C1S Protein (AA 16-688) (His tag)
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- Target See all C1S Proteins
- C1S (Complement Component 1, S Subcomponent (C1S))
- Protein Type
- Recombinant
- Protein Characteristics
- AA 16-688
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This C1S protein is labelled with His tag.
- Purpose
- Human Complement Component C1s Protein
- Sequence
- Glu16-Asp688
- Characteristics
- Recombinant Human Complement Component C1s Protein is expressed from HEK293 with His tag at the C-Terminus.It contains Glu16-Asp688.
- Purity
- > 95 % as determined by Tris-Bis PAGE
- Sterility
- 0.22 μm filtered
- Endotoxin Level
- Less than 1EU per μg by the LAL method.
- Top Product
- Discover our top product C1S Protein
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- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Centrifuge the tube before opening. Reconstituting to a concentration more than 100 μg/mL is recommended. Dissolve the lyophilized protein in distilled water.
- Buffer
- Lyophilized from 0.22μm filtered solution in PBS ( pH 7.4). Normally 8 % trehalose is added as protectant before lyophilization.
- Storage
- -20 °C,-80 °C
- Storage Comment
- -20 to -80°C for 12 months as supplied from date of receipt.,-80°C for 3-6 months after reconstitution.,2-8°C for 2-7 days after reconstitution.,Recommend to aliquot the protein into smaller quantities for optimal storage. Please minimize freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- C1S (Complement Component 1, S Subcomponent (C1S))
- Alternative Name
- Complement Component C1s (C1S Products)
- Synonyms
- AA959438 Protein, AI255193 Protein, AI327365 Protein, C1sa Protein, r-gsp Protein, C1S Protein, complement C1s Protein, complement component 1, s subcomponent 1 Protein, complement component 1, s subcomponent Protein, complement component 1, s subcomponent L homeolog Protein, complement C1s subcomponent Protein, C1S Protein, C1s1 Protein, C1s Protein, c1s Protein, c1s.L Protein, LOC100558615 Protein
- Background
- Complement C1s protease inhibitors have potential utility in the treatment of diseases associated with activation of the classical complement pathway such as humorally mediated graft rejection, ischemia-reperfusion injury (IRI), vascular leak syndrome, and acute respiratory distress syndrome (ARDS).
- Molecular Weight
- 75.98 kDa. Due to enzyme lysis glycosylation, the protein migrates to 55-60 kDa (light chain), 32-35 kDa (heavy chain) and 76-96 kDa based on Tris-Bis PAGE result.
- UniProt
- P09871
- Pathways
- Complement System
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