SHOX2 (Human) IP-WB Antibody Pair

Catalog # H00006474-PW2

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Size:1 Set
Price: USD $ 607.00
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  • +1-909-264-1399
    +1-909-992-0619
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Immunoprecipitation of SHOX2 transfected lysate using rabbit polyclonal anti-SHOX2 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-SHOX2.

  • Specification

    Product Description

    This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.

    Reactivity

    Human

    Quality Control Testing

    Immunoprecipitation-Western Blot (IP-WB)

    Immunoprecipitation of SHOX2 transfected lysate using rabbit polyclonal anti-SHOX2 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-SHOX2.

    Supplied Product

    Antibody pair set content:
    1. Antibody pair for IP: rabbit polyclonal anti-SHOX2 (300 ul)
    2. Antibody pair for WB: mouse purified polyclonal anti-SHOX2 (50 ug)

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    Immunoprecipitation-Western Blot

  • Gene Info — SHOX2

    Entrez GeneID

    6474

    Gene Name

    SHOX2

    Gene Alias

    OG12, OG12X, OGI2X, SHOT

    Gene Description

    short stature homeobox 2

    Omim ID

    602504

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq

    Other Designations

    SHOX homologous gene on chromosome 3|short stature homeobox homolog

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