Bcat2 (branched chain aminotransferase 2, mitochondrial)

基因基本信息

Bcat2 基因表型（MGI）

The metabolism of branched chain amino acid is impaired in homozygous null mice, resulting in a phenotype similar to human maple syrup urine disease. Mutants exhibit a failure to thrive and die prematurely, though the severity of the symptoms can be ameliorated with a restricted diet.

获取 Bcat2 基因编辑小鼠

鼠来宝提供 Bcat2 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+。