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1)  multiplex PCR assay
多重PCR鉴定
1.
coli O26:H11 was isolated from a patient with diarrhea by means of slide method of seroagglutination, biochemical reactions by biomerienx-VITEK32 AMS with GN1+ card, multiplex PCR assay, cytotoxicity test on Vero cells, ESBL assay and the susceptibility tests to 21 antibiotics, and was identified by the NCCLS standard.
coliO26∶H11进行多重PCR鉴定、Vero细胞毒性试验、ESBL试验和21种抗生素的药敏试验,并结合NCCLS标准进行判定。
2)  Triplex PCR identification
三重PCR鉴定
3)  PCR identification
PCR鉴定
1.
PCR identification of the pathogens causing black leaf spot of cruciferae vegetables;
十字花科蔬菜黑斑病菌的PCR鉴定
4)  PCR analysis
PCR鉴定
1.
These recombinant plasmids pET-BA and pBI-Bt-BA were confirmed by restriction enzyme and PCR analysis and the results showed that these recombinant plasmids were constructed successfull.
把双价基因(Bt-BA)连接到原核表达载体pET28a和植物表达载体pBI121上,经过限制性酶切分析和PCR鉴定,结果表明:含有双价基因的原核和真核重组表达质粒均已构建成功。
2.
These recombinant plasmids pET-NAMP-Bt and pBI-NAMP-Bt were confirmed by restriction enzyme and PCR analysis and the results showed that these recombinant plasmids were constructed successfully.
把融合基因(NAMP-Bt)连接到原核表达载体pET-28a和植物表达载体pBI-121上,经过限制性酶切分析和PCR鉴定,结果表明含有融合基因的原核和真核重组表达质粒均已构建成功,并将该融合基因转入烟草,已获得抗性小植株。
3.
These recombinant plasmids pBI101-BmKITS-chi and pWM101-chi-BmKITS were confirmed by restriction enzyme and PCR analysis and the results showed that these recombinant plasmids were constructed successfully.
将蝎毒基因BmKITS和几丁质酶基因chitinase2个抗虫基因采用不同的启动子ubi或35S,连到2个高效的植物表达载体pWM101和pBI101中,2个重组表达质粒分别经过限制性酶切分析和PCR鉴定,实验结果表明2个含有双价抗虫基因的植物重组表达质粒均已构建成功。
5)  PCR-16S rDNA identification
PCR-16SrDNA鉴定
6)  PCR-Southern analysis
PCR-Southern鉴定
补充资料:人民法院补充鉴定和重新鉴定有疑问证据的职权
人民法院补充鉴定和重新鉴定有疑问证据的职权:对鉴定结论有疑问的,人民法院可以指派或者聘请有专门知识的人或者鉴定机构,对案件中的某些专门性问题进行补充鉴定或者重新鉴定。――――《最高人民法院关于执行〈中华人民共和国刑事诉讼法〉若干问题的解释》第59条
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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