RAPD were selected in this study used 80 random primers, 27 primer pairs of DNA can be amplified and can be found resistance genes and gene perceptual difference.
共筛选80个RAPD随机引物，其中有27个引物能对DNA扩增并能发现其中抗性基因与感性基因的区别。
Objective To study the effect of modified improved primer extension preamplification (IPEP) on STR analysis of trace DNA.
目的探讨改良扩增前引物延伸(ipep)法对痕量DNA样本s TR检测分型的效果。
Single primer PCR was a method of chromosome walking to isolate sequences flanking a known DNA sequence with only one primer.
单引物pcr是一种只用一条引物就可以克隆已知序列侧翼未知区域的染色体步移方法。
According to the bacteria gene sequence, we also designed PCR primer, and collected genome DNA for PCR rapid test, then tested and contrasted sequence.
根据菌属基因序列设计PCR引物，提取基因组dna进行PCR快速检测，然后进行测序比对。
Control DNA samples that genotypes known were used to confirm the sensitivity and specificity of each sequence-specific primer.
引物的特异性和灵敏度采用基因型已知的质控DNA进行验证。
SeqState - primer design and sequence statistics for phylogenetic DNA data sets.
进化DNA数据的引物设计序列统计软件。
The primer extension experiment showed the aggregation of DNA template by photooxydation.
引物延伸反应表明DNA分子发生聚合。
The method of isolating genomic DNA and RAPD primer screening of were studied. The results are as follows;
以毛豹皮樟叶片为材料，对其DNA提取方法和RAPD引物的筛选进行了研究。
The effect of different extraction buffers, different temperatures and different treatment times on the quality of DNA were compared by examining the DNA with random-primer PCR.
用随机引物pcr检测模板dna的质量，比较了不同提取缓冲液、不同温度及不同处理时间对模板dna质量的影响。
The products amplified by single-primed PCR formed DNA fingerprints with the specificity of primer-template.
由此进行单引物PCR扩增，它们的扩增产物形成了稳定的引物——模板特异的DNA指纹图谱。
The products amplified by single-primed PCR formed DNA fingerprints with the specificity of primer-template.
由此进行单引物PCR扩增，它们的扩增产物形成了稳定的引物——模板特异的DNA指纹图谱。
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