TBX15/18 Polyclonal Antibody, 100ul ssDNA Synthesis anhidrosis

anhidrosis

Mutations in this gene cause xeroderma pigmentosum complementation group E

This gene is testis-specific and contains a polymorphic region| resulting in isoforms with varying numbers of C-terminal repeats

Mutations in CUBN may play a role in autosomal recessive megaloblastic anemia

This gene encodes a member of the Ser/Thr protein kinase family and the TGFB receptor subfamily

TBX15/18 Polyclonal Antibody, 100ul ssDNA Synthesis anhidrosisTBX18 codes for a member of an evolutionarily conserved family of transcription factors that plays a crucial role in embryonic development. The family is characterized by the presence of the DNA binding T box domain and is divided into five sub families based on sequence conservation in this domain. The T box transcription factor TBX18 belongs to the vertebrate specific Tbx1 sub family. The protein acts as a transcriptional repressor by antagonizing