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| Product Name | Cathepsin B,L Inhibitor (Z-FF-FMK) |
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| Description | Cathepsins are localized primarily in lysosomes or endosomes, but translocated to the cytosol during apoptosis. The translocation allows these proteases to interact with caspases or other apoptosis signaling mechanisms. Studies show that cathepsins cleave certain caspases, and caspase inhibitors can inhibit cathepsin activity in vitro. Sequence: Z-Phe-Phe-FMK (FMK, fluoromethyl ketone) Purity: ≥ 95% by HPLC analysis Concentration: 10mM in DMSO Usage: The effective final concentrations of the Cathepsin B&L inhibitor is estimated to be 20-50mM for cell culture. However, the optimal conditions should be determined individually. |
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| Size | 20ul |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | n/a |
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| Gene, Accession, CAS # | n/a |
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| Catalog # | C2097-13 |
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| Order / More Info | Cathepsin B,L Inhibitor (Z-FF-FMK) from UNITED STATES BIOLOGICAL |
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| Product Specific References | n/a |
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