A PCR reaction consists of the template DNA, two primers covering the amplification site, an enzyme, and buffers. However, non-specific product amplification and primer-dimer formation during set-up are major causes of PCR failure. Nevertheless, high-quality hot-start DNA polymerase and optimize reaction buffers will certainly lead to a successful PCR reaction
Get tips on using Ni-NTA HisSorb Strips (24) to perform Protein tag Detection of His-tagged proteins
Get tips on using Strep-tag Antibody (100 ug) to perform Protein tag Detection of Strep-tagged proteins
Get tips on using Ni-NTA Spin Kit (50) to perform Protein tag Detection of His-tagged proteins
Get tips on using Penta·His Alexa Fluor 647 Conjugate to perform Protein tag Detection of His-tagged proteins
Get tips on using Ni-NTA Superflow (100 ml) to perform Protein tag Purification of His-tagged proteins
Get tips on using RGS·His Antibody, BSA-free (100ug) to perform Protein tag Detection of His-tagged proteins
Get tips on using Penta·His Alexa Fluor 488 Conjugate to perform Protein tag Detection of His-tagged proteins
Get tips on using QIAprep Spin Miniprep Kit to perform Plasmid Isolation Proteus mirabilis
Get tips on using GeneJET Plasmid Miniprep Kit to perform Plasmid Isolation Proteus mirabilis
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