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Recombinant Mouse Serine Protease Inhibitor A3N (Serpina3n), C-His

Cat. No.AP2C751

Product TypeAnimal Proteins

Size

Product Overview

BioVenic's Recombinant Mouse Serine Protease Inhibitor A3N (Serpina3n), C-His is a recombinant protein expressed from Human Cells. Its predicted molecular weight is 46.7 kDa. The purity is>90%.

Specifications

Type Recombinant Protein
Species Mouse
Expression System Human Cells
Purity >90%
Endotoxin < 1.0 EU/μg
Predicted Molecular Weight 46.7 kDa
Physical State Lyophilized
Formulation 0.01 mol/L PBS (pH 7.2) containing 0.2% (w/v) Procline-300.

Target Information

Mouse Serine Protease Inhibitor A3N (Serpina3n) is a serine protease inhibitor involved in regulating proteolytic enzymes. In mice, Serpina3n inhibits the activity of specific proteases to prevent excessive tissue degradation and inflammation. It is implicated in various inflammatory and degenerative diseases. Serpina3n is expressed in multiple tissues and interacts with various proteases to control their activity. Its expression is regulated by inflammatory and developmental signals, making it important in both normal physiology and disease states.

Protein Mouse Serine Protease Inhibitor A3N (Serpina3n)
Protein Synonym Serpin A3N; Spi2
Gene ID 20716
UniProt ID Q91WP6

Shipping and Storage

This product is shipped with ice packs. Lyophilized protein can be stored at -20°C for 1 year. After reconstitution, the protein solution can be stored at 2-8°C for 2-7 days.

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

User Note

  1. Always centrifuge tubes before opening. Avoid mixing by vortexing or pipetting. Aliquot the reconstituted solution to minimize freeze-thaw cycles.

References

  1. Zhang, Yu. et alSerpinA3N attenuates ischemic stroke injury by reducing apoptosis and neuroinflammation. CNS neuroscience & therapeutics. 2022, 28,4: 566-579.
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