Product Uses Include
- Inhibition of a wide range of proteases.
- Popular Activation Assay Component
MaterialProtease Inhibitor Cocktail is supplied as a white lyophilized powder. The cocktail contains the following protease inhibitors, Pepstatin A, Leupeptin, Benzamidine, Na-p-tosyl-L-arginine methyl ester (TAME). At 1X final working concentration the inhibitors are at 1 µM, 1.5 µM, 1 mM and 0.4 mM respectively.
Mode of Actionpepstatin A Reversibly inhibits some aspartic proteasesLeupeptin Reversibly inhibits trypsin like serine and some cysteine proteasesBenzamidine Inhibits serine proteasesTAME Inhibits arginine proteases, a thrombin and trypsin inhibitor
Storage and ReconstitutionLyophilized Protease Inhibitor Cocktail is stable at 4°C desiccated (<10% humidity) for 1 year.Each tube of Protease Inhibitor Cocktail should be resuspended in 1ml of DMSO (dimethyl sulfoxide) to give a 100X strength stock. The reconstituted stock can be stored at 4°C for up to 6 months or at -70°C for up to 1 year.
Related ProductsThis protease inhibitor cocktail is used in the following Cytoskeleton Activation Assays:
- Ras activation assay Biochem kit (Cat. # BK008)
- Cdc42 activation assay Biochem kit (Cat. # BK034)
- Rac activation assay Biochem kit (Cat. # BK035)
- RhoA activation assay Biochem kit (Cat. # BK036)
- G-actin : F-actin in vivo assay Biochem kit (Cat. # BK037)
- Microtubule : tubulin in vivo assay Biochem kit (Cat. # BK038)
- RhoA G-LISA™ Activation Assay Kit (luminescence) (Cat. # BK121)
- RhoA G-LISA™ Activation Assay Kit (colorimetric) (Cat. # BK124)
- Rac1,2,3 G-LISA™ Activation Assay Kit (colorimetric) (Cat. # BK125)
- Rac1 G-LISA™ Activation Assay Kit (luminescence) (Cat. # BK126)
- Cdc42 G-LISA™ Activation Assay (Cat. # BK127)
- Rac1 G-LISA™ Activation Assay (Colorimetric Based) (Cat. # BK128)
- RalA G-LISA™ Activation Assay (Colorimetric Based) (Cat. # BK129)
For product Datasheets and MSDSs please click on the PDF links below. For additional information, click on the FAQs tab above or contact our Technical Support department at tservice@cytoskeleton.com
V. Munnamalai et al. 2014. Bidirectional interactions between NOX2-type NADPH oxidase and the F-actin cytoskeleton in neuronal growth cones. J. Neurochem. doi: 10.1111/jnc.12734.
H. Vindin et al. 2013. Validation of an algorithm to quantify changes in actin cytoskeletal organization. J. Biomol. Screen. 19, 354-68.
D. Chand et al. 2012. C-terminal region of teneurin-1 co-localizes with dystroglycan and modulates cytoskeletal organization through an extracellular signal-regulated kinase-dependent stathmin- and filamin A-mediated mechanism in hippocampal cells. Neurosci. 219, 255–270.
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