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反向斑点杂交    
相关语句
  reverse dot blot
    Methods Polymerase chain reaction(PCR) connected with reverse dot blot(RDB) were performed.
    方法采用多聚酶链反应(PCR)结合反向斑点杂交(RDB)技术。
短句来源
    Detection of rpoB mutations in rifampin resistant Mycobacterium tuberculosis strains by the reverse dot blot hybridization method
    应用反向斑点杂交法检测耐利福平结核分支杆菌rpoB基因突变
短句来源
    Rapid identification of mycobacterium species by amplification of rpoB gene and reverse dot blot hybridization assay
    应用rpoB基因PCR反向斑点杂交快速鉴定分枝杆菌菌种的研究
短句来源
    Detection of β-thalassemia by PCR connected with reverse dot blot
    应用PCR结合反向斑点杂交技术检测β-地中海贫血
短句来源
    The 16S rRNA PCR-membrane reverse dot blot hybridization technique showed that the sensitivity was 92.49%, and the specificity was 100%.
    PCR-膜反向斑点杂交技术鉴定分枝杆菌菌种的灵敏度为92.49%,特异度为100%。
短句来源
更多       
  reverse dot blot hybridization
    Detection of rpoB mutations in rifampin resistant Mycobacterium tuberculosis strains by the reverse dot blot hybridization method
    应用反向斑点杂交法检测耐利福平结核分支杆菌rpoB基因突变
短句来源
    Rapid identification of mycobacterium species by amplification of rpoB gene and reverse dot blot hybridization assay
    应用rpoB基因PCR反向斑点杂交快速鉴定分枝杆菌菌种的研究
短句来源
    The 16S rRNA PCR-membrane reverse dot blot hybridization technique showed that the sensitivity was 92.49%, and the specificity was 100%.
    PCR-膜反向斑点杂交技术鉴定分枝杆菌菌种的灵敏度为92.49%,特异度为100%。
短句来源
    Results PCR products from 36 RFP resistant and 22 RFP susceptible isolates were detected by the assay of reverse dot blot hybridization, showing that the susceptibility and the specificity rate were 88.9% and 86.4% respectively,and the coincidence with biochemical method and sequencing is 87.9% and 89.7% respectively.
    结果 应用反向斑点杂交法检测 36株耐药株和 2 2株敏感株rpoB基因的突变位点 ,并据此判断其对利福平的药敏特性 ,结果敏感性为 88.9% ,特异性为 86 .4 % ,药敏结果符合率为 87.9% ,与测序结果的符合率为 89.7%。
短句来源
    Rapid detection of mycoplasma pneumoniae by reverse Dot blot hybridization
    反向斑点杂交法快速检测肺炎支原体
短句来源
更多       
  reverse dot blot hybridization
    Detection of rpoB mutations in rifampin resistant Mycobacterium tuberculosis strains by the reverse dot blot hybridization method
    应用反向斑点杂交法检测耐利福平结核分支杆菌rpoB基因突变
短句来源
    Rapid identification of mycobacterium species by amplification of rpoB gene and reverse dot blot hybridization assay
    应用rpoB基因PCR反向斑点杂交快速鉴定分枝杆菌菌种的研究
短句来源
    The 16S rRNA PCR-membrane reverse dot blot hybridization technique showed that the sensitivity was 92.49%, and the specificity was 100%.
    PCR-膜反向斑点杂交技术鉴定分枝杆菌菌种的灵敏度为92.49%,特异度为100%。
短句来源
    Results PCR products from 36 RFP resistant and 22 RFP susceptible isolates were detected by the assay of reverse dot blot hybridization, showing that the susceptibility and the specificity rate were 88.9% and 86.4% respectively,and the coincidence with biochemical method and sequencing is 87.9% and 89.7% respectively.
    结果 应用反向斑点杂交法检测 36株耐药株和 2 2株敏感株rpoB基因的突变位点 ,并据此判断其对利福平的药敏特性 ,结果敏感性为 88.9% ,特异性为 86 .4 % ,药敏结果符合率为 87.9% ,与测序结果的符合率为 89.7%。
短句来源
    Rapid detection of mycoplasma pneumoniae by reverse Dot blot hybridization
    反向斑点杂交法快速检测肺炎支原体
短句来源
更多       
  reverse dot blot
    Methods Polymerase chain reaction(PCR) connected with reverse dot blot(RDB) were performed.
    方法采用多聚酶链反应(PCR)结合反向斑点杂交(RDB)技术。
短句来源
    Detection of rpoB mutations in rifampin resistant Mycobacterium tuberculosis strains by the reverse dot blot hybridization method
    应用反向斑点杂交法检测耐利福平结核分支杆菌rpoB基因突变
短句来源
    Rapid identification of mycobacterium species by amplification of rpoB gene and reverse dot blot hybridization assay
    应用rpoB基因PCR反向斑点杂交快速鉴定分枝杆菌菌种的研究
短句来源
    Detection of β-thalassemia by PCR connected with reverse dot blot
    应用PCR结合反向斑点杂交技术检测β-地中海贫血
短句来源
    The 16S rRNA PCR-membrane reverse dot blot hybridization technique showed that the sensitivity was 92.49%, and the specificity was 100%.
    PCR-膜反向斑点杂交技术鉴定分枝杆菌菌种的灵敏度为92.49%,特异度为100%。
短句来源
更多       

 

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  reverse dot blot
A reverse dot blot assay for identification of Pratylenchus spp.
      
The reverse dot blot is a technique which can be especially used for the simultaneous identification of various bacteria.
      
The positive samples were analyzed with polymerase chain reaction and reverse dot blot method (PCR-RDB).
      
By a reverse dot blot modification, the expression pattern of such fragments was evaluated.
      
HLA-DRB1 was performed by PCR-SSO reverse dot blot hybridization.
      
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