產(chǎn)品詳情

  • 產(chǎn)品名稱：CathepsinB&LInhibitorZ-Phe-Phe-FMK

  • 產(chǎn)品型號：
  • 產(chǎn)品廠商：Biovision
  • 產(chǎn)品文檔：
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簡單介紹：
CathepsinB&LInhibitorZ-Phe-Phe-FMK
詳情介紹：
Sequence Z-Phe-Phe-FMK
Characteristics PubChem CID: 16760359
Molecular Formula: C??H??FN?O?
Cell Premeable: Yes
Purity > 95?% by HPLC
Chemical Name Z-FF-FMK, Cathepsin B&L Inhibitor(fluoromethylketone)
Formula C??H??FN?O?
Permeability Cell-permeable
Background Synonyms: Z-ff-FMK, Cathepsin B&L Inhibitor(fluoromethylketone)
Molecular Weight 462.5 g/mol
Application Notes The effective final concentrations of the Cathepsin B&L inhibitor is estimated to be 20-50 μ M for cell culture. However, the optimal conditions should be determined individually.
Restrictions For Research Use only
Format Liquid
Concentration 10 mM
Buffer DMSO
Handling Advice Protect from light and moisture
Storage -20 °C
Expiry Date 12 months
Supplier Images
image for Cathepsin B&L Inhibitor Z-Phe-Phe-FMK (ABIN412065) Cathepsin B&L Inhibitor Z-Phe-Phe-FMK
Product cited in: Lee, Jeong, Yoo: "Long-term incubation with proteasome inhibitors (PIs) induces IκBα degradation via the lysosomal pathway in an IκB kinase (IKK)-dependent and IKK-independent manner." in: The Journal of biological chemistry, Vol. 288, Issue 45, pp. 32777-86, 2013 (PubMed).