Trayhurn P, Duncan J S, Nestor A, Thomas M E, Eastmond N C, Rayner D V
Division of Biochemical Sciences, Rowett Research Institute, Bucksburn, Aberdeen, UK.
Electrophoresis. 1995 Mar;16(3):341-4. doi: 10.1002/elps.1150160157.
A simplified, nonradioactive procedure for the detection of specific mRNAs on Northern blots has been developed, utilizing digoxigenin-labelled oligonucleotides and chemiluminescence. Antisense oligonucleotide (30-35 mer) probes were designed and synthesised based on published cDNA and gene sequences. These probes were end-labelled (5') with digoxigenin. Total RNA was fractionated by agarose gel electrophoresis and capillary blotted onto positively charged nylon membranes. After hybridization, the mRNA/digoxigenin-labelled oligonucleotide complex was detected by a chemiluminescence-based method using disodium 3-(4-methoxyspiro-[1,2-dioxetane-3-2'(5'chloro)- tricyclo[3.3.1.13.7]decane]-4-yl)phenyl phosphate (CSPD) as substrate. The advantages of this simplified technique for detecting mRNAs in physiological and nutritional studies are described.
已开发出一种用于在Northern印迹上检测特定mRNA的简化非放射性程序,该程序利用地高辛标记的寡核苷酸和化学发光法。基于已发表的cDNA和基因序列设计并合成了反义寡核苷酸(30 - 35聚体)探针。这些探针用地高辛进行5'末端标记。总RNA通过琼脂糖凝胶电泳进行分级分离,然后通过毛细作用印迹到带正电荷的尼龙膜上。杂交后,使用3-(4-甲氧基螺[1,2 - 二氧杂环丁烷 - 3 - 2'(5'-氯)-三环[3.3.1.13.7]癸烷]-4 - 基)苯基磷酸二钠(CSPD)作为底物,通过基于化学发光的方法检测mRNA/地高辛标记的寡核苷酸复合物。描述了这种简化技术在生理和营养研究中检测mRNA的优势。