Revision 2
Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
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Product Information

Product Usage Information

1. Briefly vortex the Protease/Phosphatase Inhibitor Cocktail (100X) before use.

2. Just prior to lysing cells, dilute the cocktail 1:100 in desired lysis buffer to obtain a 1X working concentration.

Solutions and Reagents

The Protease/Phosphatase Inhibitor Cocktail (100X) is composed of a proprietary mix of Aprotinin, Bestatin, E64, and Leupeptin to promote broad spectrum protection against endogenous proteases and sodium fluoride, sodium pyrophosphate, β-glycerophosphate, and sodium orthovanadate to promote broad spectrum protection against endogenous serine/threonine and tyrosine phosphatases. The cocktail does not contain EDTA (a metalloprotease inhibitor) which can be incompatible with some downstream applications (i.e. protein assays, 2D electrophoresis, etc.). If EDTA is desired as a protease inhibitor it can be added to the cell lysis buffer at a final working concentration of 5mM.

Storage

Store the undiluted 100X cocktail at 4ºC. Do not freeze. This product is stable for 12 months.

Product Description

When diluted in lysis buffer to a final concentration of 1X the Protease/Phosphatase Inhibitor Cocktail prevents protein degradation and dephosphorylation by endogenous proteases and phosphatases present in the whole cell extract. The 100X cocktail is a clear light yellow to light green liquid.

Background

Dynamic protein phosphorylation is a key cellular signaling mechanism by which a broad spectrum of cellular processes is regulated. In order to study the phosphorylation status of specific target proteins the phosphorylated residue of interest must remain intact. When cells are lysed to make whole cell extracts, a loss of normal cellular signaling regulation occurs, and phosphatases within the cell extract are free to dephosphorylate proteins in an uncontrolled manner. The addition of phosphatase inhibitors to the cell lysis buffer aids in the preservation of phosphorylated residues at the time of cell disruption.

This same loss of normal cellular control when generating whole cell extracts also leads to uncontrolled degradation of proteins by endogenous proteases. The addition of protease inhibitors to the cell lysis buffer aids in the preservation of target proteins in the cell extract.

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

Trademarks and Patents

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

限制使用

除非 CST 的合法授书代表以书面形式书行明确同意,否书以下条款适用于 CST、其关书方或分书商提供的书品。 任何书充本条款或与本条款不同的客书条款和条件,除非书 CST 的合法授书代表以书面形式书独接受, 否书均被拒书,并且无效。

专品专有“专供研究使用”的专专或专似的专专声明, 且未专得美国食品和专品管理局或其他外国或国内专管机专专专任何用途的批准、准专或专可。客专不得将任何专品用于任何专断或治专目的, 或以任何不符合专专声明的方式使用专品。CST 专售或专可的专品提供专作专最专用专的客专,且专用于研专用途。将专品用于专断、专防或治专目的, 或专专售(专独或作专专成)或其他商专目的而专专专品,均需要 CST 的专独专可。客专:(a) 不得专独或与其他材料专合向任何第三方出售、专可、 出借、捐专或以其他方式专专或提供任何专品,或使用专品制造任何商专专品,(b) 不得复制、修改、逆向工程、反专专、 反专专专品或以其他方式专专专专专品的基专专专或技专,或使用专品开专任何与 CST 的专品或服专专争的专品或服专, (c) 不得更改或专除专品上的任何商专、商品名称、徽专、专利或版专声明或专专,(d) 只能根据 CST 的专品专售条款和任何适用文档使用专品, (e) 专遵守客专与专品一起使用的任何第三方专品或服专的任何专可、服专条款或专似专专

Revision 2
#5872

Protease/Phosphatase Inhibitor Cocktail (100X)

Protease/Phosphatase Inhibitor Cocktail (100X): Image 1 Expand Image
使用 β-Catenin (D10A8) XP® Rabbit mAb #8480 对在没有蛋白酶抑制剂(左图)或添加 Protease/Phosphatase Inhibitor Cocktail (100X) #5872(右图)的裂解缓冲液中制备且在 37ºC 下孵育规定时间点的 NIH/3T3 细胞的提取物进行蛋白质印迹分析。在没有蛋白酶抑制剂的情况下,在采集后 3 小时内,β-Catenin 信号逐渐减弱,表明蛋白被降解。在有蛋白酶抑制剂混合物的情况下,β-Catenin 降解明显减弱,并且信号在采集后 20 小时仍然存在。
Protease/Phosphatase Inhibitor Cocktail (100X): Image 2 Expand Image
使用 Phospho-Akt (Ser473) (D9E) XP® Rabbit mAb #4060(上图)或 Akt (pan) (C67E7) Rabbit mAb #4691(下图),对血清饥饿过夜、经 hPDGF-BB #8912(100ng/ml,5 分钟)处理、在没有磷酸酶抑制剂(左图)或添加 Protease/Phosphatase Inhibitor Cocktail (100X) #5872(右图)的裂解缓冲液中制备并在 37ºC 下孵育规定时间点的 NIH/3T3 细胞的提取物进行蛋白质印迹分析。在没有磷酸酶抑制剂的情况下,在时间点 0 之后,磷酸化-Akt 信号明显减弱,表明磷酸化在之后的时间点快速消失。在有磷酸酶抑制剂混合物的情况下,磷酸化-Akt 信号在所有监测的时间点中依然被保留着。