Ntrk1 (neurotrophic tyrosine kinase, receptor, type 1)

基因基本信息

Ntrk1 基因表型（MGI）

Homozygous null mutations result in premature death due to severe sensory and sympathetic neuropathies. A conditional mutant mouse exhibits defects in mast cell and B cell physiology. Homozygotes for a point mutation are normal, but are subject to pharmacological control of signalling. Homozygosity for the p.R685A mutation affects sympathetic neuron development.

获取 Ntrk1 基因编辑小鼠

鼠来宝提供 Ntrk1 相关基因敲除、条件敲除、人源化、点突变小鼠定制，以及配套动物实验、代养净化、检测研发服务。双繁育基地（鄂州葛店·广东佛山），标准化笼位 10 万+。