The framework of this work is to extract DNA from bacteria from the selected soil samples of Malaysia University, extract all six samples from the enzyme indexes with visual characteristics named in the sample collection place, namely S7a-1, S7a-11, F-14, F-1, F-110 and F-115, and use the 16s rRNA gene-specific primers (universal 16s rRNA primers) of these bacteria for PCR amplification.
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