You Searched For: uPA+Inhibitor+II


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Catalog Number: (77536-790)
Supplier: Bioss
Description: Bovine Tissue Inhibitors of Metalloproteinase 4 (TIMP4) ELISA Kit

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Catalog Number: (77536-608)
Supplier: Bioss
Description: Bovine Alpha-2-Plasmin Inhibitor (a2PI) ELISA Kit

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Catalog Number: (77536-784)
Supplier: Bioss
Description: Bovine Tissue Inhibitors of Metalloproteinase 1 (TIMP1) ELISA Kit

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Catalog Number: (77519-162)
Supplier: AFG Bioscience
Description: Human PTI (Placental Thrombin Inhibitor) ELISA Kit


Catalog Number: (77519-254)
Supplier: AFG Bioscience
Description: Human PIAS3 (Protein Inhibitor Of Activated STAT 3) ELISA Kit


Catalog Number: (75791-410)
Supplier: Prosci
Description: Serine protease inhibitor Kazal-type 7(SPINK7) is a secreted protein, that in humans is encoded by the SPINK7 gene. SPINK7 contains 1 Kazal-like domain. SPINK7 is probably serine protease inhibitor. Recombinant human SPINK7 is a single, non-glycosylated polypeptide chain containing 74 amino acids and fused to His-tag at c-terminus.


Catalog Number: (77516-600)
Supplier: AFG Bioscience
Description: Human BAMBI (BMP And Activin Membrane Bound Inhibitor Homolog) ELISA Kit


Catalog Number: (77517-824)
Supplier: AFG Bioscience
Description: Human LEI (Leukocyte Elastase Inhibitor) ELISA Kit


Supplier: Enzo Life Sciences
Description: Syk inhibitor

Catalog Number: (77519-506)
Supplier: AFG Bioscience
Description: Human VEGI (Vascular Endothelial Growth Inhibitor) ELISA Kit


Supplier: Enzo Life Sciences
Description: A novel NO donor which only releases NO in the presence of thiols. It is a potent vasodilator and inhibitor of platelet aggregation.

Catalog Number: (76703-986)
Supplier: AFG Bioscience
Description: Horse Plasminogen Activator Inhibitor 1(SERPINE1) ELISA Kit


Catalog Number: (89147-590)
Supplier: Enzo Life Sciences
Description: MPTP inhibitor


Supplier: Enzo Life Sciences
Description: CDK inhibitor

Catalog Number: (89156-644)
Supplier: Enzo Life Sciences
Description: A new class of proteasome inhibitors, considerably extended in comparison with the commonly used fluorescent substrates and peptide-based inhibitors, has been prepared. Evaluation of these new compounds revealed a set of highly potent proteasome inhibitors that target all individual active subunits with comparable affinity, unlike the other inhibitors described to date. These compounds are more potent in living cells than their shorter peptide vinyl sulphone counterparts. Modification of the most active compound, adamantaneacetyl-(6-aminohexanoyl)3-(leucyl)3-vinylmethyl-sulphone itself capable of proteasome inhibition in living cells, afforded a new set of radio- and affinity labels.


Supplier: Enzo Life Sciences
Description: Acyl-CoA synthetase inhibitor

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