F8, Coagulation factor VIII

  • Catalog number
    IMS01-015-308
  • Price
    Please ask
  • Size
    100 µl (20 mg/ml)
  • Available ordering format
    Liquid in 0.9% NaCl, 0.1% sodium azide
  • Immunogen
    purified full length native human Coagulation Factor VIII-VWF-F VIII:c complex
  • Raised in
    Hen
  • Clonality
    Polyclonal
  • Clone
    Polyclonal
  • Purification
    Total IgY fraction
  • How to reconstitute
    See included datasheet or contact our support service
  • Storage condition
    store at 4°C; make aliquots to avoid working with a stock. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from liquid material adhering to the cap or sides of the tubes.
  • Verified applications
    immunohistochemistry (IHC), ELISA (ELISA)
  • Connected products
    IMS01-118-307 | anti-Coagulation factor VIIAS00 001 | anti-Coagulation factor VIIa AS05 058 | anti-Coagulation factor IXIMS01-137-306 | anti-Coagulation factor XIISecondary antibodies
  • Recommended dilutions for use
    1: 200 (IHC)
  • Molecular weight expected аpparent
    267 kDa
  • Verified reactivity
    human
  • Possible reactivity
    human
  • No reactivity
    no confirmed exceptions from predicted reactivity known in the moment
  • Supplementary information
    Immunohistochemistry: antibody was tested on bonin-fixed rat blood vessel.
  • References
    to be added when available
  • Scientific context
    The factor VIII complex, with a molecular weight in excess of 1 million, has 2 components: (1) factor VIII P00451 (molecular weight of 267 kDa) called factor VIII C, when measured by procoagulant activity or factor VIII Ag, when measured immunologically; (2) factor VIII R P04275 (the von Willebrand factor or vWF) has a molecular weight of 225 kDa. Factor VIII, along with calcium and phospholipids, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. Domain F5/8 type C 2 Is responsible for phospholipid binding and essential for factor VIII activity. Defects in F8 are the cause of hemophilia A (HEMA). HEMA is a common recessive X-linked coagulation disorder.
  • Notes
    IgG concentration is 22.2 µg/µl
  • Protein number
    Refer to NCBI
  • TAIR number
    Refer to NCBI
  • Description
    Aplha, transcription related growth factors and stimulating factors or repressing nuclear factors are complex subunits of proteins involved in cell differentiation. Complex subunit associated factors are involved in hybridoma growth, Eosinohils, eritroid proliferation and derived from promotor binding stimulating subunits on the DNA binding complex. NFKB 105 subunit for example is a polypetide gene enhancer of genes in B cells.
  • Gene target
  • Gene symbol
    COX8A, G3BP1, MARCHF8
  • Short name
    F8, Coagulation factor VIII
  • Alternative name
    coagulation factor VIII, procoagulant component, Coagulation factor VIII
  • Alternative to gene target
    coagulation factor VIII, procoagulant component, AHF and DXS1253E and F8B and F8C and FVIII and HEMA, F8 and IDBG-92134 and ENSG00000185010 and 2157, oxidoreductase activity, Extracellular, F8 and IDBG-157124 and ENSMUSG00000031196 and 14069, F8 and IDBG-632125 and ENSBTAG00000010726 and 100271720
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