The positive bacteria strains were identified by random primer PCR.
随机引物pcr成功对阳性菌株进行了种属鉴定。
Methods: PCR with an anchoring primer in IS 1541 and random primer;
方法：用一条锚定的IS 1541内部锚定引物和一条随机引物进行PCR扩增；
METHODS Twenty one collected strains from ophthalmology ward were analyzed using random primer RAPD1 with RAPD.
方法用随机引物RAPD1，对眼科病房分离到的21株表皮葡萄球菌菌株DNA做RAPD并对其做药敏试验。
The thesis selected 4 effectives primer from 50 random primers produced by Shanghai Sangon Company in RAPD analysis.
RAPD分析中，应用了上海生工s系列的50个随机引物中筛选出的4个有效引物。
A TC-RT-PCR method basing on reverse transcription with random primer facilitated the detection for those samples mixed infected by ASGV and ACLSV.
用随机引物反转录，通过TC-RT-PCR检测ACLSV和ASGV复合感染的梨样品也均获得了目标片段。
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。
Second, through Parent C and parent F, 105 random primer were selected, and 87 primer acquired amplified products, 592 bands were gotten in all, 19 bands were polymorphism.
通过亲本C、F对105条随机引物进行筛选，共有87个引物获得了扩增产物，出现的谱带总数为592条。
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。
Objective to observe the impact of three fluorescence marker methods of primer marker, random inleakage marker and terminal transfer marker to Oligonucleotide microarray hybridize signal.
目的观察标记引物法、随机渗入标记法、末端转移标记法三种荧光标记法对寡核苷酸芯片杂交信号的影响。
Objective to observe the impact of three fluorescence marker methods of primer marker, random inleakage marker and terminal transfer marker to Oligonucleotide microarray hybridize signal.
目的观察标记引物法、随机渗入标记法、末端转移标记法三种荧光标记法对寡核苷酸芯片杂交信号的影响。
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