://localhost/pages/support/faqs/what-is-the-new-name-of-the-xgen-prism-dna-library-prep-kit
- http://localhost/pages/support/faqs/is-titration-of-adapters-required-for-different-input-amounts-for-the-xgen-dna-library-prep-kits
- http://localhost/pages/support/faqs/how-many-cycles-of-library-amplification-should-be-used-for-the-xgen-dna-library-prep-kits
- http://localhost/pages/support/faqs/are-there-any-safe-stopping-points-throughout-the-xgen-dna-library-prep-mc-workflow
- http://localhost/pages/support/faqs/why-are-xgen-udi-plate-2-8nt-and-the-xgen-cdi-primers-a-different-concentration-than-the-other-xgen-indexing-primers
- http://localhost/pages/support/faqs/where-can-i-find-the-index-sequences
- http://localhost/pages/support/faqs/what-sequencing-platform-should-be-used-for-the-xgen-stubby-adapter-and-unique-dual-index-primer-pairs
- http://localhost/pages/support/faqs/what-is-the-shelf-life-of-the-xgen-normalase-module
- http://localhost/pages/support/faqs/what-is-the-library-yield-requirement-for-expected-functionality-with-normalase-module
- http://localhost/pages/support/faqs/what-is-normalase-module
- http://localhost/pages/support/faqs/what-insert-sizes-are-appropriate-to-use-with-the-normalase-protocol
- http://localhost/pages/support/faqs/what-adapters-can-i-use-with-this-kit
- http://localhost/pages/support/faqs/what-size-fragments-can-be-converted-into-library-molecules
- http://localhost/pages/support/faqs/does-the-xgen-rna-library-prep-kit-include-upstream-poly(a)-enrichment-or-ribodepletion-modules
- http://localhost/pages/support/faqs/does-xgen-broad-range-rna-library-prep-kit-include-upstream-poly(a)-enrichment-or-ribodepletion-modules
- http://localhost/pages/support/faqs/what-methods-are-supported-for-dna-fragmentation-prior-to-library-construction
- http://localhost/pages/support/faqs/what-is-the-workflow-for-xgen-dna-library-prep-mc-dna-library-construction
- http://localhost/pages/support/faqs/what-is-the-shelf-life-and-recommended-storage-conditions-for-xgen-dna-library-preparation-kits
- http://localhost/pages/support/faqs/what-can-cause-under-fragmentation-of-dna
- http://localhost/pages/support/faqs/what-can-cause-over-fragmentation-of-dna-samples
- http://localhost/pages/support/faqs/what-are-the-major-steps-in-the-xgen-dna-library-prep-ez-kit-library-construction
- http://localhost/pages/support/faqs/what-are-the-input-ranges-for-working-with-the-xgen-dna-library-prep-mc-kit-or-the-xgen-dna-library-prep-ez-kit
- http://localhost/pages/support/faqs/what-hifi-polymerases-are-compatible-with-normalase-pcr
- http://localhost/pages/support/faqs/what-causes-variation-of-read-counts-(cv-10-)-among-libraries-within-normalase-pools
- http://localhost/pages/support/faqs/what-are-the-supported-library-preparation-workflows-for-xgen-normalase-module
- http://localhost/pages/support/faqs/is-there-a-minimum-or-maximum-limit-to-the-number-of-samples-that-can-be-placed-into-a-single-normalase-pool
- http://localhost/pages/support/faqs/is-library-amplification-required-when-using-the-normalase-module
- http://localhost/pages/support/faqs/does-this-normalase-protocol-support-library-long-term-storage
- http://localhost/pages/support/faqs/does-the-normalase-module-replace-post-pcr-library-quantification
- http://localhost/pages/support/faqs/do-i-need-library-quantification-after-amplification-and-before-normalase-i-enzyme
- http://localhost/pages/support/faqs/can-i-use-the-xgen-udi-plate-1-8-nt-and-xgen-udi-plate-2-8-nt-together
- http://localhost/pages/support/faqs/can-i-analyze-normalase-pools-using-fluorometric-methods-such-as-bioanalyzer-or-qubit
- http://localhost/pages/support/faqs/are-there-specific-recommendations-for-alternative-pooling-strategies
- http://localhost/pages/support/faqs/are-there-any-safe-stopping-points-in-the-normalase-protocol
- http://localhost/pages/support/faqs/why-is-my-methylation-sequencing-run-exhibiting-low-q-scores
- http://localhost/pages/support/faqs/why-do-my-xgen-amplicon-libraries-have-low-yields-and-contain-primer-dimers
- http://localhost/pages/support/faqs/which-bisulfite-conversion-kits-are-compatible-with-the-xgen-methylation-sequencing-dna-library-prep-kit
- http://localhost/pages/support/faqs/what-indexing-primers-can-i-use-with-this-xgen-broad-range-rna-library-kit
- http://localhost/pages/support/faqs/what-indexing-primers-can-i-use-with-this-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/what-are-the-main-steps-for-library-construction-using-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/what-are-the-main-steps-for-library-construction-using-the-xgen-broad-range-library-prep-kit
- http://localhost/pages/support/faqs/what-are-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/what-are-the-input-requirements-for-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/how-does-the-16s-snapp-data-analysis-pipeline-work
- http://localhost/pages/support/faqs/what-are-the-input-requirements-for-xgen-broad-range-rna-library-prep-kit
- http://localhost/pages/support/faqs/how-do-i-quantify-and-characterize-xgen-broad-range-rna-libraries
- http://localhost/pages/support/faqs/since-the-xgen-amplicon-16s-panel-covers-all-9-variable-regions-of-the-16s-rrna-gene-should-we-expect-full-length-16s-gene-sequences-to-be-readily-assembled-from-sequencing-reads-derived-from-this-kit
- http://localhost/pages/support/faqs/how-do-i-quantify-and-characterize-xgen-rna-libraries
- http://localhost/pages/support/faqs/how-do-i-pair-the-output-of-my-poly(a)-enrichment-or-ribodepletion-kit-with-the-input-of-the-xgen-broad-range-rna-library-prep-kit
- http://localhost/pages/support/faqs/is-titration-of-adapters-required-for-lower-inputs-with-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/how-do-i-pair-the-output-of-my-poly(a)-enrichment-or-ribodepletion-kit-with-the-input-of-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/is-this-kit-compatible-with-my-own-indexing-primers-with-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/how-do-i-analyze-xgen-hs-egfr-pathway-amplicon-panel-data
- http://localhost/pages/support/faqs/is-there-a-recommended-bioinformatics-workflow-for-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/is-there-a-recommended-bioinformatics-workflow-for-the-xgen-broad-range-library-prep-kit
- http://localhost/pages/support/faqs/is-the-xgen-methyl-seq-kit-compatible-with-reduced-representation-bisulfite-sequencing-(rrbs)
- http://localhost/pages/support/faqs/is-library-amplification-required-for-xgen-rna-library-prep-how-many-cycles-of-pcr-is-needed
- http://localhost/pages/support/faqs/does-the-xgen-broad-range-rna-library-prep-kit-work-with-damaged-or-degraded-rna
- http://localhost/pages/support/faqs/does-the-adaptase-tail-need-to-be-bioinformatically-trimmed-for-methylation-sequencing
- http://localhost/pages/support/faqs/does-the-xgen-amplicon-16s-snapp-pipeline-assemble-reads-to-full-length-16s-sequences
- http://localhost/pages/support/faqs/should-xgen-ssdna-low-input-dna-library-prep-kit-be-used-for-ffpe-samples
- http://localhost/pages/support/faqs/does-the-xgen-amplicon-16s-panel-enable-identification-of-bacteria-to-species-resolution
- http://localhost/pages/support/faqs/do-i-have-to-use-the-normalase-module-to-finish-my-xgen-amplicon-libraries
- http://localhost/pages/support/faqs/can-the-xgen-methylation-sequencing-dna-library-preparation-kit-be-used-with-ancient-dna
- http://localhost/pages/support/faqs/how-long-does-the-xgen-hs-egfr-pathway-amplicon-panel-protocol-take-to-complete
- http://localhost/pages/support/faqs/can-i-use-my-own-udi-indexing-primers-for-indexing-pcr-in-the-xgen-amplicon-sequencing-workflow
- http://localhost/pages/support/faqs/can-i-use-16s-and-its1-kits-together
- http://localhost/pages/support/faqs/can-i-order-my-own-custom-indexing-primers-(i.e.-udi)-with-appropriate-modifications-to-function-with-normalase-technology-in-the-xgen-amplicon-workflow
- http://localhost/pages/support/faqs/how-does-the-16s-snapp-pipeline-classify-sequences
- http://localhost/pages/support/faqs/can-i-generate-rna-libraries-of-different-size-ranges-with-the-xgen-rna-library-prep-kit
- http://localhost/pages/support/faqs/what-are-the-kit-shelf-life-and-recommended-storage-conditions
- http://localhost/pages/support/faqs/is-titration-of-adapters-required-for-lower-inputs
- http://localhost/pages/support/faqs/is-this-kit-compatible-with-my-own-indexing-primers
- http://localhost/pages/support/faqs/is-the-xgen-dna-library-prep-kit-mc-automation-friendly
- http://localhost/pages/support/faqs/how-does-the-16s-snapp-pipeline-estimate-the-abundance-of-different-organisms
- http://localhost/pages/support/faqs/is-library-amplification-required-how-many-cycles-of-pcr-is-needed
- http://localhost/pages/support/faqs/can-i-use-my-own-library-amplification-primers-or-indexing-amplification-primers-for-normalase-pcr
- http://localhost/pages/support/faqs/does-the-kit-work-with-damaged-or-degraded-rna
- http://localhost/pages/support/faqs/can-i-generate-rna-libraries-of-different-size-ranges
- http://localhost/pages/support/faqs/what-targets-are-covered-what-xgen-amplicon-hs-panels-are-available
- http://localhost/pages/support/faqs/are-there-truncated-products-in-a-standard-desalt-preparation-of-an-oligo
- http://localhost/pages/support/faqs/what-limit-of-detection-(lod)-is-achievable-with-for-xgen-hs-egfr-pathway-amplicon-panel
- http://localhost/pages/support/faqs/what-reverse-transcription-(rt)-module-is-recommended
- http://localhost/pages/support/faqs/what-sample-types-are-compatible-with-xgen-hs-egfr-pathway-amplicon-panel
- http://localhost/pages/support/faqs/how-do-i-perform-sars-cov-2-data-analysis
- http://localhost/pages/support/faqs/how-do-i-convert-qrt-pcr-ct-values-to-sars-cov-2-viral-copies
- http://localhost/pages/support/faqs/can-i-use-my-own-udi-primers-to-index-my-xgen-amplicon-libraries
- http://localhost/pages/support/faqs/how-much-dna-is-required-for-xgen-amplicon-hs-panels
- http://localhost/pages/support/faqs/can-bisulfite-conversion-replace-the-fragmentation-step-in-the-xgen-methyl-seq-library-prep-workflow
- http://localhost/pages/support/faqs/what-is-the-difference-between-alt-r-hdr-donor-blocks-and-megamer-single-stranded-dna-fragments
- http://localhost/pages/support/faqs/what-are-the-modifications-to-the-ends-of-alt-r-hdr-blocks-and-what-is-their-purpose
- http://localhost/pages/support/faqs/why-are-the-standard-ngs-reports-of-the-alt-r-hdr-donor-blocks-of-2000-base-pairs-or-shorter-titled-differently-than-those-longer-than-2000-base-pairs
- http://localhost/pages/support/faqs/why-does-idt-offer-an-additional-ngs-service-for-the-alt-r-hdr-blocks
- http://localhost/pages/support/faqs/i-have-a-question-related-to-pricing-on-my-order-account-who-should-i-contact-for-more-information
- http://localhost/pages/support/faqs/my-organization-is-tax-exempt.-where-do-i-find-documents-showing-our-tax-exempt-status-and-where-should-i-send-them
- http://localhost/pages/support/faqs/how-do-i-know-if-my-organization-has-submitted-tax-exemption-documents
- http://localhost/pages/support/faqs/my-organization-is-tax-exempt.-why-do-i-see-tax-on-my-order
- http://localhost/pages/support/faqs/what-information-can-i-find-in-the-order-status-tracker
- http://localhost/pages/support/faqs/where-do-i-find-the-order-status-tracker
- http://localhost/pages/support/faqs/what-is-the-order-status-tracker
- http://localhost/pages/support/faqs/does-idt-regularly-perform-in-silico-analysis-of-covid-variants
- http://localhost/pages/support/faqs/i-transfected-the-cells-with-alt-r-s.p.-cas9-gfp.-when-should-i-sort-the-cells-by-fluorescence-activated-cell-sorting-(facs)-to-enrich-for-transfected-cells
- http://localhost/pages/support/faqs/can-alt-r-s.p.-cas9-gfp-be-used-with-the-same-protocols-as-alt-r-s.p.-cas9-nuclease-v3
- http://localhost/pages/support/faqs/what-is-the-difference-between-a.s.-and-l.b.-cas12a-when-should-i-use-one-or-the-other
- http://localhost/pages/support/faqs/when-should-i-consider-using-the-glycerol-free-cas9-nuclease-instead-of-the-nucleases-that-include-glycerol
- http://localhost/pages/support/faqs/what-should-i-do-if-the-idt-online-ordering-tool-says-that-my-alt-r-hdr-donor-block-is-too-complex-to-order
- http://localhost/pages/support/faqs/is-the-alt-r-hdr-enhancer-v2-compatible-with-alt-r-hdr-donor-blocks
- http://localhost/pages/support/faqs/what-should-i-do-if-my-hdr-edit-did-not-work
- http://localhost/pages/support/faqs/do-i-need-to-include-the-electroporation-enhancer-in-my-electroporation-experiments-if-i-am-also-including-an-alt-r-hdr-donor-block
- http://localhost/pages/support/faqs/does-idt-offer-larger-sizes-of-alt-r-hdr-donor-blocks
- http://localhost/pages/support/faqs/what-are-optimum-storage-conditions-for-alt-r-hdr-donor-blocks
- http://localhost/pages/support/faqs/how-should-i-resuspend-the-alt-r-hdr-donor-block
- http://localhost/pages/support/faqs/does-idt-offer-labready-alt-r-hdr-donor-blocks
- http://localhost/pages/support/faqs/when-designing-donor-dna-for-use-in-hdr-what-are-the-optimal-lengths-of-the-left-and-right-homology-arms
- http://localhost/pages/support/faqs/what-is-the-optimal-amount-of-alt-r-hdr-donor-blocks-to-use-with-my-cell-type-and-what-can-i-do-to-prevent-toxicity-and-or-cell-death-after-delivering-alt-r-hdr-donor-blocks
- http://localhost/pages/support/faqs/do-the-universal-terminal-sequences-or-modifications-on-alt-r-hdr-donor-blocks-integrate-or-affect-insertion-rates
- http://localhost/pages/support/faqs/1.-how-are-the-alt-r-hdr-donor-blocks-modified-and-does-idt-offer-custom-modifications-for-alt-r-hdr-donor-blocks
- http://localhost/pages/support/faqs/i-found-a-mutation-in-my-clone.-is-there-a-problem-with-the-gblocks-gene-fragment
- http://localhost/pages/support/faqs/what-can-i-do-if-i-do-not-get-any-colonies-during-my-cloning-reaction-using-gBlocks-gene-fragments
- http://localhost/pages/support/faqs/what-should-i-do-if-the-idt-online-ordering-tool-says-that-my-sequence-is-too-complex-to-order-but-i-need-it-as-is
- http://localhost/pages/support/faqs/can-i-do-a-restriction-digest-directly-on-my-gblocks-gene-fragment-prep
- http://localhost/pages/support/faqs/how-can-I-use-PCR-to-add-overlapping-regions-to-my-gBlocks-Gene-Fragments-that-I-will-use-in-a-seamless-cloning-reaction
- http://localhost/pages/support/faqs/how-sensitive-is-the-rhampseq-crispr-analysis-system
- http://localhost/pages/support/faqs/why-is-it-that-my-main-rhampseq-custom-panel-or-rhampseq-crispr-panel-does-not-contain-assays-against-all-my-targets
- http://localhost/pages/support/faqs/what-type-of-analysis-can-be-performed-using-the-rhampseq-crispr-analysis-tool
- http://localhost/pages/support/faqs/how-do-i-design-a-rhampseq-crispr-panel-to-evaluate-on--and-off-target-editing-using-the-rhampseq-crispr-analysis-tool
- http://localhost/pages/support/faqs/how-do-i-identify-crispr-editing-off-target-sites
- http://localhost/pages/support/faqs/how-many-analysis-credits-are-used-for-each-rhampseq-crispr-analysis-tool-data-analysis-run
- http://localhost/pages/support/faqs/what-is-the-analysis-lab
- http://localhost/pages/support/faqs/what-is-the-analysis-platform-that-powers-the-rhampseq-crispr-analysis-tool
- http://localhost/pages/support/faqs/how-do-i-find-my-analysis-credit-balance
- http://localhost/pages/support/faqs/do-rhampseq-analysis-credits-expire
- http://localhost/pages/support/faqs/how-do-i-analyze-crispr-editing-next-generation-sequencing-(ngs)-data-with-the-rhampseq-crispr-analysis-tool
- http://localhost/pages/support/faqs/what-is-the-recommended-sequencing-depth-to-quantify-crispr-editing
- http://localhost/pages/support/faqs/what-crispr-enzymes-are-supported-by-the-rhampseq-crispr-analysis-tool
- http://localhost/pages/support/faqs/what-organisms-can-be-analyzed-using-the-rhampseq-crispr-analysis-tool
- http://localhost/pages/support/faqs/what-is-the-difference-between-the-rhampseq-crispr-library-kit-and-the-rhampseq-library-kit
- http://localhost/pages/support/faqs/what-crispr-nucleases-are-available-from-idt
- http://localhost/pages/support/faqs/what-purifications-are-supported-through-the-alt-r-crispr-custom-guide-rna-ordering-tool
- http://localhost/pages/support/faqs/should-pegrnas-for-crispr-prime-editing-include-chemical-modifications
- http://localhost/pages/support/faqs/how-can-users-include-modifications-or-base-types-other-than-what-is-available-in-the-alt-r-crispr-custom-guide-rna-ordering-tool
- http://localhost/pages/support/faqs/what-bases-and-chemical-modifications-are-supported-through-the-alt-r-crispr-custom-guide-rna-ordering-tool
- http://localhost/pages/support/faqs/how-do-i-resuspend-my-opools-oligo-pools-to-my-desired-concentration
- http://localhost/pages/support/faqs/how-long-can-i-leave-my-qpcr-mix-at-room-temperature-and-still-generate-consistent-results
- http://localhost/pages/support/faqs/why-does-the-reference-dye-come-in-a-tube-separate-from-the-primetime-gene-expression-master-mix
- http://localhost/pages/support/faqs/does-the-primetime-gene-expression-master-mix-use-a-hot-start-polymerase
- http://localhost/pages/support/faqs/is-the-primetime-gene-expression-master-mix-compatible-with-different-real-time-pcr-instruments-or-systems
- http://localhost/pages/support/faqs/how-much-reference-dye-should-i-add-to-the-primetime-sup-sup-gene-expression-master-mix
- http://localhost/pages/support/faqs/is-the-primetime-gene-expression-master-mix-appropriate-for-qpcr-assays-that-use-intercalating-dyes-(e.g.-sybr-green-and-evagreen-dyes)
- http://localhost/pages/support/faqs/can-the-primetime-gene-expression-master-mix-be-used-in-digital-pcr-experiments
- http://localhost/pages/support/faqs/does-the-primetime-gene-expression-master-mix-contain-ung
- http://localhost/pages/support/faqs/do-you-make-bhq-vic-probes-
- http://localhost/pages/support/faqs/what-is-crispr-and-how-does-it-work
- http://localhost/pages/support/faqs/what-are-optimum-storage-conditions-for-a-gblocks-hifi-gene-fragment
- http://localhost/pages/support/faqs/should-i-amplify-my-gblocks-hifi-gene-fragments-when-i-receive-them
- http://localhost/pages/support/faqs/how-do-i-design-my-gblocks-hifi-gene-fragment-for-restriction-cloning
- http://localhost/pages/support/faqs/can-i-get-gblocks-hifi-gene-fragments-outside-of-the-1000-3000-bp-range
- http://localhost/pages/support/faqs/how-is-a-gblocks-hifi-gene-fragment-different-from-a-gblocks-gene-fragment
- http://localhost/pages/support/faqs/how-much-xgen-udi-umi-adapters-should-i-use-for-library-prep
- http://localhost/pages/support/faqs/are-methylated-udi-umi-adapters-available
- http://localhost/pages/support/faqs/can-adapter-ligation-be-carried-out-in-the-provided-96-well-plate-of-xgen-udi-umi-adapters
- http://localhost/pages/support/faqs/can-the-xgen-unique-dual-index-umi-adapters-be-used-for-rna-seq
- http://localhost/pages/support/faqs/how-do-i-sequence-the-umi-in-the-xgen-udi-umi-adapters
- http://localhost/pages/support/faqs/do-i-need-to-titrate-the-adapters-when-using-different-input-amounts-with-the-xgen-cfDNA-and-FFPE-library-prep-kit
- http://localhost/pages/support/faqs/what-is-the-best-quantitation-method-for-assessing-the-quality-and-quantity-of-my-dna-before-preparing-libraries-with-the-xgen-cfdna-ffpe-library-prep-kit
- http://localhost/pages/support/faqs/what-adapters-should-i-use-with-the-xgen-cfdna-ffpe-dna-library-prep-kit
- http://localhost/pages/support/faqs/what-platform-should-be-used-for-sequencing-libraries-made-with-the-xgen-cfdna-ffpe-library-prep-kit
- http://localhost/pages/support/faqs/why-does-the-xgen-cfdna-ffpe-dna-library-prep-kit-have-fixed-instead-of-random-umis
- http://localhost/pages/support/faqs/what-are-the-best-applications-for-the-xgen-cfdna-ffpe-library-prep-kit
- http://localhost/pages/support/faqs/how-do-i-check-the-quality-of-sequencing-libraries-made-with-the-xgen-cfDNA-and-FFPE-library-prep-kit
- http://localhost/pages/support/faqs/are-there-stopping-points-in-the-xgen-prism-dna-library-prep-kit-protocol
- http://localhost/pages/support/faqs/do-i-need-to-shear-or-fragment-my-dna-before-using-the-xgen-cfDNA-and-FFPE-library-prep-kit
- http://localhost/pages/support/faqs/how-do-i-use-umis-for-error-correction
- http://localhost/pages/support/faqs/what-is-the-best-storage-condition-for-hdr-donor-oligos
- http://localhost/pages/support/faqs/when-using-the-hdr-design-tool-how-can-i-ensure-that-my-intended-changes-result-in-the-desired-coding-sequence-(such-as-insertion-of-a-stop-codon)
- http://localhost/pages/support/faqs/why-is-my-accession-number-not-found-by-the-hdr-design-tool
- http://localhost/pages/support/faqs/how-are-the-homology-arms-for-hdr-donor-oligos-selected-by-the-hdr-design-tool
- http://localhost/pages/support/faqs/i-already-have-my-hdr-donor-oligo-sequence.-can-i-use-the-hdr-design-tool-to-order-modified-hdr-oligos-containing-my-sequence
- http://localhost/pages/support/faqs/how-are-genomic-coordinates-defined
- http://localhost/pages/support/faqs/how-are-idt-hdr-donor-oligos-modified
- http://localhost/pages/support/faqs/how-do-i-incorporate-a-mutation-into-my-donor-template-using-the-hdr-design-tool
- http://localhost/pages/support/faqs/what-is-hdr
- http://localhost/pages/support/faqs/how-do-i-create-an-account
- http://localhost/pages/support/faqs/how-do-i-pay-invoices
- http://localhost/pages/support/faqs/how-can-i-download-my-invoice-specification-sheets-coa-or-qc-documents
- http://localhost/pages/support/faqs/how-do-i-save-items-to-my-wish-list
- http://localhost/pages/support/faqs/how-do-i-share-my-cart
- http://localhost/pages/support/faqs/how-do-i-request-a-quote
- http://localhost/pages/support/faqs/what-is-the-difference-between-the-locked-nucleic-acids-in-affinity-plus-qpcr-probes-and-primetime-lna-sup-sup-qpcr-probes
- http://localhost/pages/support/faqs/how-do-i-convert-my-yield-from-nanomoles-to-ods
- http://localhost/pages/support/faqs/what-is-the-turnaround-time-for-gene-synthesis-
- http://localhost/pages/support/faqs/what-is-the-length-of-synthetic-custom-genes-that-idt-can-synthesize-
- http://localhost/pages/support/faqs/can-i-order-eblocks-gene-fragments-in-a-plate-format-other-than-what-is-listed
- http://localhost/pages/support/faqs/do-you-recommend-using-eblocks-gene-fragments-to-assemble-larger-constructs
- http://localhost/pages/support/faqs/what-is-the-length-of-gblocks-gene-fragments-that-idt-can-synthesize
- http://localhost/pages/support/faqs/should-i-amplify-my-eblocks-gene-fragments-when-i-receive-them
- http://localhost/pages/support/faqs/what-restriction-sites-will-be-available-for-subcloning-with-my-gene-order-
- http://localhost/pages/support/faqs/should-i-amplify-my-gblocks-gene-fragments-when-i-receive-them-
- http://localhost/pages/support/faqs/how-long-does-it-take-to-make-a-gblocks-gene-fragment
- http://localhost/pages/support/faqs/can-idt-deliver-genes-in-custom-vectors-such-as-one-supplied-by-a-customer-
- http://localhost/pages/support/faqs/why-don-t-your-cloning-vectors-contain-multiple-cloning-sites-
- http://localhost/pages/support/faqs/what-is-the-difference-between-a-gblocks-gene-fragment-and-an-eblocks-gene-fragment
- http://localhost/pages/support/faqs/can-i-order-eblocks-gene-fragments-in-a-tube-format
- http://localhost/pages/support/faqs/how-do-i-design-my-eblocks-gene-fragment-for-restriction-cloning
- http://localhost/pages/support/faqs/what-are-optimum-storage-conditions-for-a-gblocks-gene-fragment
- http://localhost/pages/support/faqs/what-are-optimum-storage-conditions-for-a-custom-gene-
- http://localhost/pages/support/faqs/do-the-xgen-stubby-adapter-and-unique-dual-indexing-primers-contain-umis
- http://localhost/pages/support/faqs/what-are-the-shelf-life-and-recommended-storage-conditions-for-the-xgen-stubby-adapter-and-unique-dual-indexing-primers
- http://localhost/pages/support/faqs/how-much-xgen-stubby-adapter-and-unique-dual-indexing-primers-should-i-use-for-library-prep
- http://localhost/pages/support/faqs/what-buffer-should-be-used-to-dilute-the-xgen-stubby-adapter
- http://localhost/pages/support/faqs/are-the-xgen-stubby-adapter-and-unique-dual-indexing-primers-methylated
- http://localhost/pages/support/faqs/are-locked-nucleic-acids-available-for-custom-dna-and-rna-oligos
- http://localhost/pages/support/faqs/is-each-oligo-that-goes-into-opools-oligo-pools-manufactured-individually
- http://localhost/pages/support/faqs/are-there-any-desalting-or-purification-options-available-for-opools-oligo-pools
- http://localhost/pages/support/faqs/if-opools-oligo-pools-are-not-quantified-how-are-different-yield-options-offered
- http://localhost/pages/support/faqs/are-there-any-quality-guarantees-on-opools-oligo-pools-similar-to-other-idt-oligos
- http://localhost/pages/support/faqs/what-quality-control-is-done-on-opools-oligo-pools
- http://localhost/pages/support/faqs/what-diluent-options-are-available-for-opools-oligo-pools
- http://localhost/pages/support/faqs/how-do-i-order-pace-primers-and-pace-genotyping-master-mix
- http://localhost/pages/support/faqs/how-do-i-design-primers-for-pace-genotyping-assays
- http://localhost/pages/support/faqs/with-which-sequencing-protocols-are-xgen-hyb-panels-compatible
- http://localhost/pages/support/faqs/how-do-i-know-if-i-over-amplified-my-library
- http://localhost/pages/support/faqs/what-are-the-major-steps-in-library-construction-with-the-lotus-dna-library-prep-kit
- http://localhost/pages/support/faqs/how-many-cycles-of-library-amplification-should-be-used-with-the-lotus-dna-library-prep-kit
- http://localhost/pages/support/faqs/what-are-the-common-applications-for-the-xgen-dna-library-prep-kit-mc
- http://localhost/pages/support/faqs/custom-ngs-adapters-can-be-purchased-as-16-or-96-reactions-how-many-nanomoles-are-in-1-reaction
- http://localhost/pages/support/faqs/what-are-the-sequences-for-the-idt-and-illumina-indexes-idt-8-idt-10-ilmn-8-ilmn-10
- http://localhost/pages/support/faqs/can-1x-te-buffer-be-used-instead-of-idte-buffer-in-rhampseq-experiments
- http://localhost/pages/support/faqs/what-is-the-sequencing-performance-of-the-rhampseq-system
- http://localhost/pages/support/faqs/for-genotyping-applications-what-is-the-recommended-minimum-sequencing-coverage-per-assay
- http://localhost/pages/support/faqs/can-more-than-100-µl-of-rhampseq-library-pool-be-used-in-a-single-ampure-clean-up
- http://localhost/pages/support/faqs/how-is-the-concentration-of-each-primer-in-a-rhampseq-10x-forward-or-reverse-pool-calculated-for-a-500-plex-panel
- http://localhost/pages/support/faqs/what-sample-types-can-i-use-with-rhampseq-assays
- http://localhost/pages/support/faqs/what-are-the-advantages-of-the-rhampseq-library-preparation-protocol-and-the-rhampseq-high-throughput-library-preparation-protocol
- http://localhost/pages/support/faqs/why-does-the-rhamp-primer-in-my-rhampseq-assay-contain-an-n-base
- http://localhost/pages/support/faqs/how-much-time-does-each-rhampseq-protocol-require
- http://localhost/pages/support/faqs/why-did-some-of-my-targets-not-have-rhampseq-assay-designs
- http://localhost/pages/support/faqs/what-is-the-assay-call-accuracy-and-how-is-it-determined
- http://localhost/pages/support/faqs/why-is-the-term-reference-allele-used-vs.-wild-type-major-or-ancestral-allele-or-other-similar-terms
- http://localhost/pages/support/faqs/why-do-rhamp-snp-assays-have-higher-fluorescence-signal-compared-to-other-assay-types
- http://localhost/pages/support/faqs/what-platforms-have-been-tested-with-rhamp-snp-genotyping-assays
- http://localhost/pages/support/faqs/what-are-adme-genes
- http://localhost/pages/support/faqs/should-i-use-5-µl-or-10-µl-reaction-volumes-for-my-rhamp-snp-assays
- http://localhost/pages/support/faqs/does-the-rhamp-snp-assay-library-include-predesigned-assays-for-triallelic-snps-or-indels
- http://localhost/pages/support/faqs/do-i-need-to-use-blast-to-check-my-rhamp-snp-assay-primers-for-specificity
- http://localhost/pages/support/faqs/do-i-need-to-optimize-the-annealing-temperature-for-each-rhamp-snp-assay-i-order
- http://localhost/pages/support/faqs/how-should-i-determine-the-annealing-temperature-for-a-probe-based-qpcr-assay-should-i-select-a-tm-midway-between-my-primer-and-probe-tms-
- http://localhost/pages/support/faqs/when-designing-donor-dna-for-use-in-homology-directed-repair-(hdr)-what-are-the-optimal-lengths-of-the-left-and-right-homology-arms-and-what-is-the-maximum-size-of-sequence-that-can-be-efficiently-inserted-in-mammalian-cells
- http://localhost/pages/support/faqs/when-using-the-alt-r-sup-sup-s.p.-hifi-cas9-nuclease-3nls-do-i-follow-the-same-protocols-for-the-standard-alt-r-s.p.-cas9-nuclease-3nls
- http://localhost/pages/support/faqs/when-using-the-alt-r-sup-sup-cas9-nickases-do-i-follow-the-same-protocol-as-the-standard-alt-r-s.p.-cas9-nuclease-3nls
- http://localhost/pages/support/faqs/what-reagents-will-i-need-in-addition-to-the-alt-r-sup-sup-rnas-for-a-crispr-cpf1-genome-editing-experiment
- http://localhost/pages/support/faqs/what-methods-can-be-used-to-deliver-the-cpf1-ribonucleoprotein-(rnp)
- http://localhost/pages/support/faqs/what-makes-alt-r-sup-sup-s.p.-hifi-cas9-nuclease-3nls-a-high-fidelity-enzyme
- http://localhost/pages/support/faqs/what-is-the-recommended-length-for-the-crispr-cpf1-crrna-guide
- http://localhost/pages/support/faqs/what-is-the-protospacer-adjacent-motif-(pam)-sequence-for-cpf1-how-is-this-different-from-cas9
- http://localhost/pages/support/faqs/what-is-the-on-target-efficiency-of-the-alt-r-sup-sup-s.p.-hifi-cas9-nuclease-3nls
- http://localhost/pages/support/faqs/what-is-the-expected-reduction-in-off-target-effects-(otes)-when-using-alt-r-sup-sup-s.p.-hifi-cas9-nuclease-3nls
- http://localhost/pages/support/faqs/what-is-the-concentration-of-the-alt-r-sup-sup-cas9-nucleases-and-nickases
- http://localhost/pages/support/faqs/what-is-the-average-frequency-of-the-crispr-cas9-pam-sequence-in-the-mammalian-genome
- http://localhost/pages/support/faqs/what-is-alt-r-sup-sup-cpf1-electroporation-enhancer
- http://localhost/pages/support/faqs/what-is-alt-r-Cas12a-electroporation-enhancer
- http://localhost/pages/support/faqs/what-crispr-cpf1-crrna-controls-should-i-use
- http://localhost/pages/support/faqs/what-buffer-should-i-use-to-resuspend-the-cpf1-protein
- http://localhost/pages/support/faqs/what-buffer-should-i-use-to-resuspend-the-cas9-protein
- http://localhost/pages/support/faqs/should-i-use-the-alt-r-sup-sup-cas9-d10a-or-h840a-nickase
- http://localhost/pages/support/faqs/is-the-pam-sequence-part-of-the-crispr-cas9-crrna-construct
- http://localhost/pages/support/faqs/is-the-alt-r-sup-sup-crispr-cpf1-ribonucleoprotein-(rnp)-complex-stable-do-i-need-to-make-a-fresh-complex-for-each-experiment
- http://localhost/pages/support/faqs/is-the-alt-r-sup-sup-crispr-cas9-ribonucleoprotein-(rnp)-complex-stable-do-i-need-to-make-a-fresh-complex-for-each-experiment
- http://localhost/pages/support/faqs/is-it-possible-for-the-alt-r-sup-sup-cpf1-electroporation-enhancer-to-integrate-at-the-cpf1-cut-site
- http://localhost/pages/support/faqs/is-it-possible-for-the-alt-r-sup-sup-cas9-electroporation-enhancer-to-integrate-at-the-cas9-cut-site
- http://localhost/pages/support/faqs/if-the-target-area-does-not-contain-a-protospacer-adjacent-motif-(pam)-sequence-will-the-crispr-cas9-complex-bind
- http://localhost/pages/support/faqs/i-transfected-my-cells-with-the-fluorescently-labeled-alt-r-sup-sup-crispr-cas9-tracrrna-atto-550.-when-should-i-sort-my-cells-by-fluorescence-activated-cell-sorting-(facs)
- http://localhost/pages/support/faqs/i-cannot-see-crispr-cpf1-editing.-why
- http://localhost/pages/support/faqs/i-cannot-see-crispr-cas9-editing.-what-can-i-do
- http://localhost/pages/support/faqs/i-am-seeing-cell-death-after-crispr-rna-transfection-what-can-i-do-to-prevent-this
- http://localhost/pages/support/faqs/how-should-i-store-the-cpf1-protein
- http://localhost/pages/support/faqs/how-should-i-store-the-cas9-protein
- http://localhost/pages/support/faqs/how-should-i-deliver-the-crispr-cpf1-components-into-cells
- http://localhost/pages/support/faqs/how-much-fluorescently-labeled-tracrrna-should-i-use-in-my-crispr-cas9-experiments
- http://localhost/pages/support/faqs/how-much-alt-r-sup-sup-cpf1-electroporation-enhancer-should-i-use
- http://localhost/pages/support/faqs/how-much-alt-r-cas9-electroporation-enhancer-should-i-use-during-delivery-of-the-ribonucleoprotein-(rnp)-complex
- http://localhost/pages/support/faqs/how-many-experiments-can-i-expect-to-get-from-a-tube-of-cas9
- http://localhost/pages/support/faqs/how-far-apart-should-i-design-my-two-guides-when-using-the-alt-r-sub-sub-nickases
- http://localhost/pages/support/faqs/how-does-alt-r-sup-sup-s.p.-hifi-cas9-nuclease-3nls-differ-from-the-standard-alt-r-s.p.-cas9-nuclease-3nls
- http://localhost/pages/support/faqs/how-do-i-choose-which-two-guide-rnas-to-multiplex-when-using-the-alt-r-sup-sup-nickases
- http://localhost/pages/support/faqs/how-can-i-estimate-the-amount-of-editing-obtained-using-the-alt-r-sup-sup-crispr-cas9-or--cpf1-systems
- http://localhost/pages/support/faqs/how-can-i-ensure-i-am-designing-my-crispr-cpf1-crrna-guide-sequence-in-the-correct-orientation-and-to-the-appropriate-strand-what-sequence-should-be-input-into-the-crispr-cpf1-crrna-ordering-tool
- http://localhost/pages/support/faqs/do-you-offer-crispr-crrna-libraries
- http://localhost/pages/support/faqs/do-you-have-gmp-versions-of-the-alt-r-sup-sup-cas9-nucleases
- http://localhost/pages/support/faqs/do-i-need-to-form-my-grna-rnp-complexes-separately-before-multiplexing
- http://localhost/pages/support/faqs/can-the-alt-r-sup-sup-cpf1-electroporation-enhancer-negatively-impact-the-activity-of-my-guide
- http://localhost/pages/support/faqs/can-i-use-a-crispr-cas9-crrna-protospacer-sequence-that-is-shorter-than-20-nt
- http://localhost/pages/support/faqs/what-qpcr-products-does-idt-ship-at-ambient-temperature
- http://localhost/pages/support/faqs/where-can-i-review-all-the-supporting-data-for-shipping-primetime-gene-expression-master-mix-at-ambient-temperature
- http://localhost/pages/support/faqs/how-many-freeze-thaw-events-can-primetime-gene-expression-master-mix-withstand
- http://localhost/pages/support/faqs/can-i-store-primetime-gene-expression-master-mix-at-room-temperature
- http://localhost/pages/support/faqs/do-i-need-to-worry-about-performance-if-my-shipment-of-primetime-gene-expression-master-mix-is-delayed
- http://localhost/pages/support/faqs/do-i-need-to-reduce-thiol-modified-oligos-before-use-
- http://localhost/pages/support/faqs/will-polyacrylamide-gel-electrophoresis-damage-a-cy-labeled-oligonucleotide-
- http://localhost/pages/support/faqs/will-phosphothioate-(ps)-modifications-to-the-ends-of-pcr-primers-provide-nuclease-resistance-and-thus-a-longer-half-life-for-the-pcr-product-when-transfected-into-a-cell-
- http://localhost/pages/support/faqs/will-idt-synthesize-aptamers-for-me-
- http://localhost/pages/support/faqs/will-i-lose-more-oligo-when-resuspending-in-polystyrene-tubes-compared-with-polypropolyene-tubes-
- http://localhost/pages/support/faqs/why-should-i-sequence-multiple-colonies-when-cloning
- http://localhost/pages/support/faqs/why-should-i-consider-purification-of-my-oligos-
- http://localhost/pages/support/faqs/why-might-the-concentration-of-reference-dye-need-to-differ
- http://localhost/pages/support/faqs/why-is-the-tm-provided-on-your-oligonucleotide-specification-sheets-different-from-the-calculated-tm-i-obtained-when-i-designed-my-oligos-
- http://localhost/pages/support/faqs/why-is-purification-not-recommended-for-randomized-oligos-
- http://localhost/pages/support/faqs/why-is-page-purification-not-available-with-fluorescent-dyes-
- http://localhost/pages/support/faqs/why-does-the-tm-on-my-spec-sheet-differ-from-that-generated-by-the-idt-scitools-programs-(e.g.-realtime-pcr-oligoanalyzer-tools)-
- http://localhost/pages/support/faqs/why-does-the-shipped-quantity-of-product-vary-even-for-reorders-of-the-same-sequence-
- http://localhost/pages/support/faqs/why-does-the-read-depth-vary-across-the-sequence-data
- http://localhost/pages/support/faqs/why-does-my-sequence-data-have-errors
- http://localhost/pages/support/faqs/why-do-my-primers-have-deleted-3'-bases-in-the-amplified-fragment-when-i-use-a-proofreading-enzyme-for-pcr-
- http://localhost/pages/support/faqs/why-are-some-of-the-items-in-my-order-history-not-available-for-re-order-
- http://localhost/pages/support/faqs/why-are-my-oligos-a-yellow-brown-color
- http://localhost/pages/support/faqs/why-am-i-limited-to-18-n-or-k-mixed-bases-in-my-gblocks-gene-fragment-
- http://localhost/pages/support/faqs/which-repair-pathway-is-most-commonly-used-to-repair-crispr-mediated-double-stranded-breaks-nhej-or-hdr
- http://localhost/pages/support/faqs/which-negative-control-dicer-substrate-sirna-(dsirna)-should-i-choose-ds-nc1-or-ds-scrambledneg
- http://localhost/pages/support/faqs/which-is-the-best-way-to-deliver-oligos-into-cells-in-culture-
- http://localhost/pages/support/faqs/which-dyes-are-compatible-with-my-thermal-cycler-
- http://localhost/pages/support/faqs/which-dyes-are-available-for-use-with-the-idt-zen-quencher-
- http://localhost/pages/support/faqs/where-on-a-nucleotide-are-cy-dyes-attached-
- http://localhost/pages/support/faqs/where-is-the-notes-field-for-oligo-ordering
- http://localhost/pages/support/faqs/where-can-oligo-invoices-quality-control-documents-and-specification-sheets-be-found-online-
- http://localhost/pages/support/faqs/when-will-my-oligos-be-shipped-
- http://localhost/pages/support/faqs/when-using-the-idt-online-resuspension-calculator-(scitools)-is-it-more-accurate-to-use-extinction-coefficient-or-mw-for-single-stranded-oligos-
- http://localhost/pages/support/faqs/when-preparing-the-qpcr-reaction-mix-should-i-thaw-or-keep-reagents-(such-as-the-primetime-gene-expression-master-mix)-on-ice
- http://localhost/pages/support/faqs/when-designing-donor-dna-for-use-in-hdr-what-are-the-optimal-lengths-of-the-left-and-right-homology-arms-and-what-is-the-maximum-size-of-sequence-that-can-be-efficiently-inserted-in-mammalian-cells
- http://localhost/pages/support/faqs/when-calculating-the-tm-of-my-oligo-should-i-only-use-the-bases-which-are-complementary-to-my-target-or-should-i-also-include-any-sticky-overhangs-on-the-primer-
- http://localhost/pages/support/faqs/what-vectors-are-available-for-standard-gene-synthesis-orders-
- http://localhost/pages/support/faqs/what-types-of-sequence-motifs-should-be-avoided-when-ordering-gblocks-gene-fragments-
- http://localhost/pages/support/faqs/what-type-of-purification-should-i-choose-for-my-qpcr-primers-
- http://localhost/pages/support/faqs/what-tools-does-idt-provide-to-design-multiplex-qpcr-assays-
- http://localhost/pages/support/faqs/what-reagents-will-i-need-in-addition-to-the-alt-r-rnas-to-do-a-crispr-genome-editing-experiment
- http://localhost/pages/support/faqs/what-quality-checks-do-gblocks-gene-fragments-with-variable-bases-receive-
- http://localhost/pages/support/faqs/what-molar-concentrations-of-oligonucleotide-and-salts-are-used-to-calculate-the-tm-reported-on-specification-sheets-
- http://localhost/pages/support/faqs/what-modification-can-i-use-in-place-of-vic-
- http://localhost/pages/support/faqs/what-is-the-structure-of-the-zen-internal-quencher-
- http://localhost/pages/support/faqs/what-is-the-standard-desalting-procedure-idt-uses-for-newly-synthesized-oligos-and-what-additional-purification-options-do-i-have-
- http://localhost/pages/support/faqs/what-is-the-standard-delivery-vector-idt-uses-for-genes-and-mini-gene-synthetic-genes-
- http://localhost/pages/support/faqs/what-is-the-stability-of-rna-vs.-dna
- http://localhost/pages/support/faqs/what-is-the-stability-of-fluorescently-labeled-oligos-and-their-fluorescent-modifications
- http://localhost/pages/support/faqs/what-is-the-sodium-salt-exchange-for-that-is-done-post-hplc-purification-
- http://localhost/pages/support/faqs/what-is-the-shelf-life-of-my-oligo
- http://localhost/pages/support/faqs/what-is-the-optimal-length-of-a-primer-
- http://localhost/pages/support/faqs/what-is-the-length-of-the-teg-spacer-in-your-biotin-teg-modification-and-do-you-offer-a-longer-spacer-arm-than-teg-
- http://localhost/pages/support/faqs/what-is-the-fidelity-of-your-ultramer-oligonucleotide-synthesis-
- http://localhost/pages/support/faqs/what-is-the-difference-between-universal-and-standard-blocking-oligos-(used-in-ngs-experiments)-
- http://localhost/pages/support/faqs/what-is-the-difference-between-scale-and-yield-and-why-don-t-i-receive-that-full-amount-designated-by-the-scale-i-order-
- http://localhost/pages/support/faqs/what-is-the-difference-between-27-mer-sirnas-and-traditional-21-mer-sirnas-
- http://localhost/pages/support/faqs/what-is-the-design-or-catalog-id-for-my-dsirna
- http://localhost/pages/support/faqs/what-is-the-best-way-to-purify-pcr-products-
- http://localhost/pages/support/faqs/what-is-ce-service-
- http://localhost/pages/support/faqs/what-is-a-pam-sequence-and-where-is-it-located
- http://localhost/pages/support/faqs/what-if-i-need-a-gblocks-gene-fragment-library-that-is-more-complex-than-what-you-offer-online-
- http://localhost/pages/support/faqs/what-guarantees-are-associated-with-your-trifecta-kit-is-the-designed-rna-duplex-specific-
- http://localhost/pages/support/faqs/what-dyes-should-i-select-for-my-qpcr-assay-
- http://localhost/pages/support/faqs/what-dsirna-concentration-do-i-need-to-use-in-my-experiment-to-see-knockdown-
- http://localhost/pages/support/faqs/what-does-od-sub-260-sub-stand-for
- http://localhost/pages/support/faqs/what-does-idt-s-browser-warning-mean
- http://localhost/pages/support/faqs/what-cycling-parameters-will-give-me-the-best-results-when-using-the-primetime-gene-expression-master-mix
- http://localhost/pages/support/faqs/what-conditions-should-i-use-to-hplc-purify-my-oligos-
- http://localhost/pages/support/faqs/what-concentrations-are-the-primers-and-probe-in-the-primetime-qpcr-assay-
- http://localhost/pages/support/faqs/what-are-your-shipping-rates-
- http://localhost/pages/support/faqs/what-are-your-payment-terms-
- http://localhost/pages/support/faqs/what-are-the-restrictions-and-pricing-for-sameday-oligo-service-
- http://localhost/pages/support/faqs/what-are-the-n-and-k-mixed-bases-that-can-be-incorporated-into-the-variable-regions-of-gblocks-gene-fragments-
- http://localhost/pages/support/faqs/what-are-the-length-restrictions-for-your-dna-oligos-
- http://localhost/pages/support/faqs/what-are-the-differences-between-use-of-black-hole-quencher--1-vs-black-hole-quencher--2-dual-labeled-probes-
- http://localhost/pages/support/faqs/what-are-the-criteria-for-choosing-pcr-amplicon-length-
- http://localhost/pages/support/faqs/what-are-the-base-degeneracy-codes-that-you-use-(eg.-r-w-k-v-s)-
- http://localhost/pages/support/faqs/what-are-self--and-homo-dimers-and-how-do-i-select-primers-to-avoid-these-problems-
- http://localhost/pages/support/faqs/what-are-rna-oligo-chimeras
- http://localhost/pages/support/faqs/what-are-oligocard-payment-cards-
- http://localhost/pages/support/faqs/what-are-dna-rna-hybrid-oligos-used-for-and-can-idt-synthesize-them-
- http://localhost/pages/support/faqs/what-are-aptamers-and-why-are-they-growing-in-popularity-
- http://localhost/pages/support/faqs/what-are-amos-(mirna-inhibitors)-and-how-are-they-used-
- http://localhost/pages/support/faqs/there-are-no-pam-ngg-sequences-close-to-my-locus-of-interest.-what-can-i-do
- http://localhost/pages/support/faqs/should-rna-be-stored-differently-than-dna
- http://localhost/pages/support/faqs/should-i-order-my-gblocks-gene-fragment-with-the-5-phosphate-modification
- http://localhost/pages/support/faqs/should-i-only-be-concerned-about-sodium-ions-when-calculating-tm-
- http://localhost/pages/support/faqs/should-i-do-anything-to-prep-my-tube-of-oligo-before-resuspending-
- http://localhost/pages/support/faqs/should-i-avoid-purification-for-sequences-containing-mixed-bases-(degenerate-or-randomized-oligos)-
- http://localhost/pages/support/faqs/on-your-website-i-see-that-there-are-two-different-extinction-coefficients-for-various-dyes.-which-one-should-i-use
- http://localhost/pages/support/faqs/my-primers-are-not-amplifying-the-target-region-after-crispr-genome-editing.-what-could-cause-this
- http://localhost/pages/support/faqs/is-there-a-modification-you-would-recommend-to-block-the-3'-end-of-an-oligo-
- http://localhost/pages/support/faqs/is-the-pam-sequence-part-of-the-sgrna-sequence-construct
- http://localhost/pages/support/faqs/is-my-oligo-still-good-after-x-amount-of-time
- http://localhost/pages/support/faqs/is-mass-spectrometry-analysis-performed-on-oligonucleotides-before-they-are-shipped-
- http://localhost/pages/support/faqs/is-it-possible-to-synthesize-single-strand-dna-with-fluorescent-labeling-
- http://localhost/pages/support/faqs/is-it-possible-to-order-an-oligo-with-both-an-amino-modifier-modification-and-a-modification-attached-via-nhs-ester-chemistry-
- http://localhost/pages/support/faqs/is-it-possible-to-add-to-an-order-that-i-already-placed-
- http://localhost/pages/support/faqs/is-it-ok-to-resuspend-and-store-oligos-in-depc-treated-water-
- http://localhost/pages/support/faqs/is-idte-buffer-rnase-free-
- http://localhost/pages/support/faqs/is-a-pam-sequence-present-in-every-gene
- http://localhost/pages/support/faqs/in-what-direction-does-idt-synthesize-oligos-
- http://localhost/pages/support/faqs/in-calculating-tms-for-oligos-whose-nearest-neighbor-values-do-you-use
- http://localhost/pages/support/faqs/if-i-order-through-the-web-but-have-a-quote-for-better-pricing-how-do-i-specify-that-in-my-order-
- http://localhost/pages/support/faqs/i-ve-been-using-tsug-s-rule-to-calculate-the-tm-of-my-oligonucleotide.-is-that-still-the-best-method-to-calculate-tm
- http://localhost/pages/support/faqs/i-m-seeing-cell-death-after-crispr-rna-transfection.-what-can-i-do-to-prevent-this
- http://localhost/pages/support/faqs/i-received-my-shipment-and-it-is-marked-partial.-what-does-that-mean-
- http://localhost/pages/support/faqs/i-received-a-dry-oligo-and-the-tube-looks-empty.-should-i-be-able-to-see-the-oligo-
- http://localhost/pages/support/faqs/i-forgot-my-login-password.-how-can-i-retrieve-it-so-i-will-be-able-to-submit-my-orders-through-your-site-
- http://localhost/pages/support/faqs/i-am-trying-to-resuspend-my-oligo-but-i-still-see-some-film-at-the-bottom-of-the-tube.-does-the-film-contain-my-oligo-that-did-not-resuspend-into-solution-
- http://localhost/pages/support/faqs/i-am-performing-routine-pcr-cloning-and-amplicon-sequencing.-what-scale-should-i-use-for-oligo-synthesis-
- http://localhost/pages/support/faqs/i-am-not-getting-any-amplification.-what-might-be-causing-this
- http://localhost/pages/support/faqs/how-often-are-the-pam-sequences-presented-in-the-mammalian-genome-in-average
- http://localhost/pages/support/faqs/how-much-does-a-plate-oligo-cost-
- http://localhost/pages/support/faqs/how-long-does-it-take-to-ship-oligos-internationally
- http://localhost/pages/support/faqs/how-long-does-idt-retain-customer-orders-online-
- http://localhost/pages/support/faqs/how-does-the-efficiency-of-rna-synthesis-compare-with-dna-
- http://localhost/pages/support/faqs/how-does-idt-caclculate-extinction-coefficient-(ɛ)-and-melting-temperature-(tm)-
- http://localhost/pages/support/faqs/how-do-you-calculate-the-annealing-temperature-for-pcr-
- http://localhost/pages/support/faqs/how-do-na-and-mg-concentrations-effect-the-annealing-of-oligos-
- http://localhost/pages/support/faqs/how-do-i-use-the-oligoanalyzer-tool-to-analyze-possible-hairpins-and-dimers-formed-by-my-oligo
- http://localhost/pages/support/faqs/how-do-i-update-my-email-address-for-my-online-account-
- http://localhost/pages/support/faqs/how-do-i-separate-double-stranded-from-single-stranded-oligos-while-still-getting-good-recovery
- http://localhost/pages/support/faqs/how-do-i-resuspend-my-oligos
- http://localhost/pages/support/faqs/how-do-i-reorder-an-oligo-
- http://localhost/pages/support/faqs/how-do-i-order-sirna-oligos
- http://localhost/pages/support/faqs/how-do-i-order-sameday-oligos-
- http://localhost/pages/support/faqs/how-do-i-order-purification-on-an-oligo-
- http://localhost/pages/support/faqs/how-do-i-order-oligos-through-your-website-
- http://localhost/pages/support/faqs/how-do-i-order-modified-oligos-online-
- http://localhost/pages/support/faqs/how-do-i-order-an-oligo-with-a-modification-
- http://localhost/pages/support/faqs/how-do-i-order-a-phosphorothioate-modified-oligo-
- http://localhost/pages/support/faqs/how-do-i-order-2-o-methyl-modified-bases-on-the-website
- http://localhost/pages/support/faqs/how-do-i-input-the-include-exclude-regions-on-the-primerquest-advanced-menu-
- http://localhost/pages/support/faqs/how-do-i-find-the-price-of-individual-items-from-my-order-
- http://localhost/pages/support/faqs/how-do-i-enter-rna-sequences-online-
- http://localhost/pages/support/faqs/how-do-i-dilute-my-primers-
- http://localhost/pages/support/faqs/how-do-i-dilute-and-store-primetime-qpcr-probes-
- http://localhost/pages/support/faqs/how-do-i-determine-the-tm-of-my-sequence-
- http://localhost/pages/support/faqs/how-do-i-determine-the-number-and-cost-of-target-capture-probes-needed-to-target-n-gene-regions-on-my-ngs-custom-panel
- http://localhost/pages/support/faqs/how-do-i-determine-the-appropriate-scale-to-order-if-i-need-a-specific-amount-of-product-
- http://localhost/pages/support/faqs/how-do-i-determine-nmol-product-from-an-oligonucleotide-solution
- http://localhost/pages/support/faqs/how-do-i-design-my-gblocks-gene-fragment-for-restriction-cloning
- http://localhost/pages/support/faqs/how-do-i-choose-the-best-internal-control-target-for-normalizing-qpcr-results-
- http://localhost/pages/support/faqs/how-do-i-calculate-the-molecular-weight-of-an-oligo-
- http://localhost/pages/support/faqs/how-do-i-calculate-the-melting-temperature-of-oligos-in-salt-solutions-other-than-nacl-
- http://localhost/pages/support/faqs/how-do-5'-phosphorylated-primers-affect-pcr-
- http://localhost/pages/support/faqs/how-can-snps-affect-my-qpcr
- http://localhost/pages/support/faqs/how-can-i-verify-that-idt-received-my-order-
- http://localhost/pages/support/faqs/how-can-i-update-my-payment-information-in-my-online-account-
- http://localhost/pages/support/faqs/how-can-i-tell-if-my-oligos-successfully-annealed-
- http://localhost/pages/support/faqs/how-can-i-review-my-order-history-and-how-do-i-update-it-if-i-move-
- http://localhost/pages/support/faqs/how-can-i-pay-for-my-order-
- http://localhost/pages/support/faqs/how-can-i-order-oligos-in-a-plate-format-
- http://localhost/pages/support/faqs/how-can-i-get-around-the-purification-warning-when-ordering-on-the-website-
- http://localhost/pages/support/faqs/how-can-i-ensure-i-am-designing-my-crrna-protospacer-sequence-in-the-correct-orientation-and-to-the-appropriate-strand
- http://localhost/pages/support/faqs/how-can-i-determine-if-a-hairpin-in-my-oligo-is-too-strong-to-allow-hybridization
- http://localhost/pages/support/faqs/how-can-i-design-primers-and-probes-for-qPCR
- http://localhost/pages/support/faqs/how-can-i-concentrate-oligos-resuspended-in-water-
- http://localhost/pages/support/faqs/how-can-i-check-the-tm-of-my-oligos-
- http://localhost/pages/support/faqs/how-can-i-check-the-balance-of-my-standing-blanket-purchase-order-
- http://localhost/pages/support/faqs/how-can-i-check-my-pcr-primers-using-the-oligoanalyzer-program-to-ensure-there-are-no-significant-primer-design-issues-
- http://localhost/pages/support/faqs/how-can-i-check-my-order-status
- http://localhost/pages/support/faqs/how-can-i-adjust-the-size-of-the-amplicon-using-the-primerquest-scitools-software-
- http://localhost/pages/support/faqs/for-what-applications-is-it-ok-to-use-standard-desalted-oligos-
- http://localhost/pages/support/faqs/does-idt-offer-ned-labeled-oligos-
- http://localhost/pages/support/faqs/does-idt-have-catalog-numbers-
- http://localhost/pages/support/faqs/do-you-synthesize-custom-circular-dna-
- http://localhost/pages/support/faqs/do-you-publish-the-hplc-traces-for-hplc-purified-oligos-
- http://localhost/pages/support/faqs/do-you-provide-streptavidin-conjugated-dna-
- http://localhost/pages/support/faqs/do-you-provide-any-nonsilencing-(negative)-controls-for-dicer-substrate-rnai-duplexes-
- http://localhost/pages/support/faqs/do-you-provide-a-codon-optimization-service-
- http://localhost/pages/support/faqs/do-you-offer-fitc-labeled-primers-
- http://localhost/pages/support/faqs/do-you-have-readymade-primers-for-mouse-gapdh-
- http://localhost/pages/support/faqs/do-you-have-any-tool-to-analyze-the-restriction-enzyme-site-of-a-given-sequence
- http://localhost/pages/support/faqs/do-you-have-any-positively-charged-fluorophores-
- http://localhost/pages/support/faqs/do-you-do-post-synthesis-sequence-analysis-of-oligos-
- http://localhost/pages/support/faqs/do-the-positive-and-negative-controls-in-the-trifecta-kit-come-with-primers-and-rt-pcr-materials-
- http://localhost/pages/support/faqs/do-the-ends-of-synthetic-rna-oligos-have-the-correct-chemistry-for-ligation-
- http://localhost/pages/support/faqs/do-modifications-affect-the-stability-or-shelf-life-of-oligos
- http://localhost/pages/support/faqs/do-i-resuspend-fluorescently-labeled-oligos-the-same-as-i-would-standard-unlabeled-oligos-
- http://localhost/pages/support/faqs/do-i-need-to-have-my-oligonucleotides-purified-
- http://localhost/pages/support/faqs/do-i-need-to-anneal-dsirnas-
- http://localhost/pages/support/faqs/do-custom-oligos-come-with-5-phosphorylation-
- http://localhost/pages/support/faqs/do-annealed-double-stranded-oligos-need-to-be-modified-prior-to-ligation-into-the-appropriate-restriction-site-of-my-cloning-vector-
- http://localhost/pages/support/faqs/can-you-make-xgen-hyb-panel-probes-based-on-our-design-results-from-another-vendor
- http://localhost/pages/support/faqs/can-you-give-me-a-general-overview-of-how-you-make-your-oligos-
- http://localhost/pages/support/faqs/can-we-get-a-discounted-price-from-that-published-on-the-web-
- http://localhost/pages/support/faqs/can-the-primetime-gene-expression-master-mix-be-used-with-qpcr-probes-from-other-suppliers-(e.g.-taqman-probes-from-thermo-fisher-scientific)
- http://localhost/pages/support/faqs/can-the-primetime-gene-expression-master-mix-be-used-with-fast-cycling-conditions
- http://localhost/pages/support/faqs/can-one-order-poly-dt-and-poly-ra-from-idt-and-if-so-what-different-forms-of-purification-are-available
- http://localhost/pages/support/faqs/can-internal-nhs-ester-modifications-be-linked-to-any-base-
- http://localhost/pages/support/faqs/can-idt-synthesize-oligos-using-trimer-phosphoramidites-(trinucleotides)-
- http://localhost/pages/support/faqs/can-i-use-probes-with-iowa-black-fq-or-iowa-black-rq-on-applied-biosystems-real-time-pcr-systems-
- http://localhost/pages/support/faqs/can-i-use-hex-tet-and-6-fam-labeled-primers-in-my-multiplex-qpcr-
- http://localhost/pages/support/faqs/can-i-set-my-idt-account-to-automatically-bill-an-existing-purchase-order-
- http://localhost/pages/support/faqs/can-i-order-oligos-shorter-than-5-bases-in-length
- http://localhost/pages/support/faqs/can-i-order-my-oligos-resuspended-to-a-100um-concentration-
- http://localhost/pages/support/faqs/can-i-order-multiple-variable-regions-in-my-gblocks-gene-fragment-
- http://localhost/pages/support/faqs/can-i-order-double-stranded-oligos-
- http://localhost/pages/support/faqs/can-i-order-an-rna-oligo-modified-with-fluorophore-
- http://localhost/pages/support/faqs/can-i-get-my-25-nmol-oligos-purified-
- http://localhost/pages/support/faqs/can-i-get-custom-ratios-of-random-(mixed-degenerate)-bases-incorporated-
- http://localhost/pages/support/faqs/can-i-email-an-order-to-idt-
- http://localhost/pages/support/faqs/can-i-directly-synthesize-oligos-with-sticky-ends-rather-than-doing-a-restriction-digest-
- http://localhost/pages/support/faqs/can-i-combine-my-recently-placed-orders-to-save-on-shipping-costs-
- http://localhost/pages/support/faqs/can-i-anneal-my-dna-oligos-at-room-temperature-and-if-so-what-buffer-should-i-use-
- http://localhost/pages/support/faqs/can-gene-sequences-be-ordered-with-mixed-or-degenerate-bases-
- http://localhost/pages/support/faqs/can-dsirna-be-ordered-in-plates-
- http://localhost/pages/support/faqs/can-blast-searhes-be-performed-with-the-oligoanalyzer-program-
- http://localhost/pages/support/faqs/can-an-order-be-modified-or-cancelled-once-it-has-been-placed-
- http://localhost/pages/support/faqs/can-a-phosphorothioated-oligo-for-antisense-studies-be-used-in-medium-containing-serum-and-what-will-be-its-half-life
- http://localhost/pages/support/faqs/at-what-concentration-should-i-use-my-probes-in-my-qpcr
- http://localhost/pages/support/faqs/at-what-concentration-should-i-use-my-primers-in-my-qpcr
- http://localhost/pages/support/faqs/are-your-dicer-substrate-sirnas-(dsirnas)-provided-ready-to-use-and-do-i-need-to-order-a-transfection-reagent-separately-
- http://localhost/pages/support/faqs/are-there-deletion-products-in-a-standard-desalt-preparation-of-an-oligo
- http://localhost/pages/support/faqs/are-there-any-special-pcr-parameter-requirements-when-using-a-biotinylated-primer-
- http://localhost/pages/support/faqs/are-the-ammonium-salts-exchanged-after-page-or-hplc-purification-at-idt-
- http://localhost/pages/support/faqs/are-n-and-k-the-only-mixed-bases-are-allowed-for-gblocks-gene-fragments-
- http://localhost/pages/support/faqs/are-lyophilized-oligos-stable-when-stored-frozen-
- http://localhost/pages/support/faqs/are-idt-oligos-desalted-(salt-free)
- http://localhost/pages/support/faqs/are-idt-oligos-dnase--and-rnase-free-
- http://localhost/pages/support/faqs/are-custom-genes-delivered-as-linear-fragments-or-in-a-vector-