Reagents and instruments for immunology, cell biology and molecular biology.
 
> A431 Cells, Non-Stimulated in RIPA Buffer, Sample Buffer

A431 Cells, Non-Stimulated in RIPA Buffer, Sample Buffer

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Cat# A0001-50-100ug

Size : 100ug

Brand : US Biological

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A0001-50 A431 Cells, Non-Stimulated in RIPA Buffer, Sample Buffer

Clone Type
Polyclonal
Grade
Lysate
Applications
WB
Shipping Temp
Blue Ice
Storage Temp
-20°C

Cellular protein preparation from human A431 cells||Applications:|Suitable for use in Western Blot. Other applications not tested.||Recommended Dilutions: |Add 2.5ul of 2-mercaptoethanol/100ul of lysate and boil for 5 minutes to reduce the preparation. Load 20ug of reduced lysate per lane for Western Blot analysis. This preparation may be used as a positive control for antibodies.||Storage and Stability: |May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 6 months after receipt at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.

Applications
Source: Human A431 cells|Concentration: ~1mg/ml|Form: Supplied as a liquid in RIPA diluted with non-reducing sample buffer. Cells were lysed in modified RIPA buffer (50mM Tris-HCl, pH 7.4, 1% NP40, 0.25% sodium deoxycholate, 150mM sodium chloride, 1mM EDTA, 1mM PMSF, 1ug/ml aprotinin, 1ug/ml leupeptin, 1ug/ml pepstatin, 1mM sodium orthovanadate, 1mM sodium fluoride). Diluted with non-reducing sample buffer (31mM Tris-HCl, pH 6.8, 5% glycerol, 1% SDS, 0.002% bromophenol blue).||Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Form
Supplied as a liquid in RIPA diluted with non-reducing sample buffer. Cells were lysed in modified RIPA buffer (50mM Tris-HCl, pH 7.4, 1% NP40, 0.25% sodium deoxycholate, 150mM sodium chloride, 1mM EDTA, 1mM PMSF, 1ug/ml aprotinin, 1ug/ml leupeptin, 1ug/ml pepstatin, 1mM sodium orthovanadate, 1mM sodium fluoride). Diluted with non-reducing sample buffer (31mM Tris-HCl, pH 6.8, 5% glycerol, 1% SDS, 0.002% bromophenol blue).
References
1. Dignam, J.D., et al., Nucl. Acids Res. 11: 1475-1489 (1983).