Protein isolation Mammalian cells - Rat_Mesenteric fat

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
Cells or tissues were harvested in ProteoJET mammalian cell lysis reagent (Fermentas Life Sciences, Ontario, Canada) or CelLytec MT mammalian tissue lysis-extraction reagent (Sigma) with proteinase inhibitor cocktail (Roche), and protein concentrations were determined with a BCA kit (Pierce, Rockford, IL).
RIPA Lysis and Extraction Buffer

Thermo Fisher Scientific

Protocol tips
The mesenteric arterioles were homogenized in radioimmunoprecipitation assay (RIPA) buffer (Thermo Fisher Scientific, Inc.) (ratio of 10 mg tissue to 100 µl RIPA buffer) with freshly added protease inhibitor, phenylmethylsulfonyl fluoride (Sigma-Aldrich; Merck Millipore, Darmstadt, Germany).
Protocol tips
The excised liver tissues or white adipose tissues (including inguinal, periovarian, mesentery, and perirenal fat) were homogenized with tissue protein reagents (T-PER, Pierce Biotechnology, Rockford, IL, USA) and equally quantified before western blotting.
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