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Dlx-3 Polyclonal Antibody

Polyclonal antibody

Specification

BYab-15752

  • 50UL $180 100UL $255
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Host
Reactiveness
Use
Molecular weight (DA)
45kD
Immunogen
The antiserum was produced against synthesized peptide derived from human DLX3. AA range:71-120
Specificity
Dlx-3 Polyclonal Antibody detects endogenous levels of Dlx-3 protein.
Source
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Dilution rate
WB: 1/500 - 1/2000. IHC: 1/100 - 1/300. ELISA: 1/40000.. IF 1:50-200
Purification process (Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1 mg/ml
Background
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, Jul 2008],
Function
disease:Defects in DLX3 are a cause of trichodentoosseous syndrome (TDO) [MIM:190320]. TDO is an autosomal dominant syndrome characterized by enamel hypoplasia and hypocalcification with associated strikingly curly hair.,disease:Defects in DLX3 are the cause of amelogenesis imperfecta type 4 (AI4) [MIM:104510]; also known as amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism. AI4 is an autosomal dominant defect of enamel formation associated with enlarged pulp chambers.,function:Likely to play a regulatory role in the development of the ventral forebrain. May play a role in craniofacial patterning and morphogenesis.,similarity:Belongs to the distal-less homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,
Gene Name
DLX3
Protein name
Homeobox protein DLX-3
Abbreviation
Dlx-3
Other name
DLX3; Homeobox protein DLX-3
Fields
Human gene ID
1747
Human protein sequence Database
O60479
Mouse gene ID
13393
Mouse protein sequence database
Q64205
Rat gene ID
Rat protein sequence database
Cellular localization
Nucleus .
Tissue expression
Eye,Foreskin,Placenta,
Storage
-20°C/1 year

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Dlx-3 Polyclonal Antibody

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