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Factor VIII Polyclonal Antibody - BT-AP03124
Factor VIII Polyclonal Antibody - BT-AP03124
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Factor VIII Polyclonal Antibody
Sizes: 20μL, 50μL, 100μL
Catalogue Numbers: BT-AP03124-20, BT-AP03124-50, BT-AP03124-100
Citations, Manuals and MSDS Available upon request.
Background: F8 encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation; factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. F8 produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. DefectsF8 results in hemophilia A, a common recessive X-linked coagulation disorder.
Research Areas: Cardiovascular
Target Protein: F8
Applications: WB, IHC-p, ELISA
Reactivity: Human, Mouse
Clonality: Polyclonal
Host: Rabbit
Isotype: IgG
Full Product Name: Factor VIII Antibody
Immunogen: The antiserum was produced against synthesized peptide derived from human AMPK alpha around the phosphorylation site of Thr172. AA range:140-189
Storage: -20°C for 1 year
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Formulation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Concentration: 1 mg/ml
Molecular Weight (Da): 267009
UniProt Accession: Human: P00451; Mouse: Q06194
Synonyms: F8; F8C; Coagulation factor VIII; Antihemophilic factor; AHF; Procoagulant component
GeneID: Human: 2157; Mouse: 14069
Research Use Only
