C1S Protein (AA 16-688) (His tag)

N° du produit ABIN7454103

Détail du produit

Antigène: C1S (Complement Component 1, S Subcomponent (C1S))

Type de proteíne: Recombinant

Attributs du protein: AA 16-688

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette C1S protéine est marqué à la His tag.

Fonction: Human Complement Component C1s Protein

Séquence: Glu16-Asp688

Attributs du produit: Recombinant Human Complement Component C1s Protein is expressed from HEK293 with His tag at the C-Terminus.It contains Glu16-Asp688.

Pureté: > 95 % as determined by Tris-Bis PAGE

Stérilité: 0.22 μm filtered

niveau d'endotoxine: Less than 1EU per μg by the LAL method.

Information d'application

Restrictions: For Research Use only

Stockage

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.

Stock: -20 °C,-80 °C

Stockage commentaire: -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.

Date de péremption: 12 months

Détail du antigène

Antigène: C1S (Complement Component 1, S Subcomponent (C1S))

Autre désignation: Complement Component C1s (C1S Produits)

Synonymes: 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

Sujet: 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).

Poids moléculaire: 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: Système du Complément