Protein isolation Mammalian cells - Rat_Circumvallate papillae

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.

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Found 2 matching solutions for this experiment

Protocol tips
Three subcellular fractions (cytoplasmic, membrane, and nuclear) of circumvallate papillae were prepared utilizing the subcellular protein fractionation kit (Thermo Fisher Scientific, Rockford, IL, USA) and characterized by western blotting using fraction-specific protein antibodies.
RIPA Buffer

Sigma-Aldrich

Protocol tips

Excised CV (n=2/group) were incubated on ice in RIPA buffer (Sigma-Aldrich, St. Louis, MO) containing 1:100 protease inhibitor (Sigma-Aldrich), and 1:100 phosphatase inhibitor (Sigma-Aldrich) for protein isolation.
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