Recombinant Human Factor XII heavy chain Protein Summary
A recombinant protein with GST tag at N-terminal corresponding to the amino acids 1-300 of Human F12 full-length ORF
Source: Wheat Germ (in vitro)
Amino Acid Sequence:MPAQPAPPKPQPTTRTPPQSQTPGALPAKREQPPSLTRNGPLSCGQRLRKSLSSMTRVVGGLVALRGAHPYIAALYWGHSFCAGSLIAPCWVLTAAHCLQDRPAPEDLTVVLGQERRNHSCEPCQTLAVRSYRLHEAFSPVSYQHDLALLRLQEDADGSCALLSPYVQPVCLPSGAARPSETTLCQVAGWGHQFEGAEEYASFLQEAQVPFLSLERCSAPDVHGSSILPGMLCAGFLEGGTDACQGDSGGPLVCEDQAAERRLTLQGIISWGSGCGDRNKPGVYTDVAYYLAWIREHTVS
|Details of Functionality
This protein is not active and should not be used for experiments requiring activity.
| Protein/Peptide Type
>80%, by SDS-PAGE
This protein has not been tested for any functionality. Product may contain endotoxins and is not suitable for use with live cells.
Packaging, Storage & Formulations
Store at -80C. Avoid freeze-thaw cycles.
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
>80%, by SDS-PAGE
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for Recombinant Human Factor XII heavy chain Protein
- beta-factor XIIa part 1
- coagulation factor XII (Hageman factor)
- coagulation factor XII
- coagulation factor XIIa heavy chain
- coagulation factor XIIa light chain
- EC 3.4.21
- EC 184.108.40.206
- HAFbeta-factor XIIa part 2
- Hageman factor
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. [provided by RefSeq]
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are guaranteed
for 3 months from date of receipt.
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