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Z-VAD-FMK (General Caspase Inhibitor)

Func, CC, BR, InhA Cell-permeable 187389-52-2 Z-VAD fluoromethylketone
Catalog No. ABIN2691062
  • Application
    Functional Studies (Func), Cell Culture (CC), Blocking Reagent (BR), Inhibition Assay (InhA)
    Purpose
    A pan-caspase inhibitor
    Brand
    BD Pharmingen™
    Sequence
    Z-Val-Ala-Asp(OMe)-FMK
    Characteristics
    Members of the caspase family play key roles in inflammation and mammalian apoptosis. Z-VAD-FMK is a cell permeable general caspase inhibitor that irreversibly binds to the catalytic site of caspase proteases and inhibits apoptosis. The peptide is O-methylated in the P1 position on aspartic acid providing enhanced stability and increased cell permeability. Z-VAD-FMK has a molecular weight of 467 Daltons. Flow cytometric analysis of apoptosis in Jurkat cells (Human T-cell leukemia, ATCC TIB-152). Jurkat cells were preincubated with the following: no inhibitor (upper left and bottom left panels), 20 μM Z-VAD-FMK (upper center and bottom center panels) or 20 μM negative control inhibitor (Z-FA-FMK, upper right and bottom right panels) (Cat. No. 550411) for 30 min, and then either left untreated (bottom row) or treated with 4 μM of campthothecin for 3 hr (top row). Following incubation, cells were collected and stained with PE Annexin V (Cat. No. 559763) to identify cells undergoing apoptosis. The results indicate that in campthothecin treated cells, approximately 42 % of the cells were induced to undergo apoptosis and the use of the general caspase inhibitor Z-VAD-FMK reduced the level of apoptosis to that observed in the untreated control. Cells treated with Z-FA-FMK (Cat. No. 550411) showed similar results to the campthothecin treated cells without inhibitor, indicating that the negative control inhibitor did not attenuate apoptosis.
    Purification
    Purified
    Chemical Name
    Z-VAD fluoromethylketone
    Formula
    C22H30N3O7F
    Permeability
    Cell-permeable
    Solubility
    DMSO
  • Comment

    BD Pharmingen™ Z-VAD-FMK, General Caspase Inhibitor – Purified
    Members of the caspase family play key roles in inflammation and mammalian apoptosis. Z-VAD-FMK is a cell permeable general caspase inhibitor that irreversibly binds to the catalytic site of caspase proteases and inhibits apoptosis. The peptide is O-methylated in the P1 position on aspartic acid providing enhanced stability and increased cell permeability. Z-VAD-FMK has a molecular weight of 467 Daltons.

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Reconstitute the Z-VAD-FMK inhibitor in DMSO before use. The reconstituted Z-VAD-FMK inhibitor may be stored in small aliquots at -20 °C.
    Storage
    -20 °C
    Storage Comment
    Avoid multiple freeze-thaws of product. Store the lyophilized Z-VAD-FMK inhibitor at -20°C. Reconstitute the Z-VAD-FMK inhibitor in DMSO before use. The reconstituted Z-VAD-FMK inhibitor may be stored in small aliquots at -20°C.
  • Gregoli, Bondurant: "Function of caspases in regulating apoptosis caused by erythropoietin deprivation in erythroid progenitors." in: Journal of cellular physiology, Vol. 178, Issue 2, pp. 133-43, (1999) (PubMed).

    Thornberry, Lazebnik: "Caspases: enemies within." in: Science (New York, N.Y.), Vol. 281, Issue 5381, pp. 1312-6, (1998) (PubMed).

  • Molecular Weight
    467 Da
    CAS-No
    187389-52-2
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