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Last updated: 2016/12/4
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SHOX2 MaxPab rabbit polyclonal antibody (D01)MaxPab

  • Catalog # : H00006474-D01
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against a full-length human SHOX2 protein.
  • Immunogen:
  • SHOX2 (AAH08829.1, 1 a.a. ~ 355 a.a) full-length human protein.
  • Sequence:
  • MEELTAFVSKSFDQKVKEKKEAITYREVLESGPLRGAKEPTGCTEAGRDDRSSPAVRAAGGGGGGGGGGGGGGGGGGVGGGGAGGGAGGGRSPVRELDMGAAERSREPGSPRLTEGRRKPTKAEVQATLLLPGEAFRFLVSPELKDRKEDAKGMEDEGQTKIKQRRSRTNFTLEQLNELERLFDETHYPDAFMREELSQRLGLSEARVQVWFQNRRAKCRKQENQLHKGVLIGAASQFEACRVAPYVNVGALRMPFQQDSHCNVTPLSFQVQAQLQLDSAVAHAHHHLHPHLAAHAPYMMFPAPPFGLPLATLAADSASAASVVAAAAAAKTTSKNSSIADLRLKAKKHAAALGL
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody reactive against mammalian transfected lysate.
  • Storage Buffer:
  • No additive
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Immunoprecipitation
  • Immunoprecipitation
  • Immunoprecipitation of SHOX2 transfected lysate using anti-SHOX2 MaxPab rabbit polyclonal antibody and Protein A Magnetic Bead (U0007), and immunoblotted with SHOX2 purified MaxPab mouse polyclonal antibody (B01P) (H00006474-B01P).
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  • Gene Information
  • Entrez GeneID:
  • 6474
  • Gene Name:
  • SHOX2
  • Gene Alias:
  • OG12,OG12X,OGI2X,SHOT
  • Gene Description:
  • short stature homeobox 2
  • 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
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