Technical Data
A0001-50
A431 Cells, Non-Stimulated in RIPA Buffer, Sample Buffer
100ul
|
Technical Data |
|
A0001-50 |
A431 Cells, Non-Stimulated in RIPA Buffer, Sample Buffer |
100ul |
| Cells, Lysates, Plasma, Serum, Tissues | Storage: -20°CShipping: Blue Ice |
|
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 at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. |
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. |
|
1. Dignam, J.D., et al., Nucl. Acids Res. 11: 1475-1489 (1983).
|
||