摘要
分析了PCR过程中带有错误碱基拷贝的量变过程,得出不同循环(n)后不同类型拷贝数的计算通式并以逐次代入方式归纳出PCR产物中无错误碱基拷贝最低比率(R)和有效循环数(N),拷贝酶促合成链长(H)及错配率(f)的关系式R_n=(1-Hf/2) ̄(N-1)(1-Hf),对PCR技术制备表达用DNA片段有指导意义.
The quantity change of the copieswith mismatch bases in PCR products wasanalyzed.The general formulas of numbers ofcopies in different modes after certain cycles(n)were gained and the math relation betweenthe minimum(R_n)of the non-base-mismatchcopy proportion of PCR products and the effi-ciency cycle numbers(N),the copy chainlength(H)catalyzed by Taq polymerase andthe mismatch frequency(f)was concluded byway of substituting step by step:R_n=(1-Hf/2) ̄(N-1)(1-Hf).The formula has a guid-ance sense for preparing the gene segmentsused for the gene expression by PCR tech-nique.
出处
《生物化学与生物物理进展》
SCIE
CAS
CSCD
北大核心
1995年第3期275-277,287,共4页
Progress In Biochemistry and Biophysics
关键词
碱基错配
基因表达
聚合酶链反应
polymerase chain reaction,basemismatch,gene expression