Slc18a2 (solute carrier family 18 (vesicular monoamine), member 2)

基因基本信息

Slc18a2 基因表型（MGI）

Nullizygous mice exhibit early postnatal death accompanied by reduced body size, hypokinesia, and reduced brain monoamine levels. Hypomorphic mutants show impaired olfaction, gastroparesis, altered sleep latency, neuron degeneration, enhanced MPTP sensitivity, anxiety- and depressive-like behavior.

获取 Slc18a2 基因编辑小鼠

鼠来宝提供 Slc18a2 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+。