| Reactivity | HuSpecies Glossary |
| Applications | Enzyme Activity |
| Format | Carrier-Free |
| Details of Functionality | Measured by its ability to cleave a colorimetric peptide substrate, N-carbobenzyloxy-Lys-ThioBenzyl ester (Z-Lys-SBzl), in the presence of 5,5’Dithio-bis (2-nitrobenzoic acid) (DTNB). Edwards, K.M. et al. (1999) J. Biol. Chem. 274:30468. The specific activity is >20,000 pmol/min/µg, as measured under the described conditions. |
| Source | Mouse myeloma cell line, NS0-derived human Complement Component C1s protein Met1-Asp688, with a C-terminal 6-His tag |
| Accession # | |
| N-terminal Sequence | Glu16 (A chain) & Ile438 (B chain) |
| Structure / Form | Disulfide-linked heterodimer |
| Protein/Peptide Type | Recombinant Enzymes |
| Gene | C1S |
| Purity | >95%, by SDS-PAGE under reducing conditions and visualized by silver stain. |
| Endotoxin Note | <1.0 EU per 1 μg of the protein by the LAL method. |
| Dilutions |
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| Theoretical MW | 47 kDa (A chain) & 28 kDa (B chain). Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
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| SDS-PAGE | 62 kDa and 32 kDa, reducing conditions |
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| Publications |
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| Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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| Buffer | Supplied as a 0.2 μm filtered solution in Tris, NaCl, CaCl2 and Glycerol. |
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| Purity | >95%, by SDS-PAGE under reducing conditions and visualized by silver stain. |
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| Assay Procedure |
*Adjusted for Substrate Blank **Using the extinction coefficient 13260 M-1cm-1 ***Using the path correction 0.320 cm Note: the output of many spectrophotometers is in mOD Per Well:
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The classical complement pathway plays a major role in innate immunity against infection. This pathway is triggered by C1, a multimolecular complex composed of the recognition protein C1q and two serine proteases, C1r and C1s. Following the C1q recognition, C1r is autoactivated, and in turn activates C1s, which cleaves C4 and C2, the C1 substrates (1). Both C1r and C1s activation involve cleavage of a specific Arg-Ile bond, converting single-chain proenzymes into active proteases of disulfide bond-linked chains (A and B) (2). The A chains contain multiple domains in the order of CUB1-EGF-CUB2-CCP1-CCP2-Activation Peptide. The B chains contain the serine protease catalytic domain. The full-length (amino acid residues 1-688) of human C1s was expressed (3-5). The purified protein corresponded to the processed active form, with A and B chains starting at residue Glu16 and Ile438, respectively.
| Publications using 2060-SE | Applications | Species |
|---|---|---|
| X Tang, G Arora, J Matias, T Hart, Y Cui, E Fikrig A tick C1q protein alters infectivity of the Lyme disease agent by modulating interferon gamma Cell Reports, 2022-11-22;41(8):111673. 2022-11-22 [PMID: 36417869] (ELISA Capture, Bacteria - Borrelia burgdorferi (Lyme disease spirochete)) | ELISA Capture | Bacteria - Borrelia burgdorferi (Lyme disease spirochete) |
| Zhou ZH, Chen T, Arora K Complement C1 esterase inhibitor levels linked to infections and contaminated heparin-associated adverse events. PLoS ONE, 2012-04-13;7(4):e34978. 2012-04-13 [PMID: 22514695] (Binding Assay, Human) | Binding Assay | Human |
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