Factor VIII rabbit pAb
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],
Product Specifications
Background
UniProt
P00451
Swiss Prot
P00451
Reactivity
Human; Mouse
Immunogen
The antiserum was produced against synthesized peptide derived from human Factor VIII. AA range:2161-2210
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. Not yet tested in other applications.
Molecular Weight
300kD
Storage Conditions
-20°C/1 year
Product Datasheet
https://www.elkbiotech.com/upload/file/Antibodies/pAb/ES2314-1.pdf
Observed Molecular Weight
300kD
Fragment
IgG
Subcellular Location
Secreted, extracellular space.
Other Product Names
F8; F8C; Coagulation factor VIII; Antihemophilic factor; AHF; Procoagulant component
Gene ID (Human)
2157
Available Sizes
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