OK to freeze avoid repeated freeze/thaw cycles desiccated (hygroscopic) protect from light
storage temp.
−70°C
General description
A highly potent, cell-permeable, reversible, and selective inhibitor of Rho-associated protein kinases (Ki = 140 nM for p160ROCK). Also inhibits ROCK-II with equal potency. The inhibition is competitive with respect to ATP. Exhibits 10- to 50-fold lower affinity for PKCε than p160ROCK. Does not affect the activity of p21-activated protein kinase (PAK) even at higher concentrations (~100 µM). Also acts as a potent inhibitor of agonist-induced Ca2+ sensitization of myosin phosphorylation and smooth muscle contraction. Prevents apoptosis and enhances the survival and cloning efficiency of dissociated hES cells without affecting their pluripotency.
Warning
Toxicity: Irritant (B)
Physical form
A 10 mM (1 mg/296 µl) solution of Y-27632 (Cat. No. 688000)in DMSO.
Reconstitution
Following initial thaw, aliquot and freeze (-20°C).
Other Notes
Watanabe, K., et al. 2007. Nature Biotech.25, 681. Chitaley, K., et al. 2001. Nat. Med.7, 119. Davies, S.P., et al. 2000. Biochem. J. 351, 95. Narumiya, S., et al. 2000. Methods Enzymol.325, 273. Hirose, M., et al. 1998. J. Cell Biol.141, 1625. Maekawa, M., et al. 1999. Science285, 895. Uehata, M., et al. 1997. Nature389, 990.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
188.6 °F - closed cup - (Dimethylsulfoxide)
Flash Point(C)
87 °C - closed cup - (Dimethylsulfoxide)
Certificates of Analysis (COA)
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