Li J K, Johnson T M, Parker B D
Department of Biology, Utah State University, Logan 84322-5500.
Anal Biochem. 1988 Nov 1;174(2):471-6. doi: 10.1016/0003-2697(88)90045-0.
Individually wrapped, sterile disposable transfer pipets can be used in the isolation of ds-DNA and ds-RNA fragments from gels as well as in the screening of multiple samples in Southern, Northern, and Western blots without potential contamination by exogenous nucleases and proteases. The sensitivity and results obtained by this method are comparable to those obtained by conventional methods. All the prehybridization, blocking, hybridization, and detection processes can be performed within the transfer pipet. The isotopically labeled probes used in hybridization can easily be recovered, stored for reuse, or disposed of as waste with no potential contamination of personnel or laboratory equipment. Strip blots are stable in appropriate buffers within the liquepipets which can be shipped easily worldwide for comparative analyses by collaborative investigators. This method is simple, time saving, and inexpensive and is particularly suitable for multiple sample screening. Other potential applications of this procedure are discussed.
独立包装的无菌一次性移液器可用于从凝胶中分离双链 DNA 和双链 RNA 片段,以及在 Southern、Northern 和 Western 印迹中筛选多个样品,而不会受到外源性核酸酶和蛋白酶的潜在污染。通过这种方法获得的灵敏度和结果与传统方法相当。所有预杂交、封闭、杂交和检测过程都可以在移液器内进行。杂交中使用的同位素标记探针可以很容易地回收、储存以便重复使用或作为废物处理,不会对人员或实验室设备造成潜在污染。条带印迹在移液器内的适当缓冲液中很稳定,可以轻松运往世界各地供合作研究人员进行比较分析。这种方法简单、省时且成本低廉,特别适合多个样品的筛选。本文还讨论了该方法的其他潜在应用。