SHOX2 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00006474-T01

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Size:100 uL
Price: USD $ 247.00
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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
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

SHOX2 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: SHOX2 transfected lysate ( 39.16 KDa)
Lane 2: Non-transfected lysate.

  • 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

    SHOX2 transfected lysate.

    Western Blot

    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

  • Gene Info — SHOX2

    Entrez GeneID

    6474

    GeneBank Accession#

    BC008829.2

    Protein Accession#

    -

    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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