• Product name

    Anti-Factor VIII antibody [27.4]
    See all Factor VIII primary antibodies
  • Description

    Mouse monoclonal [27.4] to Factor VIII
  • Host species

  • Specificity

    ab41188 does not cross react with the von Willebrand factor.
  • Tested applications

    Suitable for: ELISA, WBmore details
  • Species reactivity

    Reacts with: Human
  • Immunogen

    N-terminal region of the 83kD light chain of purified human Factor VIII.

  • Epitope

    ab41188 recognises an epitope in the N-terminal region of the 83kD light chain of Factor VIII.
  • General notes

    Stable for at least 1 year at -20°C to -70°C.

    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.


  • Form

  • Storage instructions

    Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
  • Storage buffer

    Preservative: None
    Constituents: PBS, pH 7.4
  • Concentration information loading...
  • Purity

    Protein G purified
  • Purification notes

    Purified from TCS
  • Clonality

  • Clone number

  • Isotype

  • Research areas


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
  • Application notes
    ELISA: 1/16,000.
    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

    • 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

      Sulfation on Tyr-1699 is essential for binding vWF.
    • Cellular localization

      Secreted > extracellular space.
    • Information by UniProt
    • Database links

    • Alternative names

      • AHF antibody
      • Antihemophilic factor antibody
      • Coagulation factor VIII antibody
      • coagulation factor VIII, procoagulant component antibody
      • coagulation factor VIIIc antibody
      • DXS1253E antibody
      • F8 antibody
      • F8b antibody
      • F8c antibody
      • FA8_HUMAN antibody
      • factor VIII F8B antibody
      • Factor VIIIa light chain antibody
      • FactorVIII antibody
      • FVIII antibody
      • Hema antibody
      • Hemophilia A antibody
      • Hemophilia, classic antibody
      • OTTHUMP00000061446 antibody
      • OTTHUMP00000196174 antibody
      • Procoagulant component antibody
      see all


    This product has been referenced in:

    • Pandey GS  et al. Detection of intracellular Factor VIII protein in peripheral blood mononuclear cells by flow cytometry. Biomed Res Int 2013:793502 (2013). Read more (PubMed: 23555096) »
    See 1 Publication for this product

    Customer reviews and Q&As

    1-3 of 3 Abreviews or Q&A


    You will receive this replacement vial tomorrow.

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    Sorry about that. I did set up the order for the correct replacement antibody, 1 vial of ab41186, but noted the wrong catalog number in the email to you.    

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    I am sorry this product did not perform as stated on the datasheet and for the inconvenience this has caused. As requested, I have issued a free of charge replacement for one vial of ab41188 with the order number 973153. To check the status of the order please contact our Customer Service team and reference this number. Please note that this free of charge replacement vial is also covered by our Abpromise guarantee. Should you still be experiencing difficulties, or if you have any further questions, please do not hesitate to let us know. I wish you the best of luck with your research.  

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