產(chǎn)品名稱 Human Factor VIII Antibody from CREATIVE DIAGNOSTICS
產(chǎn)品貨號 CABT-L429
產(chǎn)品價格 現(xiàn)貨詢價,電話:010-67529703
產(chǎn)品規(guī)格 n/a
產(chǎn)品品牌 CREATIVE DIAGNOSTICS
產(chǎn)品概述
產(chǎn)品詳情
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Antigenic SpecificityHuman Factor VIII
Clonepolyclonal
Host SpeciesSheep
Reactive Specieshuman
Isotypen/a
Formatbiotin conjugate
Sizen/a
Concentrationn/a
ApplicationsIEP, ELISA
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DescriptionSheep Anti-Human Factor VIII polyclonal antibody for IEP, ELISA. Factor VIII (formerly referred to as antihemophilic globulin and Factor VIII:C) is a large glycoprotein (320 kDa) that circulates in plasma at approximately 200 ng/mL. Synthesized in the liver, the majority of Factor VIII is cleaved during expression, resulting in a heterogeneous mixture of partially cleaved forms of F.VIII ranging in size from 200-280 kDa. The F.VIII is stabilized by association with von Willebrand Factor to form a F.VIII-vWF complex required for the normal survival of F.VIII in vivo (t1/2 of 8-12 hours). F.VIII is a pro-cofactor that is activated through limited proteolysis by thrombin. In this process F.VIIIa dissociates from vWF to combine with activated Factor IX, calcium and a phospholipid surface where it is an essential cofactor in the assembly of the Factor X activator complex. Once dissociated from vWF, F.VIIIa is susceptible to inactivation by activated Protein C and by non-enzymatic decay. Hemophilia A is a congenital bleeding disorder resulting from an X-chromosome-linked deficiency of F.VIII. The severity of the deficiency generally correlates with the severity of the disease. Some Hemophiliacs (~10%) produce a F.VIII protein that is partially or totally inactive. The production of neutralizing antibodies to F.VIII also occurs in 5-20% of Hemophiliacs.
ImmunogenHuman F.VIII (F.VIII:C) purified from concentrate.
Other Namesn/a
Gene, Accession #Gene ID: 2157, UniProt: P00451
Catalog #CABT-L429
Price
Order / More InfoHuman Factor VIII Antibody from CREATIVE DIAGNOSTICS
Product Specific Referencesn/a
產(chǎn)品資料
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