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The antibody against F10 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 41-300 of human F10 (NP_000495.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.
The antibody against F10 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 41-300 of human F10 (NP_000495.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.
| Cat.No | ADA-05294A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | F10 |
| Target Synonyms | FX; FXA; F10 | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.01% thimerosal, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Mouse heart, LO2, Mouse liver, OVCAR3, Rat liver | Application | ELISA, WB, IF/ICC |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 41-300 of human F10 (NP_000495.1). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | P00742 | Immunogen Sequence |
Uniprot Id
P00742
Target Species
Human
Target Name
F10
Target Full Name
Coagulation factor X
Target Function
Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of factor Va, calcium and phospholipid during blood clotting.
Target Involvement
Factor X deficiency (FA10D)
Target Subcellular Location
Secreted.
Target Protein Families
Peptidase S1 family
Target Tissue Specificity
Plasma; synthesized in the liver.
Target Research Area
Signal Transduction
Target Synonyms
Activated factor Xa heavy chain; Coagulation factor X ; F10; FA10_HUMAN; FX ; FXA; Prothrombinase ; Stuart factor; Stuart Prower factor; Stuart-Prower factor
Target Background
This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds; the light chain contains 2 EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this gene result in factor X deficiency, a hemorrhagic condition of variable severity. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides.
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