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Rabbit anti-DLX3 polyclonal antibody - N-terminal region

Catalog Number:OM105404
OM105404
Discount Price
OM105404-100ul
1~2 Week
100ul
OM105404-50ul
50ul
OM105404-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-DLX3 polyclonal antibody - N-terminal region
Antibody Type Primary Antibodies
Antigen Alias TDO, AI4
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
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
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.
Alternative Names TDO
AI4
Molecular Weight(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/mlPositive Control: MCF7 cell lysate
Application Notes WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
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.
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