Shivers B D, Harlan R E, Pfaff D W, Schachter B S
J Histochem Cytochem. 1986 Jan;34(1):39-43. doi: 10.1177/34.1.3510246.
A procedure is described for combining avidin-biotinylated horseradish peroxidase immunocytochemistry, for localizing peptides or proteins, with in situ hybridization for localizing mRNA autoradiographically in the same cryostat section of paraformaldehyde-fixed rat pituitary. Protection against enzymatic degradation of target mRNAs during the immunocytochemical step was necessary and was accomplished by including an RNase inhibitor, 0.04% diethylpyrocarbonate, in primary and secondary antisera. This combination of methods may be useful in other tissues, as well, for (a) determining the relation of protein content to the concentration of its encoding mRNA, (b) proving the synthetic capacity of a cell in which a protein has been localized, (c) determining immunological or nucleic acid probe specificity, or (d) as an alternative to double-labeling immunocytochemical methods.
本文描述了一种方法,可将用于定位肽或蛋白质的抗生物素蛋白-生物素化辣根过氧化物酶免疫细胞化学,与用于在多聚甲醛固定的大鼠垂体的同一低温恒温器切片中通过放射自显影定位mRNA的原位杂交相结合。在免疫细胞化学步骤中防止靶mRNA的酶促降解是必要的,这通过在一抗和二抗中加入一种核糖核酸酶抑制剂0.04%焦碳酸二乙酯来实现。这种方法组合在其他组织中也可能有用,用于:(a)确定蛋白质含量与其编码mRNA浓度之间的关系;(b)证明已定位蛋白质的细胞的合成能力;(c)确定免疫或核酸探针的特异性;或(d)作为双标记免疫细胞化学方法的替代方法。