GSC2 polyclonal antibody

Catalog # PAB17336

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Size:100 ug
Price: USD $ 346.00
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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)

Western blot analysis of extracts from 293 cells (Lane 1), HepG2 cells (Lane 2) and COLO 205 cells (Lane 3 and 4), using GSC2 polyclonal antibody (Cat # PAB17336).
Peptide "+" means "with peptide blocking".

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against synthetic peptide of GSC2.

    Immunogen

    A synthetic peptide corresponding to internal of human GSC2.

    Host

    Rabbit

    Reactivity

    Human, Mouse

    Specificity

    This antibody detects endogenous levels of total GSC2 protein.

    Form

    Liquid

    Recommend Usage

    Western Blot (1:500-1:1000)
    ELISA (1:20000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH 7.4 (150mM NaCl, 0.02% sodium azide, 50% glycerol)

    Storage Instruction

    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

    Western Blot (Cell lysate)

    Western blot analysis of extracts from 293 cells (Lane 1), HepG2 cells (Lane 2) and COLO 205 cells (Lane 3 and 4), using GSC2 polyclonal antibody (Cat # PAB17336).
    Peptide "+" means "with peptide blocking".
  • Gene Info — GSC2

    Entrez GeneID

    2928

    Protein Accession#

    O15499

    Gene Name

    GSC2

    Gene Alias

    GSCL

    Gene Description

    goosecoid homeobox 2

    Omim ID

    601845

    Gene Ontology

    Hyperlink

    Gene Summary

    Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq

    Other Designations

    goosecoid-like

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