Tsongalis G J, Silverman L M
Department of Hospital Laboratories and Pathology, University of North Carolina, Chapel Hill 27514.
Ann Clin Lab Sci. 1994 Sep-Oct;24(5):436-40.
Using the polymerase chain reaction (PCR) specific gene target sequences can be routinely amplified from isolated nucleic acids. However, this does not allow the investigator the option of correlating the presence of amplified product with cellular localization. When PCR is performed in situ and coupled with either a direct or indirect method of detecting amplified product, a powerful investigative tool exists. Owing to variability in results, the features of in situ PCR which are most likely to contribute to these effects are described. Also described is an amplification chamber for localized in situ amplification (LISA) which utilizes tissue culture cloning rings and allows for the amplification of gene target sequences in specific regions of paraffin-embedded tissue sections.
使用聚合酶链反应(PCR)可从分离出的核酸中常规扩增特定基因靶序列。然而,这并不允许研究人员将扩增产物的存在与细胞定位相关联。当原位进行PCR并结合直接或间接检测扩增产物的方法时,就形成了一种强大的研究工具。由于结果存在变异性,本文描述了原位PCR最可能导致这些影响的特征。还描述了一种用于局部原位扩增(LISA)的扩增室,它利用组织培养克隆环,能够在石蜡包埋组织切片的特定区域扩增基因靶序列。