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DLX3 antibody

DLX3 antibody DLX3 antibody

Instruction Manual!

Product name: DLX3 antibody
Source:Rabbit
Purity:>95%
Buffer Formulation:phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Applications:WB
Storage:Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
UOM:100ug

Rabbit anti-DLX3 polyclonal antibody - N-terminal region

Catalog Number:IC105404

Product Profile

ProductName  Rabbit anti-DLX3 polyclonal antibody - N-terminal region
AntibodyType Primary Antibodies
Immunogen
The immunogen for anti-DLX3 antibody: synthetic peptide directed towards the N terminal of human DLX3

Key Feature

Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications

WB

Species Reactivity

BovineDogGuinea PigHumanMouseRatSheep

Concentration 1mg/ml
Purification Affinity purified

Target Information

Gene Symbol DLX3
Gene Synonyms
TDO
AI4
Gene Full Name Distal-less homeobox 3
Gene Summary
DLX3 is a member of the Dlx gene family which contains 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 homeo box(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. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. 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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
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Alternative Names
TDO
AI4
MolecularWeight(MW)  32kDa
Sequence 287 amino acids

Database Links

Entrez Gene 1747
SwissProt ID O60479
Protein Accession NP_005211

Application

  • Western blot

    0.2-1 ug/ml
    Positive Control: MCF7 cell lysate

Additional Information

Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Note: The product is for research use only,not for use in diagnostic or therapeutic procedures.

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