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Mouse FVII / Factor VII / F7 Protein (His Tag)

Sino Biological Inc. liefert Mouse FVII / Factor VII / F7 Protein (His Tag) mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über Mouse FVII / Factor VII / F7 Protein (His Tag) lesen Sie bitte: http://www.sinobiological.com/FVII-Factor-VII-F7-Protein-g-10029.html

Produkt-Information von FVII / Factor VII / F7 Protein

Synonym AI132620, Cf7, FVII, mfVII, F7
Protein Construction

A DNA sequence encoding the mouse FⅦ  (NP_034302.2) (Met 1-Leu 446) was fused with the a polyhistidine tag at the C-terminus.

Source Mouse
Expression Host Human Cells

QC Testing von FVII / Factor VII / F7 Protein

Purity > 90 % as determined by SDS-PAGE SDS-PAGE:
SDS-PAGE

FVII protein

Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method
Stability Samples are stable for up to twelve months from date of receipt at -70℃
Predicted N terminal Val 25 & Ala 42
Molecular Mass

The mature form of mouse FⅦ consists of 416 amino acids after removal of the signal peptide and the propeptid, and has a predicted molecular mass of 47 kDa. In SDS-PAGE under reducing conditions, the apparent molecular mass of rm FⅦ is approximately 56-63 kDa due to glycosylation.

Formulation Lyophilized from sterile PBS, pH7.4.
  1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.

Usage Guide von FVII / Factor VII / F7 Protein

Storage Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

Verwandte Produkte & Themen von FVII / Factor VII / F7 Protein

Related Areas:

Enzyme>>Protease & Regulator>>Serine Protease & Regulator>>Coagulation Factor VII

Immunology>>Innate Immunity>>Coagulation>>Coagulation Factor VII

Proteins:
Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
Coagulation Factor VII Human Coagulation Factor VII/FVII/F7 Protein, Recombinant 11506-H08H
Coagulation Factor VII Mouse Coagulation Factor VII/FVII/F7 Protein, Recombinant 50034-M08C
Coagulation Factor VII Mouse FVII / Factor VII / F7 Protein, Recombinant 50034-M08S
Antibodies:
Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Mouse
Coagulation Factor VII
WB, ELISA Coagulation Factor VII Antibody, Rabbit MAb 50034-R121
Mouse
Coagulation Factor VII
WB, ELISA Rabbit Polyclonal Antibody 50034-RP01
Mouse
Coagulation Factor VII
WB, ELISA Rabbit Polyclonal Antibody (Antigen Affinity Purified) 50034-RP02

Beschreibung von FVII / Factor VII / F7 Protein

Coagulation factor VII, also known as Serum prothrombin conversion accelerator, Factor VII, F7 and FVII, is a member of the peptidase S1 family. Factor VII is one of the central proteins in the coagulation cascade. It is an enzyme of the serine protease class. Factor VII contains two EGF-like domains, one Gla (gamma-carboxy-glutamate) domain and one peptidase S1 domain. The main role of factor VII is to initiate the process of coagulation in conjunction with tissue factor (TF). Tissue factor is found on the outside of blood vessels, normally not exposed to the blood stream. The action of the Factor VII is impeded by tissue factor pathway inhibitor (TFPI), which is released almost immediately after initiation of coagulation. Factor VII is vitamin K dependent and is produced in the liver. The use of warfarin or similar anticoagulants impairs its function. Upon vessel injury, tissue factor is exposed to the blood and circulating Factor VII. Once bound to TF, FVII is activated to FVIIa by different proteases, among which are thrombin (factor IIa), factor Xa, IXa, XIIa, and the FVIIa-TF complex itself. The most important substrates for FVIIa-TF are Factor X and Factor IX.

References

  1. Kenet G. et al., 1999, Lancet. 354?(9193): 1879.
  2. Roberts H. et al., 2004, Blood. 104?(13): 3858-64.
  3. Mayer S. et al., 2005, N Engl J Med.?352?(8): 777-85.
  4. O'Connell K. et al., 2006, JAMA. 295 (3): 293-8.
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