Product Description
Specifications
| Size | 25 mg, 100 mg, 1 gm |
| Accession Number | P00772 |
| Expression System | Porcine Pancreas |
| Molecular Weight (kDa) | 26.0 kDa (Bieth 2004) |
| Format | Lyophilized (powder) |
| Activity | ≥3 units per mg protein |
| Unit Definition | One Unit cleaves one micromole of N-succinyl-L-alanyl-L-alanyl-L-alanine-p-nitroanilide per minute at 25°C, pH 8.0. |
| Source | Porcine Pancreas |
| Shipping Type | Ambient temperature |
| Storage | 2-8°C |
Description
Other Information
Porcine elastase I is specific for Ala-Ala and Ala-Gly bonds, while elastase II has a broad specificity for substrates with medium to large hydrophobic amino acids in the P1 position (Gertler et al. 1977, Del Mar et al. 1980, and Gestin et al. 1997). Porcine elastase is the most potent elastase, having a rate 20-fold higher than that of human leukocyte elastase (Bieth 1978, Bieth 1986, and Largman 1983).
Hydrolysis occurs in several steps. An adsorption complex between elastase and its substrate is formed, followed by nucleophilic attack (S214) to form an acyl-enzyme intermediate, and release of the first product (the C-terminal end of the substrate). The intermediate is hydrolyzed in a deacylation step, regenerating the active enzyme and releasing the second product (Bieth 1986).
- Tissue dissociation: Because elastin is found in highest concentrations in the elastic fibers of connective tissues, elastase is frequently used to dissociate tissues that contain extensive intercellular fiber networks. For this purpose, it is usually used with other enzymes such as collagenase, trypsin, and chymotrypsin.
- Membrane protein solubilization
- Protein sequence studies


