F8 polyclonal antibody
* The price is valid only in USA. Please select country.
-
More Files
- More Functions
-
Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of F8.
Immunogen
A synthetic peptide corresponding to human F8.
Host
Rabbit
Theoretical MW (kDa)
300
Reactivity
Human, Mouse
Specificity
F8 polyclonal antibody detects endogenous levels of F8 protein.
Form
Liquid
Purification
Antigen affinity purification
Concentration
1 mg/mL
Recommend Usage
Western Blot (1:500-1:1000)
Immunohistochemistry (1:50-1:200)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (0.05% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Applications
Western Blot (Cell lysate)
Western blot analysis of HUVEC cell lysate with F8 polyclonal antibody (Cat # PAB27064).Immunohistochemistry
-
Gene Info — F8
Entrez GeneID
2157Protein Accession#
P00451Gene Name
F8
Gene Alias
AHF, DXS1253E, F8B, F8C, FVIII, HEMA
Gene Description
coagulation factor VIII, procoagulant component
Omim ID
306700Gene Ontology
HyperlinkGene Summary
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
Other Designations
OTTHUMP00000061446|OTTHUMP00000196174|coagulation factor VIII|coagulation factor VIIIc|factor VIII F8B|procoagulant component
-
Interactome
-
Pathway
-
Disease
- +1-909-264-1399
+1-909-992-0619
Toll Free : +1-877-853-6098 - +1-909-992-3401
- sales@abnova.com