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Recombinant Human F13a/Factor XIIIa Protein (His Tag) - PKSH033713Recombinant Human F13a Factor XIIIa Protein (His Tag) Sizes: 10g, 50g Catalogue Numbers: PKSH033713 10, PKSH033713 50 Citations, Manuals and MSDS Available upon request. Abbreviation: F13a; Factor XIIIa Target Symptom: Coagulation Factor XIII A Chain; Coagulation Factor XIIIa; Protein Glutamine Gamma Glutamyltransferase A Chain; Transglutaminase A Chain; F13A1; F13A Research Area: Tags & Cell Markers; Cardiovascular Target Species: Human Expression
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Recombinant Human F13a/Factor XIIIa Protein (His Tag)

Sizes: 10μg, 50μg

Catalogue Numbers: PKSH033713-10, PKSH033713-50

Citations, Manuals and MSDS Available upon request.

Abbreviation: F13a; Factor XIIIa

Target Symptom: Coagulation Factor XIII A Chain; Coagulation Factor XIIIa; Protein-Glutamine Gamma-Glutamyltransferase A Chain; Transglutaminase A Chain; F13A1; F13A

Research Area: Tags & Cell Markers; Cardiovascular

Target Species: Human

Expression Host: HEK293 Cells

Fusion Tag: C-His

UNIProt ID: P00488

Accession: P00488

Background: 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 composed of just 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. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion.

Sequence: Gly39-Met732

Purity: > 95 % as determined by reducing SDS-PAGE.

Formulation: Supplied as a 0.2 μm filtered solution of 50 mM NaCl, 5% Sucrose, 1% Tween 20 (v/v), 0.3% Histidine (w/v), pH8.0.
Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.

Reconstitution: Not Applicable

Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method.

Calculated MW: 80.3 kDa

Observed MW: 80-90 kDa

Storage: Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.

Shipping: This product is provided as liquid. It is shipped at frozen temperature with blue ice/gel packs. Upon receipt, store it immediately at < - 20°C.

Research Use Only

Recombinant Human F13a/Factor XIIIa Protein (His Tag) - PKSH033713

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