Factor VII (F7) Mouse Monoclonal Antibody [Clone ID: RFFVII/2]
Specifications
| Product Data | |
| Clone Name | RFFVII/2 |
|---|---|
| Application | ELISA, R, WB |
| Recommended Dilution | ELISA. Clone RFFVII/2 may be used as a Capture antibody in Immunoassay for Factor VII in combination with clone RFFVII/1 as a Detection reagent. Radioimmunoassays. Western blotting: This Factor VII antibody binds to a conformational epitope and will not bind to reduced Factor VI. |
| Reactivity | Human |
| Antibody Host | Mouse |
| Isotype | IgG1 |
| Clonality | Monoclonal |
| Immunogen | Purified Factor VII. |
| Specificity | Recognizes Human Factor VII antigen. Other spcies not tested. |
| Buffer | PBS, pH 7.4 containing 0.09% Sodium Azide as preservative State: Aff - Purified State: Liquid purified IgG fraction from Tissue Culture Supernatant |
| Concentration | lot specific |
| Purification | Affinity Chromatography on Protein G |
| Conjugation | Unconjugated |
| Storage | Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
| Stability | Shelf life: one year from despatch. |
| Shipping | Blue Ice |
| Gene Name | coagulation factor VII |
| Database Link | |
| Background | Factor VII is a 50kDa multi-domain, single chain plasma glycoprotein synthesised in the liver and having anormal circulating concentration of between 400 and 600 µg/L. It is essential for blood coagulation. Factor VII is converted to the active, two chain, serine protease Factor VIIa through cleavage by thrombin, factor Xa, factor IXa or factor XIIa. Factor VIIa converts factor X to factor Xa, which in turn converts Prothrombin to Thrombin. |
| Synonyms | Proconvertin, SPCA |
| Reference Data | |
| Protein Categories | Cardiovascular diseases, Enzyme: Peptidases, Growth Factors, Secreated Proteins |
| Protein Families | Druggable Genome, Protease |
| Protein Pathways | Complement and coagulation cascades |
Reviews
Documents
| Product Manuals |
| FAQs |
| SDS |
Citations
Lee, Celik, Logsdon et al
Nat Commun (2018) 9 (1), 42 DOI: 10.1038/s41467-017-02465-5
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