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FA9 (heavy chain, Cleaved-Val227) rabbit pAb

FA9 (heavy chain, Cleaved-Val227) rabbit pAb

ENT-A15494

Description

 

 

 

REF ENT-A15494
Category Antibody Polyclonal
Description FA9 (heavy chain, Cleaved-Val227) rabbit pAb
Source Rabbit
Applications WB; ELISA
Reactivity Human;Mouse;Rat
Reactivity Human;Mouse;Rat
Dilution WB 1:1000-2000 ELISA 1:5000-20000
Immunogen Synthesized peptide derived from human FA9 (heavy chain, Cleaved-Val227)
Storage Stability -20°C/1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band KD 27 45kD
Human Gene ID 2158
Human Swiss Prot Nº P00740
Subcellular Location Secreted .

Other Name: Coagulation factor IX (EC 3.4.21.22;Christmas factor;Plasma thromboplastin component;PTC) [Cleaved into: Coagulation factor IXa light chain; Coagulation factor IXa heavy chain]

Background: This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. [provided by RefSeq, Sep 2015],