Multiplex qPCR—how to get started

Learn how multiplex qPCR can save sample, reagent cost, and time. The article provides recommendations for multiplex qPCR assay design and experimental setup.

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Use splice junctions to your advantage in qPCR

Get recommendations for avoiding PCR amplification of genomic DNA, as well as for identifying and quantifying splice variants, in this article on designing qPCR assays that span splice junctions.

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Observing subpopulations within cloned plasmids using NGS analysis

IDT is transitioning sequence verification of our Genes products from Sanger sequencing methods to NGS. Read more to find out what the benefits are when using NGS for analysis of cloned genes.

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Planning to work with aptamers?

We are often asked whether IDT manufactures aptamers. The answer is, yes! IDT does synthesize aptamers and aptamer libraries, and there are already 100s of published research papers describing the successful use of such sequences manufactured by IDT. Learn about aptamers, SELEX, and how IDT can assist you with reagents for your aptamer applications.

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CRISPR guide RNA format affects genome editing outcomes

Learn how the use of different formats for CRISPR guide RNAs can lead to different genome editing outcomes. The optimized, short RNA oligos that make up Alt-R® CRISPR-Cas9 crRNAs and tracrRNAs outperform other CRISPR guide RNA formats. In addition to their improved editing efficiency, these short RNA oligos do not incorporate into the target genome, providing cleaner editing results by avoiding a common problem associated with DNA constructs.

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