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Antibody detects endogenous levels of total Factor VIII.
This gene 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. This gene 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. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: AHF; Antihemophilic factor; Coagulation factor VIII; coagulation factor VIII A1 domain; coagulation factor VIII C2 domain; coagulation factor VIII, procoagulant component; coagulation factor VIIIc; Factor 8; Factor VIII; factor VIII F8B; factor8; Procoagulant component; RP11-115M6.7
基因别名: AHF; Cf-8; Cf8; DXS1253E; F8; F8B; F8C; FVIII; HEMA
UniProt ID: (Mouse) Q06194, (Human) P00451
Entrez Gene ID: (Rat) 302470, (Mouse) 14069, (Human) 2157