Espn (espin)

基因基本信息

Espn 基因表型（MGI）

Homozygotes for a spontaneous mutation exhibit short and thin cochlear hair cell stereocilia, progressive degeneration of cochlear and vestibular hair cells, severe deafness, vestibular dysfunction, and poor mothering ability. Homozygotes lacking the long isoform show loss of staircase organization in extrastriolar vestibular hair bundles and thin vestibular stereocilia but no vestibular or hearing deficits.

获取 Espn 基因编辑小鼠

鼠来宝提供 Espn 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+。