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抗人 TRPS1 抗体对
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抗人 TRPS1 抗体对

01AB01392

Transcriptional repressor GATA binding 1 (TRPS1) is a zinc finger transcription factor that specifically binds to GATA sequences and represses the expression of GATA-regulated genes at selected sites and stages in vertebrate development. The protein contains nine zinc-finger domains, including a single GATA-type DNA binding domain flanked by two potential regulatory domains. TRPS1 functions downstream of BMP7 and GDF5 signaling pathways, regulating key developmental processes including chondrocyte condensation, proliferation, and maturation. It plays crucial roles in bone development, hair follicle morphogenesis, kidney tubule formation, and phalangeal joint development by targeting genes such as Sox9, Pthrp, Stat3, and Runx2, and by directly interacting with Gli3. TRPS1 is also implicated in tumorigenesis, invasion, and metastasis in prostate and breast cancers. Mutations in the TRPS1 gene are associated with tricho-rhino-phalangeal syndrome (TRPS) types I and III, which are autosomal dominant skeletal disorders characterized by craniofacial and skeletal abnormalities.

Human
规格起售价
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技术参数

靶点基因名
TRPS1
蛋白别名
transcriptional repressor GATA binding 1; TRPS1
UniProt
Q9UHF7
物种
Human

产品详情

靶点名称
TRPS1
蛋白名称
transcriptional repressor GATA binding 1
蛋白别名
Zinc finger transcription factor Trps1; Tricho-rhino-phalangeal syndrome type I protein; Zinc finger protein GC79
靶点基因名
TRPS1
UniProt
Q9UHF7
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Transcriptional repressor GATA binding 1 (TRPS1) is a zinc finger transcription factor that specifically binds to GATA sequences and represses the expression of GATA-regulated genes at selected sites and stages in vertebrate development. The protein contains nine zinc-finger domains, including a single GATA-type DNA binding domain flanked by two potential regulatory domains. TRPS1 functions downstream of BMP7 and GDF5 signaling pathways, regulating key developmental processes including chondrocyte condensation, proliferation, and maturation. It plays crucial roles in bone development, hair follicle morphogenesis, kidney tubule formation, and phalangeal joint development by targeting genes such as Sox9, Pthrp, Stat3, and Runx2, and by directly interacting with Gli3. TRPS1 is also implicated in tumorigenesis, invasion, and metastasis in prostate and breast cancers. Mutations in the TRPS1 gene are associated with tricho-rhino-phalangeal syndrome (TRPS) types I and III, which are autosomal dominant skeletal disorders characterized by craniofacial and skeletal abnormalities.