方法组织化学、原位杂交和完整细胞RNA斑点印迹。

Methods Histochemistry, in situ hybridization and intact cell RNA dot blot techniques were used.

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经体外蛋白质—蛋白质之间的相互作用和蛋白质印迹杂交方法进一步验证了PBP1和BNP23的相互作用；

In vitro the interaction between BNP23 and PBP1 was ascertained by means of the protein-protein interaction and western blotting.

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免疫印迹杂交结果显示MYOG和MYOD的蛋白质表达水平也发生了与基因表达相一致的变化。

The results of Western blotting showed that protein expression levels of MYOG and MYOD also changed as same as the gene expression levels.

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