Total Dlx-3 Cell-Based Colorimetric ELISA Kit

  • Catalog No.：KA3473C
  • Applications：ELISA
  • Reactivity：Human;Mouse
    • Gene Name：
    • DLX3
    • Human Gene Id：
    • 1747
    • Human Swiss Prot No：
    • O60479
    • Mouse Swiss Prot No：
    • Q64205
    • Storage Stability：
    • 2-8°C/6 months
    • Other Name：
    • Homeobox protein DLX-3
    • Detection Method：
    • Colorimetric
    • Background：
    • 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.,
    • Function：
    • blood vessel development, placenta development, vasculature development, regulation of transcription, DNA-dependent, regulation of transcription, regulation of RNA metabolic process,
    • Subcellular Location：
    • Nucleus .

    Attributes

    • Code：
    • KA3473C
    • Size
    • 96 / well
    • Price$：
    • 330
    • Delivery：
    • 2024-08-02
    Order

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