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人 NTRK3 抗体对
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人 NTRK3 抗体对

01AB01259

Neurotrophic receptor tyrosine kinase 3 (NTRK3), also known as TrkC, is a membrane-bound receptor tyrosine kinase that specifically binds neurotrophin-3 (NT-3) with high affinity. Structurally, NTRK3 consists of an extracellular ligand-binding domain, a single transmembrane helix, and an intracellular tyrosine kinase domain. Upon NT-3 binding, NTRK3 dimerizes and autophosphorylates, activating downstream signaling pathways such as PI3K/AKT, MAPK, and PLCγ, which regulate neuronal survival, differentiation, proliferation, and synaptogenesis. Multiple isoforms of NTRK3 exist due to alternative splicing, with some lacking kinase activity but still influencing neuronal differentiation. NTRK3 also functions as a dependence receptor, promoting apoptosis in the absence of ligand. Clinically, NTRK3 is implicated in various cancers including medulloblastoma, secretory breast carcinoma, and upper tract urothelial carcinomas, often through gene fusions or altered expression. Its promoter methylation status serves as a biomarker in colorectal and esophageal cancers.

Human
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技术参数

靶点基因名
NTRK3
基因别名
TRKC
蛋白别名
neurotrophic receptor tyrosine kinase 3; NTRK3
UniProt
Q16288
物种
Human

产品详情

靶点名称
NTRK3
蛋白名称
neurotrophic receptor tyrosine kinase 3
蛋白别名
NT-3 growth factor receptor; GP145-TrkC; Trk-C; Neurotrophic tyrosine kinase receptor type 3; TrkC tyrosine kinase
靶点基因名
NTRK3
基因别名
TRKC
UniProt
Q16288
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Neurotrophic receptor tyrosine kinase 3 (NTRK3), also known as TrkC, is a membrane-bound receptor tyrosine kinase that specifically binds neurotrophin-3 (NT-3) with high affinity. Structurally, NTRK3 consists of an extracellular ligand-binding domain, a single transmembrane helix, and an intracellular tyrosine kinase domain. Upon NT-3 binding, NTRK3 dimerizes and autophosphorylates, activating downstream signaling pathways such as PI3K/AKT, MAPK, and PLCγ, which regulate neuronal survival, differentiation, proliferation, and synaptogenesis. Multiple isoforms of NTRK3 exist due to alternative splicing, with some lacking kinase activity but still influencing neuronal differentiation. NTRK3 also functions as a dependence receptor, promoting apoptosis in the absence of ligand. Clinically, NTRK3 is implicated in various cancers including medulloblastoma, secretory breast carcinoma, and upper tract urothelial carcinomas, often through gene fusions or altered expression. Its promoter methylation status serves as a biomarker in colorectal and esophageal cancers.