Recombinant Anti-F8 (AA 1803-1818 x AA 2223-2332) Biparatopic Antibody, Tandem scFv (Clone KM41 x Clone WR8)
CAT#: VS-0525-YC80
The Recombinant Anti-F8 (AA 1803-1818 x AA 2223-2332) Biparatopic Antibody, Tandem scFv (Clone KM41 x Clone WR8) represents a biparatopic antibody (bpAb) that recognizes two discrete F8 epitopes. This bpAb, constructed as a tandem scFv, encompasses the KM41 scFv (directed against amino acids 1803-1818) N-terminally linked to the WR8 scFv (targeting amino acids 2223-2332).




Specifications
- Host Animal 1
- Human
- Host Animal 2
- Human
- Specificity
- Human factor VIII
- Species Reactivity
- Human
- Type
- Tandem scFv
- Valency
- 1 + 1
- Clone 1
- KM41
- Clone 2
- WR8
- Epitope 1
- aa 1803-1818
- Epitope 2
- aa 2223-2332
- Purity
- >90%
- Purification
- Affinity purified
- Applications
- ELISA
- Concentration
- Lot specific
- Buffer
- PBS, pH 7.4
- Preservative
- No preservatives
- Storage
- Store at 4°C for short term. Aliquot and store at -20°C for long term. Avoid freeze-thaw cycles.
- Long Name
- Coagulation Factor VIII
Target
- Introduction
- 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.
- Alternative Names
- AHF; F8B; F8C; HEMA; FVIII; DXS1253E
- Gene ID
- 2157
- UniProt ID
- P00451
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Datasheet
MSDS
COA
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