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The antibody against F12 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 336-615 of human F12 (NP_000496.2) 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 F12 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 336-615 of human F12 (NP_000496.2) 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-04541A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | F12 |
| Target Synonyms | HAF; HAE3; HAEX; F12 | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | HepG2, MCF7 | Application | ELISA, WB, IF/ICC |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 336-615 of human F12 (NP_000496.2). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | P00748 | Immunogen Sequence |
Uniprot Id
P00748
Target Species
Human
Target Name
F12
Target Full Name
Coagulation factor XII
Target Function
Factor XII is a serum glycoprotein that participates in the initiation of blood coagulation, fibrinolysis, and the generation of bradykinin and angiotensin. Prekallikrein is cleaved by factor XII to form kallikrein, which then cleaves factor XII first to alpha-factor XIIa and then trypsin cleaves it to beta-factor XIIa. Alpha-factor XIIa activates factor XI to factor XIa.
Target Involvement
Factor XII deficiency (FA12D); Hereditary angioedema 3 (HAE3)
Target Subcellular Location
Secreted.
Target Protein Families
Peptidase S1 family
Target Research Area
Cardiovascular
Target Synonyms
Factor XII; Beta factor XIIa part 1; Beta factor XIIa part 2; Coagulation factor XII; Coagulation factor XIIa heavy chain; Coagulation factor XIIa light chain; F12; F12 deficiency; FA12_HUMAN; Factor XII deficiency; HAE3; HAEX; HAF; HAF deficiency; Hageman factor
Target Background
This gene encodes coagulation factor XII which circulates in blood as a zymogen. This single chain zymogen is converted to a two-chain serine protease with an heavy chain (alpha-factor XIIa) and a light chain. The heavy chain contains two fibronectin-type domains, two epidermal growth factor (EGF)-like domains, a kringle domain and a proline-rich domain, whereas the light chain contains only a catalytic domain. On activation, further cleavages takes place in the heavy chain, resulting in the production of beta-factor XIIa light chain and the alpha-factor XIIa light chain becomes beta-factor XIIa heavy chain. Prekallikrein is cleaved by factor XII to form kallikrein, which then cleaves factor XII first to alpha-factor XIIa and then to beta-factor XIIa. The active factor XIIa participates in the initiation of blood coagulation, fibrinolysis, and the generation of bradykinin and angiotensin. It activates coagulation factors VII and XI. Defects in this gene do not cause any clinical symptoms and the sole effect is that whole-blood clotting time is prolonged.
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