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Calpain Inhibitor Set-Calbiochem
产品编号: | 4061649 |
规格: | The Calpain Inhibitor Set controls the biological activity of Calpain. This small molecule/inhibitor is primarily used for Protease Inhibitors applications. |
包装规格: | 1 SET |
产品类别: | 进口试剂 |
品牌: | Sigma-Aldrich |
优惠价: | 立即咨询 |
产品性质
Quality Level【质量水平】 | 100 |
form【形式】 | solid |
potency【效能】 | 8 nM Ki |
manufacturer/tradename | Calbiochem® |
storage condition【储存条件】 | OK to freeze desiccated protect from light |
shipped in【运输】 | ambient |
storage temp.【储存温度】 | −20℃ |
packaging【包装】 | 1 set in Glass bottle Packaged under inert gas |
基本信息
General description【一般描述】 | Contains 5 mg of ALLN (Cat. No. 208719), 25 mg of Calpain Inhibitor III (Cat. No. 208722), 5 mg of Calpeptin (Cat. No. 03-34-0051), 1 mg of EST (Cat. No. 330005), and 5 mg of PD 150606 (Cat. No. 513022). Calpains are a family of calcium-dependent thiol-proteases that act on a wide variety of cytoskeletal, membrane-associated, and regulatory proteins. There are two major isoforms: calpain I (µ-form) and calpain II (m-form), which differ in their calcium requirement for activation Calpains are composed of heterodimers of 80 kDa and a 30 kDa subunits. The 80 kDa unit has the catalytic site and is unique to each isozyme, whereas the 30 kDa unit is the regulatory subunit and is common to both µ- and m-isozymes. More recently, attention has been focused on the pathological significance of calcium accumulation in the central nervous system following cerebral ischemia and traumatic brain injury. Over-activation of NMDA, kainate, and AMPA receptors in the brain leads to sustained influx of Ca2+ through the voltage-gated calcium channels. Overexpression of calpains has been positively linked to both acute and chronic neurodegenerative processes including ischemia, trauma, and Alzheimer′s disease. In Alzheimer′s disease the ratio of active (76 kDa) to inactive (80 kDa) µ-calpain is reported to be much higher Calpain-dependent proteolysis is usually the late-stage common pathway towards cell death induced by excitotoxic compounds, hence, a selective inhibition of calpains to limit neuronal damage appears to be a viable therapeutic measure. |
Biochem/physiol Actions【生化/生理作用】 | Cell permeable: yes Primary Target calpain 1, calpain 2 Reversible: no |
Warning【警告】 | Toxicity: Multiple Toxicity Values, refer to MSDS (O) |
Other Notes【其他说明】 | Johnson, G.V.W., and Guttmann, R.P. 1997. BioEssays19, 1011. Kampfl, A., et al. 1997. J. Neurotauma14, 121. Sorimachi, H., et al., 1997. Biochem. J.328, 721. Bartus, R.T., et al. 1995. Neurol. Res.17, 249. Wang, K.K.W., and Yuen, P-W. 1994. Trends Pharmacol. Sci.15, 412. Saito, K., et al. 1993. Proc. Natl. Acad. Sci. USA90, 2628. Goll, D.E., et al. 1992. BioEssays14, 549. |
Legal Information【法律信息】 | CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany |
安全信息
Storage Class Code【储存分类代码】 | 11 - Combustible Solids |