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Coagulation Factor VIII / FVIII / F8 Antikörper

Produkt-Information von Coagulation Factor VIII / FVIII / F8 Antikörper

Immunogen

Recombinant Human Coagulation Factor VIII / FVIII / F8 protein

Antibody Type Rabbit Monoclonal Antibody ( Rabbit mAb Service Platform )

Clone ID

226

Ig Type

Rabbit IgG

Formulation 0.2 μm filtered solution in PBS with 5% trehalose
Preparation

This antibody was obtained from a rabbit immunized with purified, recombinant Human Coagulation Factor VIII / FVIII / F8 protein.

Usage Guide von Coagulation Factor VIII / FVIII / F8 Antikörper

Specificity

Human Coagulation Factor VIII / FVIII / F8

Western blot This antibody can be used at 1-2 μg/mL with the appropriate secondary reagents to detect Human FⅧ in WB.
Direct ELISA This antibody can be used at 0.1-0.2 μg/mL with the appropriate secondary reagents to detect Human FⅧ. The detection limit for Human FⅧ is approximately 0.078ng/well.
Storage This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -70℃. Preservative-Free.
Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.

Verwandte Produkte & Themen von Coagulation Factor VIII / FVIII / F8 Antikörper

Related Areas:
Proteins:
Antibodies:

Hintergrund von Coagulation Factor VIII / FVIII / F8 Antikörper

Coagulation Factor VIII, also known as FVIII and F8, is a member of the multicopper oxidase family. Coagulation Factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. It contains 3 F5/8 type A domains, 2 F5/8 type C domains and 6 plastocyanin-like domains. FVIII is synthesized in the liver, and perhaps in other tissues. It is a coagulation cofactor which circulates bound to von Willebrand factor and is part of the intrinsic coagulation pathway. It is a macromolecular complex composed of two separate entities, one of which, when deficient, results in hemophilia A, and the other, when deficient, results in von Willebrand's disease. Hemophilia A is a disorder of blood coagulation characterized by a permanent tendency to hemorrhage. About 50% of patients have severe hemophilia resulting in frequent spontaneous bleeding into joints, muscles and internal organs. Less severe forms are characterized by bleeding after trauma or surgery.

References

  1. Toole JJ. et al., 1984, Nature. 312(5992): 342-7.
  2. Truett MA. et al., 1985, DNA. 4(5): 333-49.
  3. Antonarakis SE. et al., 1995, Haemost. 74(1): 322-8.

Sino Biological Inc. liefert Coagulation Factor VIII / FVIII / F8 Antikörper mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über Coagulation Factor VIII / FVIII / F8 Antikörper lesen Sie bitte: http:www.sinobiological.com/Coagulation-Factor-VIII-FVIII-F8-Antibody-g-9186.html

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