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C1S Antibody (Center) Blocking peptideSynthetic peptide
| Country | United States
Ordering Information
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|---|---|---|---|---|
| Catalog # | Size | Availability | Price | |
| BP10109c | 0.1 mg 400 ul | In Stock | $ 45.00 | DISCONTINED INQUIRE CLICK INQUIRE Add to cart |
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C1S Antibody (Center) Blocking peptide - Product info | |
| Primary Accession | P09871 |
| Other Accession | NP_958850.1, NP_001725.1 |
| Clone Names | 80902080 |
| Calculated MW | 76684 Da |
C1S Antibody (Center) Blocking peptide - Additional info | |
| Gene ID 716 | |
| Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml. | |
| 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. | |
C1S Antibody (Center) Blocking peptide - Protein Information | |
| Name C1S | |
| Function C1s B chain is a serine protease that combines with C1q and C1r to form C1, the first component of the classical pathway of the complement system. C1r activates C1s so that it can, in turn, activate C2 and C4 | |
C1S Antibody (Center) Blocking peptide - Related products
C1S Antibody (Center) Blocking peptide - Research Areas
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BACKGROUND
This gene encodes a serine protease, which is a majorconstituent of the human complement subcomponent C1. C1s associateswith two other complement components C1r and C1q in order to yieldthe first component of the serum complement system. Defects in thisgene are the cause of selective C1s deficiency. [provided byRefSeq].
REFERENCES
Han, S., et al. Hum. Immunol. 71(7):727-730(2010)Rajaraman, P., et al. Cancer Epidemiol. Biomarkers Prev. 19(5):1356-1361(2010)Pflieger, D., et al. Mol. Cell Proteomics 9(4):593-610(2010)Cerhan, J.R., et al. Br. J. Haematol. 145(5):614-623(2009)Rajaraman, P., et al. Cancer Epidemiol. Biomarkers Prev. 18(5):1651-1658(2009)