
Thermo Fisher Scientific Human Factor XIIIa Native Protein
Native human Factor XIIIa protein for use as a positive control in immunological assays. Purified by SDS-PAGE, supplied in liquid form with 6.3 mg/mL concentration. Human plasma-derived, unconjugated, for in vitro research only. Stored at -20°C in 50% ...
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Applications
- Control (Ctrl): Assay-dependent
Product Specifications
| 항목 | 내용 |
|---|---|
| Species | Human |
| Molecular Weight | 312 kDa |
| Class | Native |
| Type | Protein |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 6.3 mg/mL |
| Purification | SDS-PAGE |
| Storage Buffer | 50% glycerol, 0.5M EDTA |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Wet ice |
Product Specific Information
RP-43123 contains native human Factor XIIIa protein.
It may be used as a positive control in many immunological assays.
The product is of human blood/plasma origin. Although the starting material was tested prior to initiation of the manufacturing process and found negative or nonreactive for anti-HIV-1/2, HIV-1 antigen(s), HBsAg, STS, anti-HCV, anti-HBcore, and anti-HTLV I & II, extreme caution should be used when handling this material as there is a margin of error in all tests.
This product is to be used for in vitro research purposes only, and is not intended for clinical or diagnostic use.
Target Information
This gene encodes the coagulation factor XIII A subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as plasma carrier molecules.
Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII.
This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. It also crosslinks alpha-2-plasmin inhibitor or fibronectin to the alpha chains of fibrin.
Factor XIII deficiency is classified into two categories:
- Type I deficiency: Lack of both A and B subunits
- Type II deficiency: Lack of the A subunit alone
These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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