Total Dlx-3 Cell-Based Colorimetric ELISA Kit
- 货号：KA3473C
- 应用：ELISA
- 种属：Human;Mouse
- 其他名称：
- Homeobox protein DLX-3
- 背景：
- 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.,
- 功能：
- blood vessel development, placenta development, vasculature development, regulation of transcription, DNA-dependent, regulation of transcription, regulation of RNA metabolic process,
