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Factor IX Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT5805
产品名称
Factor IX Rabbit Polyclonal Antibody
别名
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]
类别
常规抗体
基因名称
F9 Factor IX
蛋白名称
Factor IX
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
2158
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2158
Human Swissprot No.
P00740
Human Swissprot Link
http://www.uniprot.org/uniprotkb/P00740/entry
Mouse Gene ID
14071
Mouse Swissprot No.
P16294
Mouse Swissprot Link
http://www.uniprot.org/uniprot/P16294
Rat Swissprot No.
P16296
Rat Swissprot Link
http://www.uniprot.org/uniprot/O54941P16296
免疫原
Synthesized peptide derived from Factor IX at AA range: 412-461
特异性
Factor IX Polyclonal Antibody detects endogenous levels of Factor IX
稀释度
WB 1:500-2000, ELISA 1:10000-20000
预测分子量
52kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
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],
组织表达
Detected in blood plasma (at protein level) (PubMed:3857619, PubMed:8295821, PubMed:2592373, PubMed:9169594, PubMed:19846852). Synthesized primarily in the liver and secreted in plasma.
细胞定位
Secreted .
信号通路
Complement and coagulation cascades;
功能
catalytic activity:Selective cleavage of Arg-|-Ile bond in factor X to form factor Xa.,disease:Defects in F9 are the cause of recessive X-linked hemophilia B (HEMB) [MIM:306900]; also known as Christmas disease.,disease:Mutations in position 43 (Oxford-3, San Dimas) and 46 (Cambridge) prevents cleavage of the propeptide, mutation in position 93 (Alabama) probably fails to bind to cell membranes, mutation in position 191 (Chapel-Hill) or in position 226 (Nagoya OR Hilo) prevent cleavage of the activation peptide.,domain:Calcium binds to the gamma-carboxyglutamic acid (Gla) residues and, with stronger affinity, to another site, beyond the Gla domain.,function:Factor IX is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca(2+) ions, phospholipids, and factor VIIIa.,miscellaneous:In 1952, one of the earliest researchers of the disease, Dr. R.G. Macfarlane used the patient's surname, Christmas, to refer to the disease and also to refer to the clotting factor which he called the 'Christmas Factor' At the time Stephen Christmas was a 5-year-old boy. He died in 1993 at the age of 46 from acquired immunodeficiency syndrome contracted through treatment with blood products.,online information:Clinical information on BeneFix,online information:Factor IX entry,online information:Hemophilia B mutation database,online information:The Christmas Factor -Issue 41 of December 2003,pharmaceutical:Available under the names BeneFix (Baxter and American Home Products). Used to treat hemophilia B.,PTM:Activated by factor XIa, which excises the activation peptide.,PTM:The iron and 2-oxoglutarate dependent 3-hydroxylation of aspartate and asparagine is (R) stereospecific within EGF domains.,similarity:Belongs to the peptidase S1 family.,similarity:Contains 1 Gla (gamma-carboxy-glutamate) domain.,similarity:Contains 1 peptidase S1 domain.,similarity:Contains 2 EGF-like domains.,subunit:Heterodimer of a light chain and a heavy chain; disulfide-linked.,tissue specificity:Synthesized primarily in the liver and secreted in plasma.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Western Blot analysis of 3T3 HEPG2 cells using Factor IX Polyclonal Antibody diluted at 1:800. Secondary antibody was diluted at 1:20000

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