FOXP2 monoclonal antibody, clone 5C11A2

Catalog # MAB17708

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Size:100 uL
Price: USD $ 531.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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Enzyme-linked Immunoabsorbent Assay
Application

Enzyme-linked Immunoabsorbent Assay

ELISA analysis of FOXP2 monoclonal antibody, clone 5C11A2.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against recombinant human FOXP2.

    Immunogen

    Recombinant protein corresponding to human FOXP2 from E. coli.

    Host

    Mouse

    Theoretical MW (kDa)

    85

    Reactivity

    Human

    Form

    Liquid

    Isotype

    IgG1

    Recommend Usage

    ELISA (1:10000)
    Flow Cytometry
    Immunocytochemistry
    Immunohistochemistry
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In ascites (0.03% sodium azide).

    Storage Instruction

    Store at 4°C. For long term storage store at -20°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

    Enzyme-linked Immunoabsorbent Assay

    ELISA analysis of FOXP2 monoclonal antibody, clone 5C11A2.
  • Gene Info — FOXP2

    Entrez GeneID

    93986

    Gene Name

    FOXP2

    Gene Alias

    CAGH44, DKFZp686H1726, SPCH1, TNRC10

    Gene Description

    forkhead box P2

    Omim ID

    602081 605317

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes an evolutionarily conserved transcription factor expressed in fetal and adult brain. This transcription factor is a member of the forkhead/winged-helix (FOX) family of transcription factors, and contains a FOX DNA-binding domain and a large polyglutamine tract. Members of the FOX family of transcription factors are regulators of embryogenesis. The product of this gene is thought to be required for proper development of speech and language regions of the brain during embryogenesis. Although a point mutation in this gene has been associated with the KE pedigree segregating developmental verbal dyspraxia, no association between mutations in this gene and another speech disorder, autism, has been found. Multiple alternative transcripts encoding different isoforms have been identified. [provided by RefSeq

    Other Designations

    CAG repeat protein 44|OTTHUMP00000067772|forkhead/winged-helix transcription factor|speech and language disorder 1|trinucleotide repeat containing 10

  • 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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