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Supplier : Arigo Biolaboratories
|Production type||ELISA Kits|
|Target Name||Human Factor VIII|
|Conjugation Note||TMB substrate is used for color development at 450 nm.|
|Full Name||coagulation factor VIII, procoagulant component|
|Alternate Names||Check alternative names for the Human Factor VIII (total) ELISA Kit Expand
AHF Elisa kits|Antihemophilic factor Elisa kits|Coagulation factor VIII Elisa kits|coagulation factor VIII, procoagulant component Elisa kits|coagulation factor VIIIc Elisa kits|DXS1253E Elisa kits|F8 Elisa kits|F8b Elisa kits|F8c Elisa kits|FA8_HUMAN Elisa kits|factor VIII F8B Elisa kits|Factor VIIIa light chain Elisa kits|FactorVIII Elisa kits|FVIII Elisa kits|Hema Elisa kits|Hemophilia A Elisa kits|Hemophilia, classic Elisa kits|OTTHUMP00000061446 Elisa kits|OTTHUMP00000196174 Elisa kits|Procoagulant component Elisa kits
|Storage instruction||Store the kit at 2-8°C. Keep microplate wells sealed in a dry bag with desiccants. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components or simply ask Antibodyplus for ELISA troublesooting.|
|Note||Antibodyplus and Arigo provide the most validated ELISA kits for researchers. For laboratory research only, not for drug, diagnostic or other use.|
|User’s manual of Human Factor VIII (total) ELISA Kit||Download|
|Cat No.|| |
|Conjugation note|| |
TMB substrate is used for color development at 450 nm.
|Sample type|| |
|Target name|| |
Human Factor VIII
|Store at|| |
4 Celcius degree
|Storage instruction|| |
Store the kit at 2-8 Celcius degree. Keep microplate wells sealed in a dry bag with desiccants. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components.
This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood 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. This gene produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder. [provided by RefSeq, Jul 2008]
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