vWF-A2 产品
(von Willebrand Antigen 2 (vWF-A2))
Categories
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, VWDProtein level used designations for vWF-A2
- coagulation factor VIII VWF
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