融合
DNA
计算生物学
限制性酶
DNA测序
遗传学
克隆(编程)
生物
计算机科学
语言学
哲学
程序设计语言
作者
Kamonchai Cha‐aim,Hisashi Hoshida,Tomoaki Fukunaga,Rinji Akada
标识
DOI:10.1007/978-1-61779-564-0_8
摘要
Overlap extension or fusion PCR is thought to be a simple and easy method to produce fusion DNA fragments without the need for restriction enzyme digestion and DNA ligation. However, this method has not been used frequently, probably as it is not always reliable. When natural sequences are used for overlap sequences, sometimes either no fusion DNA is produced or only faint DNA bands are detected owing to low annealing between the overlap sequences selected. Here, we introduce several artificial overlap sequences, most of which are GC-rich, that can be used for reliable fusion PCR. We describe how these overlap sequences can be used for fusion DNA construction, in-frame gene fusion, and cloning in yeast.
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