互补DNA
生物
分子生物学
羊毛甾醇
cDNA末端的快速扩增
克隆(编程)
分子克隆
核酸序列
寡核苷酸
ATP合酶
基因
遗传学
生物化学
甾醇
程序设计语言
胆固醇
计算机科学
作者
ChungKi SUNG,Masaaki Shibuya,Ushio Sankawa,Yutaka EBIZUKA
摘要
A cDNA encoding human lanosterol synthase, the enzyme responsible for the backbone formation step in sterol biosynthesis, was cloned by extensive application of PCRs. Five degenerate oligonucleotide primers (139S, 440S, 528A, 575A and 712A) corresponding to the homologous amino acid sequences among the known 2, 3-oxidosqualene cyclase (OSC) were designed. PCR with one pair (440S and 528A) of five primers yielded a 285-bp fragment. PCRs with the primers based on the obtained fragment and the degenerate primers (139S and 712A) gave longer fragments. Finally, full nucleotide sequence of cDNA was obtained by a "rapid amplification of cDNA ends"(RACE) method.
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