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文献和实验of GSK-3expression by RNA interference using small interfering RNAs(siRNAs) or short hairpin RNA (shRNA) targeting vectors specificfor each isoform (Fig. 5.1b ) (25) . Although the inhibition of GSK-3 kinase activity by a certaininhibitor
upon the dual pulldown to incorporate a third pulldown which is an iteration of the ChIP and is a pulldown for H3K27me3+ (Figure 1b). The third assay described here is the biotin-RNA pulldown of a low-copy RNA that spans the siRNA targeted promoter region
0.5cm处铺上2cm宽的4层滤纸,待滤纸完全浸湿后,轻轻揭掉;贴上塑料加样板,每孔加透析完毕的样本IOuL,留二孔分别加血红蛋白和C4分型标准品,静置30min,待样本完全浸入琼脂糖凝胶中,揭掉加样板。将加样完毕的凝胶板放在冷却循环电泳槽上,样本放在阴极,打开冷却循环泵(10℃),接通电源控制电流在65~80mA,电泳45rain或待血红蛋白迁移到离加样孔6~7cm处,停止电泳。 (4)将抗C4血清1:2或1:4稀释,均匀铺在电泳完毕的琼脂糖凝胶上,37℃30~45min,然后放人生理盐水中漂洗
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