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Recombinant Mouse Mast Cell Protease-1/Mcpt1 Protein, CF

R&D Systems, part of Bio-Techne | Catalog # 5146-SE

R&D Systems, part of Bio-Techne
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5146-SE-010

Key Product Details

Source

NS0

Accession #

Structure / Form

Pro form

Conjugate

Unconjugated

Applications

Enzyme Activity

Product Specifications

Source

Mouse myeloma cell line, NS0-derived mouse Mast Cell Protease-1/Mcpt1 protein
Glu19-Lys246, with a C-terminal 10-His tag

Purity

>95%, by SDS-PAGE under reducing conditions and visualized by silver stain.

Endotoxin Level

<1.0 EU per 1 μg of the protein by the LAL method.

N-terminal Sequence Analysis

Glu19

Predicted Molecular Mass

27 kDa

SDS-PAGE

33 kDa, 35 kDa and 36 kDa, reducing conditions

Activity

Measured by its ability to cleave Suc-Ala-Ala-Pro-Phe-AMC (Suc-AAPF-AMC, Bachem, Catalog # I-1465).
The specific activity is >35 pmol/min/µg, as measured under the described conditions.

Formulation, Preparation and Storage

5146-SE
Formulation Supplied as a 0.2 μm filtered solution in Tris and NaCl.
Shipping The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 6 months from date of receipt, -20 to -70 °C as supplied.
  • 3 months, -20 to -70 °C under sterile conditions after opening.

Background: Mast Cell Protease-1/Mcpt1

Mast cell protease-1 (Mcpt1), also known as beta‑chymase, is a member of the Chymase family of chymotrypsin-like serine proteases (1). mMcpt1 is a mast cell protease predominantly expressed in intestinal mucosal mast cells where it promotes mucosal permeability in intestinal allergic hypersensitivity reactions (2). Its activation is completed by the removal of a two residue N‑terminal propeptide by a dipeptidyl peptidase (Cathepsin C) (3). Like human alpha‑Chymase, Mcpt1 is capable of the conversion of angiotensin I to angiotensin II, which plays a key role in the regulation of arterial pressure (4). 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 (5, 6). Therefore, the development of specific inhibitors of chymase activity has been a pharmacologic strategy to develop therapeutic agents.

References

  1. Caughey, G.H. (2004) in Handbook of Proteolytic Enzymes (ed. Barrett, et al.), p. 1531 Academic Press, San Diego.
  2. Wastling, J.M. et al. (1998) Am. J. Pathol. 153:491.
  3. Murakami, M. et al. (1995) J. Biol. Chem. 270:2218.
  4. Saito, K. et al. (2003) Biochem. Biophys. Res. Commun. 302:773.
  5. Tsunemi, K. et al. (2004) J. Pharmacol. Exp. Ther. 309:879.
  6. Soga, Y. et al. (2004) J. Thorac. Cardiovasc. Surg. 127:72.

Alternate Names

Mast Cell Protease1, Mcp1, MMPC-1

Entrez Gene IDs

17224 (Mouse); 29265 (Rat)

Gene Symbol

MCPT1

UniProt

Additional Mast Cell Protease-1/Mcpt1 Products

Product Documents for Recombinant Mouse Mast Cell Protease-1/Mcpt1 Protein, CF

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Note: Certificate of Analysis not available for kit components.

Product Specific Notices for Recombinant Mouse Mast Cell Protease-1/Mcpt1 Protein, CF

For research use only

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