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PCR Hot start PCR

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A PCR reaction consists of the template DNA, two primers covering the amplification site, an enzyme, and buffers. Multiplexing such a reaction amplifies the design challenges where one target requires 3 primers, which should be exclusively bound nowhere in the template DNA or to each other. Similarly, two targets require 6, three require 9, and so on. Each amplicon needs to be either a different size (for gels) or labeled with a different fluorescent tag that is spectrally distinct from the others in the reaction. Further complicating this, different targets in the reaction can compete with each other for resources and causes more challenges in the detection of amplicons. However, with proper primer designing, their validation, optimize quality and concentration of the enzyme and buffers certainly lead to a successful multiplex PCR reaction.

DNA PCR Multiplex PCR Mammalian DNA

DNA PCR Multiplex PCR Viral

DNA PCR Conventional / Qualitative PCR

Does anyone know how “strong” the PCR product of methylation specific PCR is? I kept my PCR products at 4C for about 3 weeks and then at room temperature for another week. Will I be able to use them for sequencing?

Discussions How “strong” is the PCR product of methylation specific PCR?

DNA PCR Quantitative real-time PCR

DNA PCR Multiplex PCR Poultry DNA

DNA PCR ORNi-PCR Plasmid DNA

DNA PCR Conventional / Qualitative PCR V

DNA PCR Conventional / Qualitative PCR V

DNA PCR Conventional / Qualitative PCR Vi

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