Factor VII anticorps

N° du produit ABIN2428811

Détail du produit anti-Factor VII anticorps

Antigène: Factor VII (F7) (Coagulation Factor VII (F7))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Factor VII est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Purification: Antigen affinity purification

Immunogène: Recombinant protein of human F7

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Conseil sur la manipulation: Avoid freeze / thaw cycles.

Stock: -20 °C/-80 °C

Stockage commentaire: Store at -20°C (regular) and -80°C (long term).

Détails sur Factor VII

Antigène: Factor VII (F7) (Coagulation Factor VII (F7))

Autre désignation: F7 (F7 Produits)

Synonymes: anticorps F7, anticorps wu:fb59f04, anticorps zgc:109870, anticorps SPCA, anticorps AI114908, anticorps ATIII, anticorps At-3, anticorps At3, anticorps LOC100223776, anticorps AI132620, anticorps Cf7, anticorps FVII, anticorps mfVII, anticorps f7, anticorps coagulation factor VII, anticorps serine (or cysteine) peptidase inhibitor, clade C (antithrombin), member 1, anticorps coagulation factor 7 (serum prothrombin conversion accelerator) S homeolog, anticorps F7, anticorps f7, anticorps Serpinc1, anticorps CpipJ_CPIJ009142, anticorps CpipJ_CPIJ010295, anticorps CpipJ_CPIJ020127, anticorps fa7, anticorps f7.S

Sujet: This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Defects in this gene can cause coagulopathy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
Synonyms: SPCA

Poids moléculaire: Calculated MW: 49 kDa

Pathways: Response to Growth Hormone Stimulus, Platelet-derived growth Factor Receptor Signaling