| Dilutions |
|
| Application Notes | This lysate is prepared as a positive control for separation by SDS-PAGE and subsequent Western blot analysis. Lysates are prepared in denaturing buffer WITHOUT reducing agents (i.e. 2-mercaptoethanol (BME) or dithiothreitol (DTT)). If reducing conditions are desired, add a reducing agent prior to heating. Heat lysate to 95 degrees C for 5 minutes and rapidly cool. The recommended loading amount is 0.01 mg per lane. |
| Storage | Store at -80C. Avoid freeze-thaw cycles. |
| Buffer | Triton Extraction Buffer (1 X PBS containing 0.5% Triton X 100 (v/v) and a cocktail of phosphatase and protease inhibitors) with 1 X Lithium Dodecyl Sulfate (LDS) Sample Buffer at pH 8.4. BME has not been added. |
| Preservative | 0.02% Sodium Azide |
| Concentration | 1.0 mg/ml |
The concentration calculator allows you to quickly calculate the volume, mass or concentration of your vial. Simply enter your mass, volume, or concentration values for your reagent and the calculator will determine the rest.