FOXP2 polyclonal antibody (A01)

Catalog # H00093986-A01

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Size:50 uL
Price: USD $ 243.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

FOXP2 polyclonal antibody (A01), Lot # 050913JC01 Western Blot analysis of FOXP2 expression in HepG2 ( Cat # L019V1 ).

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a partial recombinant FOXP2.

    Immunogen

    FOXP2 (NP_055306, 616 a.a. ~ 715 a.a) partial recombinant protein with GST tag.

    Sequence

    LAESSLPLLSNPGLINNASSGLLQAVHEDLNGSLDHIDSNGNSSPGCSPQPHIHSIHVKEEPVIAEDEDCPMSLVTTANHSPELEDDREIEEEPLSEDLE

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Rat (61)

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Storage Buffer

    50 % glycerol

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Cell lysate)

    FOXP2 polyclonal antibody (A01), Lot # 050913JC01 Western Blot analysis of FOXP2 expression in HepG2 ( Cat # L019V1 ).

    ELISA

  • Gene Info — FOXP2

    Entrez GeneID

    93986

    GeneBank Accession#

    NM_014491

    Protein Accession#

    NP_055306

    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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