Jackson V N, Price N T, Halestrap A P
Department of Biochemistry, University of Bristol, UK.
Biochim Biophys Acta. 1995 Sep 13;1238(2):193-6. doi: 10.1016/0005-2736(95)00160-5.
PCR was used to amplify the coding region of CHO MCT1 cDNA. This was then used to screen a rat skeletal muscle cDNA library which lead to the isolation of a full length cDNA encoding MCT1 from rat. The cDNA derived amino acid sequence shows 94% and 86% identity to CHO and human MCT1, respectively.
采用聚合酶链反应(PCR)扩增中国仓鼠卵巢细胞(CHO)单羧酸转运蛋白1(MCT1)的编码区。然后用其筛选大鼠骨骼肌cDNA文库,从而分离出大鼠MCT1的全长cDNA。该cDNA推导的氨基酸序列与CHO及人MCT1的一致性分别为94%和86%。