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使用共价偶联到纤维素上的DNA进行核酸杂交。

Nucleic acid hybridization using DNA covalently coupled to cellulose.

作者信息

Noyes B E, Stark G R

出版信息

Cell. 1975 Jul;5(3):301-10. doi: 10.1016/0092-8674(75)90105-1.

Abstract

We describe a method for linking RNA and DNA covalently to finely divided cellulose through a diazotized aryl amine, which reacts primarily with guanine and uracil (thymine) residues of single strands. The high efficiency of coupling and high capacity of the cellulose for nucleic acid make possible a product with as much as 67 mug of nucleic acid per mg of cellulose. The product is especially suitable for hybridization experiments where very low backgrounds are important, and it is stable in 99% formamide at 80 degrees C so that hybridized nucleic acid can be recovered easily. Full length linear Simian Virus 40 (SV40) DNA, produced by cleavage of SV40(I) DNA with S1 nuclease, can be coupled to diazo cellulose with an efficiency of 80-90%, and is effective in hybridization experiments with SV40 DNA, complementary RNA synthesized in vitro from SV40(I) DNA with E. coli RNA polymerase, and the SV40-specific fraction of total RNA from SV40-infected and transformed cells. In these experiments an excess of cellulose-bound DNA was used, and the efficiency of hybridization was about 90% when ribonuclease treatment of the hybrids was omitted.

摘要

我们描述了一种通过重氮化芳基胺将RNA和DNA共价连接到细分纤维素上的方法,该重氮化芳基胺主要与单链的鸟嘌呤和尿嘧啶(胸腺嘧啶)残基反应。纤维素与核酸的高偶联效率和高容量使得每毫克纤维素能够结合多达67微克核酸的产品成为可能。该产品特别适用于背景极低至关重要的杂交实验,并且在80℃的99%甲酰胺中稳定,因此杂交后的核酸能够轻松回收。通过用S1核酸酶切割SV40(I)DNA产生的全长线性猿猴病毒40(SV40)DNA,可以以80 - 90%的效率与重氮纤维素偶联,并且在与SV40 DNA、用大肠杆菌RNA聚合酶从SV40(I)DNA体外合成的互补RNA以及来自SV40感染和转化细胞的总RNA中的SV40特异性部分进行的杂交实验中有效。在这些实验中使用了过量的纤维素结合DNA,并且当省略对杂交体的核糖核酸酶处理时,杂交效率约为90%。

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