According to the instructions of DNA gel extraction kit, recover purified PCR product.
按照DNA凝胶回收试剂盒的操作说明，回收纯化P CR产物。
AIM To determine the optimal conditions for high DNA extraction efficiency from gels with gel extraction kit.
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。
Genomic DNA of mature leaf in pueraria DC is extracted in SDS method. And the DNA is purified with DNA gel Extraction kit.
采用SDS裂解法提取了葛属植物成熟叶片的基因组dna，并利用凝胶纯化试剂盒进行了纯化。
Electrophoresis of the PCR products was identified, and finally PCR product was purified by gel extraction kit to prepare for digestion.
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。
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.
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.
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。
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