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F9 monoclonal antibody, clone 13F42-F6

  • Catalog # : MAB12651
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against human F9.
  • Immunogen:
  • Native purified human F9.
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • IgG purification
  • Isotype:
  • IgG1, kappa
  • Recommend Usage:
  • ELISA
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (10 ug/mL)
    Western Blot
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In 0.05 M Na3PO4, 0.1 M NaCl, pH 6.6 (1 mM EDTA).
  • Storage Instruction:
  • Store at -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human liver with F9 monoclonal antibody, clone 13F42-F6 (Cat # MAB12651) at 10 ug/mL working concentration.
  • ELISA
  • Application Image
  • Western Blot
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 2158
  • Gene Name:
  • F9
  • Gene Alias:
  • FIX,HEMB,MGC129641,MGC129642,PTC
  • Gene Description:
  • coagulation factor IX
  • Gene Summary:
  • This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. [provided by RefSeq
  • Other Designations:
  • Christmas factor,OTTHUMP00000024154,coagulant factor IX,factor 9,factor IX,plasma thromboplastic component
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