DLX3 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00001747-T02

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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

DLX3 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: DLX3 transfected lysate ( 31.70 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-DLX3 full-length

    Host

    Human

    Theoretical MW (kDa)

    31.7

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-DLX3 antibody (H00001747-D01P) by Western Blots.

    SDS-PAGE Gel

    DLX3 transfected lysate.

    Western Blot

    Lane 1: DLX3 transfected lysate ( 31.70 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 — DLX3

    Entrez GeneID

    1747

    GeneBank Accession#

    NM_005220.2

    Protein Accession#

    NP_005211.1

    Gene Name

    DLX3

    Gene Alias

    AI4, TDO

    Gene Description

    distal-less homeobox 3

    Omim ID

    104510 190320 600525

    Gene Ontology

    Hyperlink

    Gene Summary

    Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism. [provided by RefSeq

    Other Designations

    distal-less homeo box 3

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