库氏按蚊(双翅目:库蚊科)复合体兄弟种A的简化非放射性DNA探针技术

B. D. Silva, G. Hapugoda, Eh Karuuanayake
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引用次数: 0

摘要

克隆了三个高度重复的DNA序列Rp36、Rp217和Rp234。利用生物素化标记和比色检测系统开发了culicifacies Giles, sensu lato作为非放射性DNA探针。这些非放射性的DNA探针区分了兄弟物种A与物种B和物种C。用稀释50倍的单个蚊子DNA提取物对culicifacies复合物进行点印迹杂交试验。生物素化的Rp217探针进一步通过一种更简单的方法进行检测,该方法包括对压扁的蚊头制备的印迹进行杂交。该技术避免了单独提取蚊子DNA,便于快速处理多个样本,同时还允许对一个蚊子样本进行多次现场分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A simplified non radioactive DNA probe technique for the field detection of sibling species A of the Anopheles culicifacies (Diptera: Culicidae) complex
Three cloned highly repetitive DNA sequences Rp36, Rp217 and Rp234 isolated from An. culicifacies Giles, sensu lato were developed as non radioactive DNA probes by using a biotinylated labeling and colorimetric detection system. These non radioactive DNA probes distinguish sibling species A from species B and C of the An. culicifacies complex in a dot blot hybridization assay using single mosquito DNA extracts diluted 50 fold. The biotinylated Rp217 probe was further assayed in a more simple procedure which involves the hybridization of blots prepared from squashed mosquito heads. This technique avoids the separate extraction of mosquito DNA and facilitates a number of samples to be processed rapidly while also allowing several field analyses to be carried out on one mosquito specimen.
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