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Last updated: 2017/9/17
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FOXP3 polyclonal antibody

  • Catalog # : PAB12685
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of FOXP3.
  • Immunogen:
  • A synthetic peptide corresponding to C-terminus of human FOXP3.
  • Host:
  • Rabbit
  • Theoretical MW (kDa):
  • 52
  • Reactivity:
  • Human, Mouse, Rat
  • Specificity:
  • This antibody only recognizes ~52 KDa of human FOXP3.
  • Form:
  • Liquid
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • Western Blot (0.1-1 ug/mL)
    ELISA (0.01-0.1 ug/mL)
    Immunoprecipitation (2-5 ug/mL)
    Immunohistochemistry (0.5-2 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.2 (antibody stabilizer)
  • Storage Instruction:
  • Store at 4°C. For long term storage store at -20 to -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • The HeLa cell lysate was immuno-blotted by FOXP3 polyclonal antibody (Cat # PAB12685) at 1 : 500 (Lane 1). Lane 2 was pre-incubated with immunizing peptide.
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis in human tonsil with FOXP3 polyclonal antibody (Cat # PAB12685) at 5 ug/mL.
  • Immunoprecipitation
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Immunoprecipitation
  • ELISA
  • Gene Information
  • Gene Name:
  • FOXP3
  • Gene Alias:
  • AIID,DIETER,IPEX,JM2,MGC141961,MGC141963,PIDX,XPID
  • Gene Description:
  • forkhead box P3
  • Gene Summary:
  • The protein encoded by this gene is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000025832,immune dysregulation, polyendocrinopathy, enteropathy, X-linked,immunodeficiency, polyendocrinopathy, enteropathy, X-linked,scurfin
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