Maurer J, Thiel E
Department of Hematology and Oncology, Universitätsklinikum Steglitz, Free University of Berlin, Federal Republic of Germany.
Blut. 1990 Dec;61(6):350-3. doi: 10.1007/BF01738548.
We have developed a rapid method for the detection of bcr/abl mRNAs, the products of the BCR/ABL fusion genes. The method is based on the polymerase-chain-reaction (PCR). Through the use of additional internal primers it is possible to detect directly a single Ph1-positive cell among 10(5) unaffected cells thus omitting time-consuming blotting procedures. The whole analytical procedure starting from RNA isolation to agarose gel electrophoresis including two rounds of PCR can be performed in less than six hours.
我们已经开发出一种快速检测bcr/abl信使核糖核酸(mRNA)的方法,该mRNA是BCR/ABL融合基因的产物。此方法基于聚合酶链反应(PCR)。通过使用额外的内部引物,能够直接在10⁵个未受影响的细胞中检测出单个Ph1阳性细胞,从而省去了耗时的印迹程序。从RNA分离到琼脂糖凝胶电泳,包括两轮PCR的整个分析过程可在不到6小时内完成。