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SHOX2 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00006474-T01
  • Visit Frequency :
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-SHOX2 full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 39.16
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-SHOX2 antibody (H00006474-B01) by Western Blots.
    SDS-PAGE Gel
    QC Testing of H00006474-T01
    SHOX2 transfected lysate.
    Western Blot
    QC Testing of H00006474-T01
    Lane 1: SHOX2 transfected lysate ( 39.16 KDa)
    Lane 2: Non-transfected lysate.
  • Storage Buffer:
  • 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Application Image
  • Western Blot
  • Gene Information
  • Entrez GeneID:
  • 6474
  • Protein Accession#:
  • -
  • 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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