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SOX2 polyclonal antibody   

  • Catalog # : PAB12025
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  • 100 uL
  • USD $ 415
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  • Email : sales@abnova.com
    Phone : +1-909-992-0619 (new)
    Fax : +1-909-992-3401
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of SOX2.
  • Immunogen:
  • A synthetic peptide corresponding to amino acids 1-100 of human SOX2.
  • Host:
  • Rabbit
  • Reactivity:
  • Chicken, Human, Mouse, Sheep, Xenopus, Zebra fish
  • Form:
  • Liquid
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • Flow Cytometry (1:100)
    Immunocytochemistry (1:125-1:250)
    Immunofluorescence (1:50-1:200)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:125-1:250)
    Western Blot (0.5 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris-glycine, 150 mM NaCl (0.05% sodium azide)
  • Storage Instruction:
  • Store at -20°C or -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • Western blot analysis of SOX2 in mouse brain lysate with SOX2 polyclonal antibody at 0.5 ug/mL (Cat # PAB12025).
  • Immunohistochemistry
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • Immunohistochemistry
  • Gene Information
  • Entrez GeneID:
  • 6657
  • Gene Name:
  • SOX2
  • Gene Alias:
  • ANOP3,MCOPS3,MGC2413
  • Gene Description:
  • SRY (sex determining region Y)-box 2
  • Gene Summary:
  • This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq
  • Other Designations:
  • SRY-related HMG-box gene 2,sex-determining region Y-box 2,transcription factor SOX2
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