Kelly C D, Carter N D, de Boer P, Jeffery S, Moorman A F, Smith A
Department of Child Health, St George's Hospital Medical School, London, United Kingdom.
J Histochem Cytochem. 1991 Sep;39(9):1243-7. doi: 10.1177/39.9.1833447.
We carried out a variety of in situ methods of hybridization on rat liver and rat skeletal muscle using 35S-labeled or biotin-labeled rat carbonic anhydrase III (CAIII) cDNA clone. The methods were compared and evaluated. Use of the biotin system produced defined but nonspecific results which were shown not to be due to the biotinylated cDNA probe binding to the mRNA in the muscle sections. This artifact was shown to persist despite various attempts to eliminate it. Alternatively, using 35S-labeled cDNA gave reproducible results which were shown to be consistent with probe binding specifically to mRNA in the muscle section.
我们使用35S标记或生物素标记的大鼠碳酸酐酶III(CAIII)cDNA克隆,对大鼠肝脏和大鼠骨骼肌进行了多种原位杂交方法。对这些方法进行了比较和评估。生物素系统的使用产生了明确但非特异性的结果,结果表明这并非由于生物素化的cDNA探针与肌肉切片中的mRNA结合所致。尽管多次尝试消除这一假象,但它仍然存在。另外,使用35S标记的cDNA可得到可重复的结果,结果表明其与探针特异性结合肌肉切片中的mRNA一致。