Anti-Factor VIII antibody [27.4] (ab41188)
Key features and details
- Mouse monoclonal [27.4] to Factor VIII
- Suitable for: ELISA, WB
- Reacts with: Human
- Isotype: IgG2a
Overview
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Product name
Anti-Factor VIII antibody [27.4]
See all Factor VIII primary antibodies -
Description
Mouse monoclonal [27.4] to Factor VIII -
Host species
Mouse -
Specificity
ab41188 does not cross react with the von Willebrand factor. -
Tested applications
Suitable for: ELISA, WBmore details -
Species reactivity
Reacts with: Human -
Immunogen
Full length native protein (purified) corresponding to Human Factor VIII (N terminal).
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Epitope
ab41188 recognises an epitope in the N-terminal region of the 83kD light chain of Factor VIII. -
General notes
This product was changed from ascites to tissue culture supernatant on 19/12/2018. Please note that the dilutions may need to be adjusted accordingly. If you have any questions please do not hesitate to contact our scientific support team.
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles. -
Storage buffer
pH: 7.40
Constituent: 99% PBS -
Concentration information loading... -
Purity
Protein G purified -
Purification notes
Purified from TCS -
Clonality
Monoclonal -
Clone number
27.4 -
Isotype
IgG2a -
Research areas
Associated products
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Assay kits
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Compatible Secondaries
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Recombinant Protein
Applications
The Abpromise guarantee
Our Abpromise guarantee covers the use of ab41188 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Abreviews | Notes |
|---|---|---|
| ELISA | ||
| WB |
| Notes |
|---|
WB: Use at an assay dependent dilution. Predicted molecular weight: 267 kDa.
Dilute in PBS or medium which is identical to that used in the assay system.
Can inhibit Factor VIII activity in coagulation assays.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Target
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Function
Factor VIII, along with calcium and phospholipid, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. -
Involvement in disease
Defects in F8 are the cause of hemophilia A (HEMA) [MIM:306700]. A disorder of blood coagulation characterized by a permanent tendency to hemorrhage. About 50% of patients have severe hemophilia resulting in frequent spontaneous bleeding into joints, muscles and internal organs. Less severe forms are characterized by bleeding after trauma or surgery. Note=Of particular interest for the understanding of the function of F8 is the category of CRM (cross-reacting material) positive patients (approximately 5%) that have considerable amount of F8 in their plasma (at least 30% of normal), but the protein is non-functional; i.e., the F8 activity is much less than the plasma protein level. CRM-reduced is another category of patients in which the F8C antigen and activity are reduced to approximately the same level. Most mutations are CRM negative, and probably affect the folding and stability of the protein. -
Sequence similarities
Belongs to the multicopper oxidase family.
Contains 3 F5/8 type A domains.
Contains 2 F5/8 type C domains.
Contains 6 plastocyanin-like domains. -
Domain
Domain F5/8 type C 2 is responsible for phospholipid-binding and essential for factor VIII activity. -
Post-translational
modificationsSulfation on Tyr-1699 is essential for binding vWF. -
Cellular localization
Secreted > extracellular space. - Information by UniProt
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Database links
- Entrez Gene: 2157 Human
- Omim: 300841 Human
- SwissProt: P00451 Human
- Unigene: 654450 Human
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Alternative names
- AHF antibody
- Antihemophilic factor antibody
- Coagulation factor VIII antibody
see all
Datasheets and documents
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Datasheet download
References (3)
ab41188 has been referenced in 3 publications.
- Gage BK et al. Generation of Functional Liver Sinusoidal Endothelial Cells from Human Pluripotent Stem-Cell-Derived Venous Angioblasts. Cell Stem Cell 27:254-269.e9 (2020). IHC-P ; Human . PubMed: 32640183
- Jankowska KI et al. Further Evidence That MicroRNAs Can Play a Role in Hemophilia A Disease Manifestation: F8 Gene Downregulation by miR-19b-3p and miR-186-5p. Front Cell Dev Biol 8:669 (2020). PubMed: 32850803
- Pandey GS et al. Detection of intracellular Factor VIII protein in peripheral blood mononuclear cells by flow cytometry. Biomed Res Int 2013:793502 (2013). PubMed: 23555096
