protein-isolation-bacteria-salmonella-typhi

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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

DNA PCR Hot start PCR Bacterial DNA

Get tips on using Ni-NTA HisSorb Strips (24) to perform Protein tag Detection of His-tagged proteins

Products Qiagen Ni-NTA HisSorb Strips (24)

Get tips on using Strep-tag Antibody (100 ug) to perform Protein tag Detection of Strep-tagged proteins

Products Qiagen Strep-tag Antibody (100 ug)

Get tips on using Ni-NTA Spin Kit (50) to perform Protein tag Detection of His-tagged proteins

Products Qiagen Ni-NTA Spin Kit (50)

Get tips on using Penta·His Alexa Fluor 647 Conjugate to perform Protein tag Detection of His-tagged proteins

Products Qiagen Penta·His Alexa Fluor 647 Conjugate

Get tips on using Ni-NTA Superflow (100 ml) to perform Protein tag Purification of His-tagged proteins

Products Qiagen Ni-NTA Superflow (100 ml)

Get tips on using RGS·His Antibody, BSA-free (100ug) to perform Protein tag Detection of His-tagged proteins

Products Qiagen RGS·His Antibody, BSA-free (100ug)

Get tips on using Penta·His Alexa Fluor 488 Conjugate to perform Protein tag Detection of His-tagged proteins

Products Qiagen Penta·His Alexa Fluor 488 Conjugate

Get tips on using QIAprep Spin Miniprep Kit to perform Plasmid Isolation Proteus mirabilis

Products Qiagen QIAprep Spin Miniprep Kit

Get tips on using GeneJET Plasmid Miniprep Kit to perform Plasmid Isolation Proteus mirabilis

Products Thermo Fisher Scientific GeneJET Plasmid Miniprep Kit

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