Results: The three primers can effectively identify the genuineness of Bupleurum chinense.

结果: 3种引物能有效地鉴别北柴胡样品的道地性.

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Seven sets of primers were designed toamplify the ERG 11 gene.

设计7对引物,分段扩增白念珠菌酵母相和菌丝相细胞的ERG11基因.

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There were 89 SSR sequences used for design of special primers.

加上搜索数据库所获得的1个SSR序列,一共89个序列用于特异引物的设计.

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Methods: The erm genes of MRCNS were detected by degenerate primers amplification.

方法 　 应用兼并引物扩增MRCNS菌的erm基因.

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Just mix your template with a buffer and some primers.

只要模板,缓冲液加引物.

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Primer OPM - 15 was used to identify Races 1 and 4.

引物OPM-15能用来鉴定1号和4号生理小种.

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RT PCR was performed for APN gene expression in liver tissue.

(2)APN表达:根据兔APN基因 cDNA序列 设计引物,提取肝总RNA,利用RTPCR 方法,检测肝APNmRNA水平的变化.

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The particular random primer BA 1072 was selected from 110 primers.

所用RAPD引 物是从110个RAPD随机引物中筛选出的BA1072号引物.

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SeqState - primer design and sequence statistics phylogenetic DNA data sets.

进化DNA数据的引物设计序列统计软件.

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Totally 78 polymorphic DNA loci were amplified by 10 RAP D primers.

实验筛选出的10个RAPD引物共扩增出78条DNA多态片段.

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We demonstrated that rBCG - B 7 - 2 ( IgC + IgV ) possesses enhanced immunogenicity.

菌体洗涤后煮沸10分钟作为模板.以根据 hB7 一2 ( IgC+IgV ) 序列和pYL质粒MCS两端 序列设计的二对引物PCR后 切胶回收测序.

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Oligo ( dT ) 18 primer were from Sangon, Shanghai.

Oligo ( dT ) 18引物购自上海生工.

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Objective : To compare the affection of different primers to detect Mycoplasma pneumonia ( Mp ).

目的: 比较不同引物对 肺炎 支原体检测的影响.

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Objective : To establish DNA typing for HLA - DR 4 antigen by chain reaction with sequence - specific primers ( PCR - SSP ).

目的: 采用顺序特异引物聚合酶链反应(PCR-SSP ) 建立人类白细胞抗原DR4位点的DNA分型方法.

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We can't use these designed primers as primers designed on the mutated - type site of Pinb - D 1 b .

这几种突变体的筛选上,不能像Pinb -D1b 突变体一样根据突变位点设计引物使用.

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