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TRPS1 is a member of the GATA-like family of zinc finger transcription factors.1 It is composed of seven zinc-finger domains, a cysteine-rich region, a GATA-like zinc-finger domain, and two Ikaros-like zinc-finger domains. TRPS1 is ubiquitously expressed and found in the nucleus where it binds GATA-binding sequences and functions as a transcriptional repressor.1,2 It is involved in organ development, cell cycle regulation and progression, and the regulation of bone and tooth mineralization.3,4,2 Deletion or loss-of-function mutations in TRPS1 are associated with Langer-Giedion syndrome, also known as trichorhinophalangeal syndrome type 1, a condition characterized by learning disabilities, craniofacial abnormalities, ectodermal dysplasia, hip malformations, and decreased stature.5 Cayman's TRPS1 Rabbit Monoclonal Antibody (Clone RM518) can be used for immunohistochemistry (IHC) and Western blot (WB) applications.
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1. Structure and function of GC79/TRPS1, a novel androgen-
2. Functional mechanisms of TRPS1 in disease progression and its potential role in personalized medicine. Pathol. Res. Pract. 237, 154022 (2022).
3. Dual role of the Trps1 transcription factor in dentin mineralization. The Journal of Biological Chemisty (2014).
4. A central role for TRPS1 in the control of cell cycle and cancer development. Oncotarget 5(17), 7677-7690 (2014).
5. Mutations in a new gene, encoding a zinc-