MULTI SCIENCES
Mouse MCPT-1/mMCP-1 ELISA Kit Plate
Mouse MCPT-1/mMCP-1 ELISA Kit Plate
SKU:EK2176
Product Details
Brand | MultiSciences |
---|---|
CatNum | 70-EK2176 |
Product Name | Mouse MCPT-1/mMCP-1 ELISA Kit |
Customs Name | Mouse MCPT-1/mMCP-1 ELISA Kit |
Application | ELISA |
Reactivity | Mouse |
Assay Type | Sandwich ELISA |
Suitable Sample Type | serum, plasma, cell culture supernates |
Format | 96-well strip plate |
Storage | 4℃ (unopened) standard stored at -20℃, others stored at 4℃ (opened) |
Shipping Condition | 4℃ |
Sample Volume | 100 μl (prediluted) |
Sensitivity | 44.56 pg/ml |
Standard Curve Range | 62.50 - 4000 pg/ml |
Spike Recovery Range | 80 % - 89 % |
Mean Spike Recovery | 0.84 |
CV of Intra plate | 2.9 % - 3.9 % |
CV of Inter plate | 1.4 % - 3.5 % |
Components | 96-well polystyrene microplate coated with a monoclonal antibody against MCPT-1 Mouse MCPT-1 Standard, lyophilized MCPT-1 Detect Antibody Standard Diluent Streptavidin-HRP Assay Buffer (10×) Substrate (TMB) Stop Solution Washing Buffer (20×) Plate Covers |
Describtion | This assay employs the quantitative sandwich enzyme immunoassay technique for the quantitative detection of mouse MCPT-1. The Mouse MCPT-1/mMCP-1 ELISA is for research use only. Not for diagnostic or therapeutic procedures. Mast cell protease-1 (MCPT-1), also known as β?chymase, is a member of the Chymase family of chymotrypsin-like serine proteases and is the only chymase expressed by intestinal mucosal mast cells. Its activation is completed by the removal of a two residue N?terminal propeptide by a dipeptidyl peptidase (Cathepsin C). Like human α?Chymase, MCPT-1 is capable of the conversion of angiotensin I to angiotensin II, which plays a key role in the regulation of arterial pressure. MCPT-1 promotes mucosal permeability in intestinal allergic hypersensitivity reactions and plays an important role in host defense against intestinal parasites. Studies have shown that specific chymase inhibitors are able to diminish the development of abdominal aortic aneurysm and reduce the adhesion formation after cardiac surgery in hamsters. Therefore, the development of specific inhibitors of chymase activity has been a pharmacologic strategy to develop therapeutic agents. |
