Factor VIII (clone 5E9B2), anti-human

Protein Family: Enzymes

Pathway and Disease: Immune System, Signaling Molecules and Interaction

Description:
Factor VIII, along with calcium and phospholipids, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. Defects in factor VIII are the cause of hemophilia A. Factor VIII is used to treat hemophilia A.

Alternate Names: Coagulation factor VIII, Procoagulant component, Antihemophilic factor, AHF, Factor VIIIa heavy chain, Factor VIII B chain, Factor VIIIa light chain, F8, F8C, F8B

Application Notes: E: 1:5,000-1:10,000; WB: 1:500-1:2,000

Accession No.: P00451

Antigen: Purified recombinant light chain fragment of human Factor VIII expressed in E. coli.

Format: Each vial contains 0.1 ml ascitic fluid with 0.03% sodium azide.

Storage:
Store at 4°C for short term use only. Store at -20°C for storage over 1 month. Product is guaranteed 6 months from the date of shipment.