Product Information
Product Usage Information
For best results Urea Lysis Buffer should be prepared fresh prior to each experiment when working with PTMScan® protocols.
To make Urea Lysis buffer:
1. Add 45 ml of reverse osmosis deionized (RODI) or equivalent water and 10 ml of 200 mM HEPES buffer (#44686) and mix well until the urea goes completely into solution.
2. Add 1 ml of 100X stock of fresh Phosphatase Inhibitor Cocktail (#5870) just before use. Measure the volume and bring up to the final volume of 100 ml with RODI water.
Note: Dissolving urea is an endothermic reaction that decreases the temperature of the solution. This reaction will cause the urea to precipitate. Allow the solution to warm to room temperature to ensure all of the urea dissolves. The cell lysis step should take place at room temperature to prevent the urea from precipitating out of solution.
See PTMScan® protocols for additional details.
Solutions and Reagents
1X Urea lysis buffer is 9M Urea at 100 ml final volume.
Storage
Product Description
Species Reactivity
Species reactivity is determined by testing in at least one approved application (e.g., western blot).
Cross-Reactivity Key
H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected
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