F8 Break Apart FISH Probe

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. [provided by RefSeq, Jul 2008]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
F8BA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
F8BA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
F8BA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
F8BA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
F8BA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
F8BA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
F8BA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
F8BA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

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. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol : F8

Gene Name : Coagulation factor VIII

Chromosome : CHR X: 155,022,722-154,835,787

Locus : Xq28

Alt. Genes : OPTN

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