Protein isolation Bacteria

- Found 4939 results

pcDNA-nGP1 Product

Get tips on using pcDNA-nGP1 to perform Protein Expression Eukaryotic cells - HEK293 GP1

Products Peter D. Sun, Structural Immunology Section, Laboratory of Immun pcDNA-nGP1
pcDNA-oGP1 Product

Get tips on using pcDNA-oGP1 to perform Protein Expression Eukaryotic cells - HEK293 GP1

Products Peter D. Sun, Structural Immunology Section, Laboratory of Immun pcDNA-oGP1
pMT3-RhoGC Product

Get tips on using pMT3-RhoGC to perform Protein Expression Eukaryotic cells - HEK293 RhoGC

Products Daniel D. Oprian, Dept. of Biochemistry, Brandeis University pMT3-RhoGC
pONE-40A Product

Get tips on using pONE-40A to perform Protein Expression Eukaryotic cells - HEK293 MBP

Products László Beinrohr, Institute of Enzymology, Research Centre for pONE-40A

Get tips on using PL_Mm Ppp1r15a to perform Protein Expression Eukaryotic cells - CHO Ppp1r15a

Products Helene Faustrup Kildegaard, The Novo Nordisk Foundation Center f PL_Mm Ppp1r15a
PL_Mm P4hb Product

Get tips on using PL_Mm P4hb to perform Protein Expression Eukaryotic cells - CHO P4hb

Products Helene Faustrup Kildegaard, The Novo Nordisk Foundation Center f PL_Mm P4hb
pGS-CD62L Product

Get tips on using pGS-CD62L to perform Protein Expression Eukaryotic cells - CHO CD62L

Products Peter D. Sun, Structural Immunology Section, Laboratory of Immun pGS-CD62L
pMH3-rFVII Product

Get tips on using pMH3-rFVII to perform Protein Expression Eukaryotic cells - CHO rFVII

Products Lin Peng, The Key Laboratory of Industrial Biotechnology, Minist pMH3-rFVII

Get tips on using 2-D Quant Kit to perform Protein quantification Colorimetric method

Products Sigma-Aldrich 2-D Quant Kit

A PCR reaction consists of the template DNA, two primers covering the amplification site, an enzyme, and buffers. A quantitative, real-time PCR reaction typically includes all of that plus a probe that can be detected fluorescently as the reaction runs, with no gel required. for detection. However, non-specific product amplification and primer-dimer formation during set-up are major causes of PCR failure. Nevertheless, high-quality DNA polymerase and optimize reaction buffers will certainly lead to a successful PCR reaction.

DNA PCR Conventional / Qualitative PCR bacterial DNA

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