Factor IX Polyclonal Antibody
€0.00
In stock
SKU
E-AB-14396
Catalog Number: E-AB-14396
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: WB,ELISA
Datasheet, Questions? Contact us!
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.
Research Area: Cardiovascular, Immunology
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
Immunogen: Recombinant protein of human F9
Swissprot: P00740
Gene Accession: BC109215
Calculated MW: 52 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.2 mg/mL
Dilution: WB 1:500-1:2000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-16337
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.
Research Area: Cardiovascular, Immunology
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
Immunogen: Recombinant protein of human F9
Swissprot: P00740
Gene Accession: BC109215
Calculated MW: 52 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.2 mg/mL
Dilution: WB 1:500-1:2000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-16337
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