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Please note that all translations are automatically generated. Click here for the English version.
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02:08 min
January 12th, 2024
DOI :
10.3791/200816-v
Transcript
要进行DNA提取,首先向从眼液中获得的细胞沉淀中加入适量的细胞裂解液。上下移液,使溶液充分混合。细胞完全裂解后,加入蛋白质沉淀溶液,占总体积的三分之一。
现在,涡旋并剧烈混合 20 到 30 秒。然后在室温下以 3000g 旋转三分钟。同时,将 300 微升异丙醇转移到干净的微量离心管中。
离心完成后,小心地将上清液移液到含有异丙醇的试管中。接下来,向试管中加入 1.5 微升糖原并倒置试管以充分混合。将试管置于零下 20 摄氏度的冰箱中一小时或过夜,以促进 DNA
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