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CASPASE-3 INHIBITOR II 1PC X 250UG
Кат. №: 264155-1MG
Производитель: Sigma-Aldrich
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Товар оформляется под заказ
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CASPASE-3 INHIBITOR II 1PC X 250UG
Main image
Кат. №: 264155-1MG
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
CASPASE-3 INHIBITOR II 1PC X 250UG
Кат. №: 264155-1MG
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description General description A potent, cell-permeable and irreversible inhibitor of CPP-32/apopain, a member of the ICE/CED-3 family of cysteine proteases. A potent, cell-permeable, and irreversible inhibitor of caspase-3 as well as caspase-6, caspase-7, caspase-8, and caspase-10. When using with purified native or recombinant enzyme, pretreatment with an esterase is required. A 5 mM (250 µg/75 µl) solution of Z-DEVD-FMK (Cat. No. 264156) in DMSO is also available. Packaging 1 mg in Plastic ampoule 250 μg in Plastic ampoule Biochem/physiol Actions Cell permeable: yes Primary Target caspase-3, caspase-6, caspase-7, caspase-8, caspase-10 Product does not compete with ATP. Reversible: no Warning Toxicity: Standard Handling (A) Sequence Z-Asp(OCH₃)-Glu(OCH₃)-Val-Asp(OCH₃)-FMK Reconstitution Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C. Other Notes Thornberry, N.A., and Lazebnik, Y. 1998. Science 281, 1312. Masuda, Y., et al. 1997. Biochem. Biophys. Res. Commun. 234, 641. Nicholson, D.W. 1996. Nature Biotech. 14, 297. Schlegel, J., et al. 1996. J. Biol. Chem. 271, 1841. Nicholson, D.W., et al. 1995. Nature 376, 37.; Description
Related Categories
A to C, Biochemicals and Reagents, Caspase, Enzyme Inhibitors, Enzyme Inhibitors by Enzyme, Enzymes, Inhibitors, and Substrates More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description General description A potent, cell-permeable and irreversible inhibitor of CPP-32/apopain, a member of the ICE/CED-3 family of cysteine proteases. A potent, cell-permeable, and irreversible inhibitor of caspase-3 as well as caspase-6, caspase-7, caspase-8, and caspase-10. When using with purified native or recombinant enzyme, pretreatment with an esterase is required. A 5 mM (250 µg/75 µl) solution of Z-DEVD-FMK (Cat. No. 264156) in DMSO is also available. Packaging 1 mg in Plastic ampoule 250 μg in Plastic ampoule Biochem/physiol Actions Cell permeable: yes Primary Target caspase-3, caspase-6, caspase-7, caspase-8, caspase-10 Product does not compete with ATP. Reversible: no Warning Toxicity: Standard Handling (A) Sequence Z-Asp(OCH₃)-Glu(OCH₃)-Val-Asp(OCH₃)-FMK Reconstitution Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C. Other Notes Thornberry, N.A., and Lazebnik, Y. 1998. Science 281, 1312. Masuda, Y., et al. 1997. Biochem. Biophys. Res. Commun. 234, 641. Nicholson, D.W. 1996. Nature Biotech. 14, 297. Schlegel, J., et al. 1996. J. Biol. Chem. 271, 1841. Nicholson, D.W., et al. 1995. Nature 376, 37.; Description
Related Categories
A to C, Biochemicals and Reagents, Caspase, Enzyme Inhibitors, Enzyme Inhibitors by Enzyme, Enzymes, Inhibitors, and Substrates More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.