Enterokinase/Enteropeptidase Antibody (N-term) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | P98073 |
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Other Accession | NP_002763 |
Clone Names | 4011211 |
Gene ID | 5651 |
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Other Names | Enteropeptidase, Enterokinase, Serine protease 7, Transmembrane protease serine 15, Enteropeptidase non-catalytic heavy chain, Enteropeptidase catalytic light chain, TMPRSS15, ENTK, PRSS7 |
Target/Specificity | The synthetic peptide sequence used to generate the antibody AP8164a was selected from the N-term region of human Enteropeptidase. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | TMPRSS15 |
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Synonyms | ENTK, PRSS7 |
Function | Responsible for initiating activation of pancreatic proteolytic proenzymes (trypsin, chymotrypsin and carboxypeptidase A). It catalyzes the conversion of trypsinogen to trypsin which in turn activates other proenzymes including chymotrypsinogen, procarboxypeptidases, and proelastases. |
Cellular Location | Membrane; Single-pass type II membrane protein |
Tissue Location | Intestinal brush border. |
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Provided below are standard protocols that you may find useful for product applications.
Background
This enzyme converts the pancreatic proenzyme trypsinogen to trypsin, which activates other proenzymes including chymotrypsinogen and procarboxypeptidases. The precursor protein is cleaved into two chains that form a heterodimer linked by a disulfide bond. This protein is a member of the trypsin family of peptidases. Mutations in this gene cause enterokinase deficiency, a malabsorption disorder characterized by diarrhea and failure to thrive.
References
Holzinger, A., et al., Am. J. Hum. Genet. 70(1):20-25 (2002).Kitamoto, Y., et al., Biochemistry 34(14):4562-4568 (1995).Kitamoto, Y., et al., Proc. Natl. Acad. Sci. U.S.A. 91(16):7588-7592 (1994).Imamura, T., et al., Am. J. Physiol. Gastrointest. Liver Physiol. 285 (6), G1235-G1241 (2003) (): ().Freeman, T.C., et al., Clin. Chim. Acta 195 (1-2), 27-39 (1990) (): ().
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