Overview

Properties

Applications

Our Abpromise guarantee covers the use of ab64056 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
ELISA Use at an assay dependent dilution.
WB 1/40. Predicted molecular weight: 32 kDa.
IHC-P 1/100.

Target

  • FunctionLikely to play a regulatory role in the development of the ventral forebrain. May play a role in craniofacial patterning and morphogenesis.
  • Involvement in diseaseDefects 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.
    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.
  • Sequence similaritiesBelongs to the distal-less homeobox family.
    Contains 1 homeobox DNA-binding domain.
  • Cellular localizationNucleus.
  • Information by UniProt
  • Database links
  • Alternative names
    • AI4 antibody
    • Distal less homeo box 3 antibody
    • DLX 3 antibody
    • Dlx3 antibody
    • DLX3 distalless homeobox 3 antibody
    • DLX3_HUMAN antibody
    • Homeobox protein DLX 3 antibody
    • Homeobox protein DLX-3 antibody
    • Homeobox protein Dlx3 antibody
    • TDO antibody
    see all

References for Anti-DLX3 antibody (ab64056)

ab64056 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"