Protein isolation Mammalian cells - SH-SY5Y

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

Protocol tips
- Attached cells are washed three time with ice-cold PBS++ and then scraped in ice-cold PBS. Cells are transferred in microcentrifuge tubes and pelleted by centrifugation at 500 × g for 5 min.

-The rest of the protocol is performed following the manufacturer's protocol.
Protocol tips
- Cultured cells are washed with cold PBS and lysed on ice in M-PER following the manufacturer's protocol. Except, the lysate is collected and clarified by centrifugation at 12.000g for 10 min at 4°C.
CelLytic™ M

Sigma-Aldrich

Protocol tips
- Protocol was performed following the manufacturer's instructions.
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