Ercc1 (excision repair cross-complementing rodent repair deficiency, complementation group 1)

基因基本信息

Ercc1 基因表型（MGI）

Nullizygous mutations result in growth and liver failure, nuclear anomalies and postnatal death, and may lead to spleen hypoplasia, altered isotype switching, B cell hypoproliferation, dystonia, ataxia, renal failure, sarcopenia, kyphosis, early replicative aging and sensitivity to oxidative stress.

获取 Ercc1 基因编辑小鼠

鼠来宝提供 Ercc1 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+。