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Get tips on using GeneChip® Human Genome U133 Plus 2.0 Array to perform Microarray Human - Endometrial stromal cells Expression array

Products Thermo Fisher Scientific GeneChip® Human Genome U133 Plus 2.0 Array

RNA siRNA / miRNA gene silencing Rat PC12 chorein

RNA siRNA / miRNA gene silencing Rat PC12 SOD2

RNA siRNA / miRNA gene silencing Rat PC12 Fabp5

RNA siRNA / miRNA gene silencing Rat Astrocytes PICK1

RNA siRNA / miRNA gene silencing Rat Astrocytes LRRC8A

RNA siRNA / miRNA gene silencing Rat Astrocytes Nrf2

RNA siRNA / miRNA gene silencing Rat Pericytes Cx43

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 Bacterial DNA

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

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