Murphy D
Neuropeptide Laboratory, Institute of Molecular and Cell Biology, National University of Singapore, Republic of Singapore.
Methods Mol Biol. 1993;18:449-51. doi: 10.1385/0-89603-245-0:449.
This chapter describes a standard method for the hybridization of labeled DNA probes to nucleic acids bound to a nylon matrix. Filters bearing bound nucleic acids produced by Northern blotting of RNA (Chapter 39), Southern blotting of DNA (Chapter 37), and slot blotting of DNA (Chapters 35) or RNA (Chapter 40) are hybridized to labeled probes using the method described below. The advantages of this method are, first, that the use of a high concentration of SDS in the hybridization buffer ensures a low background level of nonspecific probe adherence to the membrane and, second, an extended period of filter prehybridization is not required. The inclusion of a large amount of SDS does, however, necessitate that the nucleic acids are covalently bonded to the matrix by UV light crosslinking. The inclusion of formamide (15% [v/v]) is also recommended in order to reduce the viscosity of the hybridization buffer. Formamide also has the effect of reducing the temperature of the hybridization reaction.
本章介绍了一种将标记的DNA探针与结合在尼龙基质上的核酸进行杂交的标准方法。通过RNA的Northern印迹法(第39章)、DNA的Southern印迹法(第37章)以及DNA(第35章)或RNA(第40章)的狭缝印迹法产生的带有结合核酸的滤膜,使用下述方法与标记探针进行杂交。该方法的优点在于,其一,杂交缓冲液中使用高浓度的SDS可确保非特异性探针附着于膜上的背景水平较低;其二,无需延长滤膜预杂交时间。然而,大量SDS的存在确实要求核酸通过紫外线交联共价结合到基质上。为降低杂交缓冲液的粘度,还建议加入甲酰胺(15%[v/v])。甲酰胺还具有降低杂交反应温度的作用。