Kcnj11 (potassium inwardly rectifying channel, subfamily J, member 11)

基因基本信息

Kcnj11 基因表型（MGI）

Homozygotes for a targeted null mutation exhibit impaired insulin secretion, mild glucose intolerance, reduced glucagon secretion in response to hypoglycemia, hypoxia-induced seizure susceptibility, and stress-induced arrhythmia and sudden death.

获取 Kcnj11 基因编辑小鼠

鼠来宝提供 Kcnj11 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+。