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- Custom Primers | IDT - Integrated DNA Technologies
Our custom primers and easy-to-use primer design tools help you save valuable time without sacrificing quality Reduce primer-dimers and misprimed PCR products with rhPCR primers Use with RNase H2 enzyme to increase PCR precision for accurate variant identification, microbial studies, and more
- PrimeTime™ qPCR Primer Assays - Integrated DNA Technologies
Explore IDT’s PrimeTime qPCR Primer Assays for reliable gene expression analysis Enhance your qPCR assays with high-quality, optimized primers
- rhPCR Primers | IDT - Integrated DNA Technologies
rhPCR is a novel nucleic acid amplification technology that provides improved accuracy over traditional PCR rhPCR primers (rhPrimers), unique primers that contain RNA bases, are used in conjunction with the thermostable RNase H2 enzyme to perform rhPCR
- ReadyMade™ Primers - Integrated DNA Technologies
ReadyMade Primers are stocked oligonucleotides for sample preparation, PCR, sequencing, and gene expression analysis of common genes Each primer contains 10 μg of HPLC-purified product Identity is confirmed by mass spectrometry* and purity is established by capillary electrophoresis
- Primer design tools for PCR qPCR | IDT - Integrated DNA Technologies
Simplify planning of your qPCR experiments using IDT free, online tools for oligonucleotide analysis and PCR primer design This article provides an overview of our predesigned qPCR sequences and the basics of designing customized PCR primers and hydrolysis probes with the PrimerQuest™ Tool
- Infectious Disease Innovation Unveiled at ASM 2025 | IDT
Coralville, IA (June 16, 2025)—Integrated DNA Technologies (IDT), a global genomics leader, is expanding its infectious disease portfolio with new solutions to enhance worldwide research efforts in monitoring infectious disease dynamics, supporting surveillance and accelerating biomarker discovery As part of its innovation roadmap focused on enabling academic and medical researchers, health
- How to design primers and probes for PCR and qPCR | IDT
For PCR primer design, IDT recommends that you aim for PCR primers between 18 and 30 bases; however, the most important considerations for primer design should be the T m value and on-target binding efficiency Primers should also be free of strong secondary structures and self-complementarity
- Integrated DNA Technologies | IDT
How to design primers and probes for PCR and qPCR Find everything you need to know about primer and probe design, from optimal GC content to annealing temperature READ THE ARTICLE
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