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Z-VAD-FMK

Cat. No. M3143

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Z-VAD-FMK Structure
Size Price Availability Quantity
1mg USD 60  USD60 In stock
5mg USD 160  USD160 In stock
10mg USD 260  USD260 In stock
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Quality Control & Documentation
Biological Activity

Z-VAD-FMK (10 μM) inhibits apoptosis in THP.1 cells. Z-VAD-FMK (10 μM) inhibits activation of PARP protease activity in control THP.1 cell lysates. Z-VAD-FMK (10 μM) inhibits the processing of CPP32 in intact THP.1 and Jurkat cells. Z-VAD-FMK (50 μM) inhibits cell death following dSMN dsRNA-induced apoptosis in S2 cells. Z-VAD-FMK (50 μM) increases the percentage of transfected cells surviving from 26% to 63% in S2 cells. Z-VAD-FMK (50 μM) blocks camptothecin-induced DNA fragmentation in HL60 cells.

Product Citations
Chemical Information
Molecular Weight 467.49
Formula C22H30FN3O7
CAS Number 187389-52-2
Solubility (25°C) DMSO ≥ 60 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Ilangovan R, et al. J Biol Chem. Inhibition of apoptosis by Z-VAD-fmk in SMN-depleted S2 cells.

[2] Slee EA, et al. Biochem J. Benzyloxycarbonyl-Val-Ala-Asp (OMe) fluoromethylketone (Z-VAD.FMK) inhibits apoptosis by blocking the processing of CPP32.

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Keywords: Z-VAD-FMK supplier, Caspase, inhibitors, activators

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