CTSK Antibody (Center E112) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | P43235 |
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Clone Names | 80513079 |
Gene ID | 1513 |
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Other Names | Cathepsin K, Cathepsin O, Cathepsin O2, Cathepsin X, CTSK, CTSO, CTSO2 |
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 | CTSK |
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Synonyms | CTSO, CTSO2 |
Function | Thiol protease involved in osteoclastic bone resorption and may participate partially in the disorder of bone remodeling. Displays potent endoprotease activity against fibrinogen at acid pH. May play an important role in extracellular matrix degradation. Involved in the release of thyroid hormone thyroxine (T4) by limited proteolysis of TG/thyroglobulin in the thyroid follicle lumen (PubMed:11082042). |
Cellular Location | Lysosome. Secreted. Apical cell membrane; Peripheral membrane protein; Extracellular side. Note=Localizes to the lumen of thyroid follicles and to the apical membrane of thyroid epithelial cells |
Tissue Location | Predominantly expressed in osteoclasts (bones) (PubMed:7805878). Expressed in thyroid epithelial cells (PubMed:11082042). |
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Provided below are standard protocols that you may find useful for product applications.
Background
The protein encoded by this gene is a lysosomal cysteineproteinase involved in bone remodeling and resorption. Thisprotein, which is a member of the peptidase C1 protein family, ispredominantly expressed in osteoclasts. However, the encodedprotein is also expressed in a significant fraction of human breastcancers, where it could contribute to tumor invasiveness. Mutationsin this gene are the cause of pycnodysostosis, an autosomalrecessive disease characterized by osteosclerosis and shortstature. This gene may be subject to RNA editing. [provided byRefSeq].
References
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)Novinec, M., et al. Biochem. J. 429(2):379-389(2010)Khan, B., et al. J. Investig. Med. 58(5):720-724(2010)Johnatty, S.E., et al. PLoS Genet. 6 (7), E1001016 (2010) :Szumilo, J., et al. Folia Histochem. Cytobiol. 47(4):571-578(2009)
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