SOX2 recombinant monoclonal antibody, clone SOX2/3811R

Catalog # RAB00627

Size

Price

Stock

Quantity

Size:100 ug
Price: USD $ 479.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining of human cervical carcinoma.

  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against partial human SOX2.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Recombinant protein corresponding to amino acids 176-305 of human SOX2.

    Reactivity

    Human, Mouse

    Form

    Liquid

    Purification

    Protein A/G purification

    Isotype

    IgG

    Recommend Usage

    ELISA (Use Ab at 2-4 ug/mL for coating)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1-2 ug/mL)
    Western Blot (1-2 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 1 mg/mL PBS

    Storage Instruction

    Store at -20 to -80°C.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining of human cervical carcinoma.
  • Gene Info — SOX2

    Entrez GeneID

    6657

    Protein Accession#

    P48431

    Gene Name

    SOX2

    Gene Alias

    ANOP3, MCOPS3, MGC2413

    Gene Description

    SRY (sex determining region Y)-box 2

    Omim ID

    184429 206900

    Gene Ontology

    Hyperlink

    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

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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