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两种基因检测方法在病毒性心肌炎诊断中的应用 被引量:1
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作者 蒋文玲 罗宪玲 邝素娟 《心血管康复医学杂志》 CAS 2005年第2期118-120,共3页
目的:阐明基因检测手段在病毒性心肌炎(VMC)病原诊断中的作用。方法:采用RT-PCR、地高辛标记CBV3 -cDNA探针对PCR扩增产物进行斑点杂交,检测血标本中的柯萨奇病毒B组病毒(CBV)。结果:RT-PCR阳性检出率:心肌炎组为48.33%.对照组4.41%(P&l... 目的:阐明基因检测手段在病毒性心肌炎(VMC)病原诊断中的作用。方法:采用RT-PCR、地高辛标记CBV3 -cDNA探针对PCR扩增产物进行斑点杂交,检测血标本中的柯萨奇病毒B组病毒(CBV)。结果:RT-PCR阳性检出率:心肌炎组为48.33%.对照组4.41%(P<0.01)。斑点杂交阳性率:心肌炎组为51.67%,对照组4.41% (P<0.01)。检测CBV的两种方法阳性率无显著差异(P>0.05)。结论:两种方法特异性均高,敏感性无显著差异。 展开更多
关键词 病毒性心肌炎 柯萨奇B组病毒 聚合物酶链式反应 斑点杂交
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Bioleaching of Pb-Zn-Sn chalcopyrite concentrate in tank bioreactor and microbial community succession analysis 被引量:5
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作者 王军 赵红波 +3 位作者 庄田 覃文庆 朱珊 邱冠周 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2013年第12期3758-3762,共5页
The variation of microbial community structure was investigated for the tank bioleaching process of Pb-Zn-Sn chalcopyrite concentrate in the presence of mixed moderately thermophilic bacteria. The parameters, such as ... The variation of microbial community structure was investigated for the tank bioleaching process of Pb-Zn-Sn chalcopyrite concentrate in the presence of mixed moderately thermophilic bacteria. The parameters, such as pH value, solution potential and concentrations of metal ions, were determined by the method of polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to analyze the succession of microbial community. The results showed that a final copper extraction rate of 85.6% could be obtained after tank bioleaching for 30 d. The Acidithiobacillus caldus was the dominant population with abundance of about 73.80%in the initial stage, then Sulfobacillus thermosulfidooxidans dominated from the 18th day to the end of bioleaching, while the abundance of Leptospirillum ferriphilum changed slightly. A higher solution potential within a certain range and appropriate concentration of ferric ions were essential for this tank bioleaching of chalcopyrite. 展开更多
关键词 CHALCOPYRITE tank bioleaching microbial community PCR-RFLP technique
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New Primers for Denaturing Gradient Gel Electrophoresis Analysis of Nitrate-Reducing Bacterial Community in Soil 被引量:2
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作者 R.PASTORELLI R.PICCOLO +1 位作者 S.SIMONCINI S.LANDI 《Pedosphere》 SCIE CAS CSCD 2013年第3期340-349,共10页
The narG gene is frequently used as a molecular marker for bacterial nitrate-reducing community analysis. In this study, a new set of primers targeting the narG gene was designed and applied to semi-nested polymerase ... The narG gene is frequently used as a molecular marker for bacterial nitrate-reducing community analysis. In this study, a new set of primers targeting the narG gene was designed and applied to semi-nested polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) assay. The potential of the new primers was verified on DNA directly extracted from soils from five different experimental sites distributed in Central and Southern Italy. Specificity of the primers was determined by excision, amplification, and sequencing of bands resolved by DGGE. A phylogenetic analysis showed the correlation between the sequences retrieved from the soils studied and the narG sequences from βand y-Proteobacteria. These primers expanded the existing molecular tools for ecological study on the size and diversity of nitrate-reducing bacterial community in soil. 展开更多
关键词 DNA gene sequence narG phylogenetic analysis PROTEOBACTERIA
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Synthesis of photolabile dUTP analogues and their enzymatic incorporation for DNA labeling
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作者 WU JunZhou WANG Jie TANG XinJing 《Science China Chemistry》 SCIE EI CAS 2014年第2期322-328,共7页
Two new photolabile nucleotide analogues with furan-fused deoxyuridine were synthesized through Sonogashira coupling.Their enzymatic incorporation into DNA was evaluated with two DNA polymerases(Taq and Deep vent exo-... Two new photolabile nucleotide analogues with furan-fused deoxyuridine were synthesized through Sonogashira coupling.Their enzymatic incorporation into DNA was evaluated with two DNA polymerases(Taq and Deep vent exo-)by polymerase chain reaction(PCR).Deep vent exo-recognized both nucleotides as substrates for primer extension,while Taq was much less proficient.Light irradiation of PCR products released the amino and carboxyl moieties of DNA.Further labeling with fluorescein isothiocyanate for a long DNA construct with F-dUnTP incorporation was successfully achieved. 展开更多
关键词 photolabile nucleotides enzymatic incorporation nucleotide analogues fluorescent labeling
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