目的确定提高柱式胶回收试剂盒d NA回收效率的最佳条件。
AIM To determine the optimal conditions for high DNA extraction efficiency from gels with gel extraction kit.
按照DNA凝胶回收试剂盒的操作说明，回收纯化P CR产物。
According to the instructions of DNA gel extraction kit, recover purified PCR product.
对扩增产物进行电泳鉴定，最后将PCR产物经胶回收试剂盒纯化，以备酶切。
Electrophoresis of the PCR products was identified, and finally PCR product was purified by gel extraction kit to prepare for digestion.
方法：以三种栽培的食用菌为材料，采用CTAB结合DNA凝胶回收试剂盒进行基因组DNA的分离和纯化。
Method: The genomic DNA was extracted by combined method of CTAB and DNA gel purification kit from sporophore of three cultivated edible fungus.
含2 %PVP的1 %琼脂糖凝胶电泳纯化，用DNA凝胶回收试剂盒回收后没有得到纯化后的土壤微生物总DNA。
Soil microbial total DNA could not be obtained through DNA gel extraction kit after purification with 1% Sepharose containing 2% of PVP (polyvinylpyrrolidone) agarose gel electrophoresis.
仫佬族、壮族、汉族各随机选取一份PCR产物以切胶回收P CR产物纯化试剂盒纯化。
Then, one random portion of PCR products from Mulao, Zhuang and Han was purified with DNA Purification Kit.
仫佬族、壮族、汉族各随机选取一份PCR产物以切胶回收P CR产物纯化试剂盒纯化。
Then, one random portion of PCR products from Mulao, Zhuang and Han was purified with DNA Purification Kit.
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