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- W2354899802 abstract "To develop a real|time PCR based on TaqMan technology using the new MGB probe for detecting Mycobacterium tuberculosis DNA, plasmid containing the sequence of interest was constructed. The efficacy of this assay was evaluated by quantitatively measuring levels of the sequence of interest inserted in the plasmid and by detecting the clinical specimens. The conserved regions of Mycobacterium tuberculosis IS6110 element were chosen as primers and MGB probe. Results showed that this assay for Mycobacterium tuberculosis had a detection limit of one genome copy number per reaction. A linear standard curve was obtained between 10+0 and 10+8 DNA copies per reaction ( r 0 990). The coefficient of variation for both intra| and inter|experimental variability indicated remarkable reproducibility. The sensitivity and specificity of this assay was 100%, respectively. These observations suggested that real|time PCR based on MGB probe was an excellent candidate for the standard method detecting Mycobacterium tuberculosis." @default.
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- W2354899802 date "2003-01-01" @default.
- W2354899802 modified "2023-09-25" @default.
- W2354899802 title "Detection of Mycobacterium Tuberculosis DNA by Real-time Polymerase Chain Reaction using TaqMan-MGB Probe Technology" @default.
- W2354899802 hasPublicationYear "2003" @default.
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