Factor IX Polyclonal Antibody
规格: | / 20μL / 60μL / 120μL / 200μL |
价格: | / ¥420 / ¥1010 / ¥1640 / ¥2365 |
货号:E-AB-14396
宿主: Rabbit
反应性: H,M,R
应用: WB
Overview
Synonyms | Christmas Disease,Christmas factor,Coagulant factor IX,Coagulation factor 9,Coagulation factor IX,Coagulation factor IXa heavy chain,F9,FA9,Factor 9,Factor IX Deficiency,FactorIX,FIX,Haemophilia B,HEMB,MGC129641,MGC129642,P19,Plasma Thromboplastic Component,Plasma thromboplastin component,PTC,F9抗体 |
Swissprot | P00740 |
Source | Rabbit |
Reactivity | Human,Mouse,Rat |
Immunogen | Recombinant protein of human F9 |
Application | WB(Detection kit: E-IR-R304) |
Recommended dilution | WB,,1:500-1:2000; |
Concentration | 0.2 mg/mL |
Clonality | Polyclonal |
Properties
Cellular localization | Secreted. |
Tissue specificity | Synthesized primarily in the liver and secreted in plasma. |
Isotype | IgG |
Purification | Affinity purification |
Conjugation | Unconjugated |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
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. |