Protein isolation Mammalian cells - HepG2

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 3 matching solutions for this experiment

CelLytic™ M

Sigma-Aldrich

Protocol tips
- CellLytic M cell lysis reagent is added to the dishes and kept on ice for 5 min to lyse the cells.

- Cells are scrapped and transferred to Eppendorf tubes.
Cell Lysis Buffer (10X)

Cell Signaling Technology

Protocol tips
- Cells are washed 3 times with cold PBS and removed from the dish by scraping in cell lysis buffer supplemented with inhibitors of protease and protein phosphatase
RIPA Lysis and Extraction Buffer

Thermo Fisher Scientific

Protocol tips
- Cells were lysed in RIPA lysis buffer supplemented with complete protease inhibitor cocktail.
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