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vWF-A2 产品

(von Willebrand Antigen 2 (vWF-A2))

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The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008].

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Recommended vWF-A2 抗体

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Application IHC, WB
Validations
Cat. No. ABIN1983485
Quantity 100 μg
Datasheet Datasheet

Recommended vWF-A2 ELISA试剂盒

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Analytical Method Quantitative Sandwich ELISA
Validations
Cat. No. ABIN4885053
Quantity 96 tests
Datasheet Datasheet
Reactivity Human
Analytical Method Semi-Quantitative Sandwich ELISA
Validations
Cat. No. ABIN6384400
Quantity 96 tests
Datasheet Datasheet

Synonyms and alternative names related to vWF-A2

von Willebrand factor (VWF), F8VWF, VWD

Protein level used designations for vWF-A2

  • coagulation factor VIII VWF
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