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HepG2 Nuclear Cell Lysate

HepG2 Nuclear Cell Lysate

Catalog Number: orb348691

DispatchUsually dispatched within 5-10 working days
$ 413.00
Catalog Numberorb348691
CategoryTools
DescriptionHepG2 Nuclear Cell Lysate
Tested applicationsChIP, IP, WB
Concentration4.0 mg/ml
Dilution rangeChIP: User Optimized, IP: User Optimized, WB: User Optimized
Form/AppearanceLiquid (sterile filtered)
PurityHep-G2 cells were grown in Eagle’s Minimum Essential Medium supplemented with 10% fetal bovine serum. Cells were washed with PBS and then incubated on ice in modified RIPA buffer, containing 150 mM sodium chloride, 50 mM Tris HCl, pH 7.4, 1 mM EDTA, 1.0% NP-40, 0.5% sodium deoxycholic acid , 0.1% SDS and 0.01% (w/v) sodium azide to lyse the cells. Protein integrity was ensured using a cocktail of protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, and serine proteases as well as aminopeptidases (0.1 mM AEBSF HCl, 0.08 µM Aprotinin, 5 µM Bestatin, 1.5 µM E-64, 2 µM Leupeptin Hemisulfate, 1 µM Pepstatin A). Phosphatase inhibitors include sodium fluoride, sodium orthovanadate, sodium pyrophosphate and β-glycerophosphate. Cell debris was removed by centrifugation. Protein concentration was determined by a modified Lowry assay using a commercially available kit. Protein concentration was adjusted to 4 mg/ml in RIPA buffer containing protease and phosphatase inhibitors.
ConjugationUnconjugated
Hazard InformationNon-Toxic
SourceHuman
StorageStore vial at -70° C or COLDER. For extended storage, aliquot Nuclear Extract to minimize freeze/thaw cycles.
Buffer/PreservativesPreservative: None. Stabilizer: None. 1X RIPA Buffer with HALT Protease and Phosphatase Inhibitors
Alternative namesHepG2 Lysate nuclear extract, cell lysate, Hep-G2
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NoteFor research use only
Application notesMulti-purpose Hep-G2 nuclear extracts are especially prepared as positive control for multiple assays including western blot, immunoprecipitation (IP), capture ELISA or other assays requiring native protein sample. For separation by SDS-PAGE and subsequent western blot analysis, lysates should be diluted by user to desired concentration in SDS-PAGE buffer with 2-mercaptoethanol or dithiothreitol as the reducing agent and heated to 95° C for 5 minutes. Sample is ready for use in immunoprecipitation and ELISA experiments, conditions should be optimized by the user. Rockland recommends its Trueblot IP reagents for immunoprecipitation experiments.
Expiration Date12 months from date of receipt.
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