siRNA / miRNA gene silencing Mouse B16-BL6

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Get tips on using HER2/ErbB2 (29D8) Rabbit mAb #2165 to perform Western blotting HER2

Products Cell Signaling Technology HER2/ErbB2 (29D8) Rabbit mAb #2165

Get tips on using p53 Antibody (DO-1): sc-126 to perform Western blotting p53

Products Santa Cruz Biotechnology p53 Antibody (DO-1): sc-126

Get tips on using Anti-EGFR (phospho Y1068) antibody (ab5644) to perform Western blotting EGFR

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Get tips on using EGFR Antibody (E-8): sc-374607 to perform Western blotting EGFR

Products Santa Cruz Biotechnology EGFR Antibody (E-8): sc-374607

Get tips on using RNeasy Mini Kit to perform RNA isolation / purification Cells - primary human peripheral blood cells

Products Qiagen RNeasy Mini Kit

Get tips on using RNeasy Mini Kit to perform RNA isolation / purification Cells - primary human blood endothelial cell

Products Qiagen RNeasy Mini Kit

Get tips on using Qubit RNA HS Assay Kit to perform RNA quantification Fuorimetric - human blood

Products Thermo Fisher Scientific Qubit RNA HS Assay Kit

Get tips on using Quantifiler™ Duo DNA Quantification Kit to perform DNA quantification Blood

Products Thermo Fisher Scientific Quantifiler™ Duo DNA Quantification Kit

Get tips on using Quantifiler 1 Trio DNA Quantification Kit to perform DNA quantification Blood

Products Thermo Fisher Scientific Quantifiler 1 Trio DNA Quantification Kit

Protein isolation is a technique that involves isolation and/ or purification of protein from cells or tissues via chromatography or electrophoresis. The major challenges in protein isolation include: 1. The concentration of proteins in cells is variable and tends to be small for some intracellular proteins. Unlike nucleic acids, proteins cannot be amplified. 2. Proteins are more unstable than nucleic acids. They are easily denatured under suboptimal temperature, pH or salt concentrations. 3. Finally, no generalized technique/protocol can be applied for protein isolation. Proteins may have different electrostatic (number of positively or negatively charged amino acids) or hydrophobic properties. Therefore, protein purification requires multiple steps depending on their charge (a negatively charged resin/column for positively charged proteins and vice-versa), dissolution (using detergents) and unlike in the case of DNA and RNA, instead of using salts, proteins should be isolated by isoelectric precipitation.

Proteins Protein isolation Bacteria Vibrio cholerae

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