Wood W I, Gitschier J, Lasky L A, Lawn R M
Proc Natl Acad Sci U S A. 1985 Mar;82(6):1585-8. doi: 10.1073/pnas.82.6.1585.
An oligonucleotide hybridization procedure has been developed that eliminates the preferential melting of A X T versus G X C base pairs, allowing the stringency of the hybridization to be controlled as a function of probe length only. This technique, which uses tetramethylammonium chloride, is especially helpful whenever a highly complex library is screened with a pool of oligonucleotide probes, which usually vary widely in base composition. The procedure can also be applied advantageously whenever an exact match to an oligonucleotide probe is desired, such as in screening for clones having as little as a single-base alteration generated by in vitro mutagenesis.
已开发出一种寡核苷酸杂交程序,该程序消除了A×T碱基对与G×C碱基对的优先解链现象,使得杂交的严谨性仅作为探针长度的函数来控制。这种使用四甲基氯化铵的技术,在使用寡核苷酸探针池筛选高度复杂文库时特别有用,因为这些探针的碱基组成通常差异很大。当需要与寡核苷酸探针精确匹配时,例如筛选由体外诱变产生的仅有单碱基改变的克隆时,该程序也可有利地应用。