mas (capitalbio molecule annotation system v 4.0) Search Results


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CapitalBio Corporation mas (capitalbio molecule annotation system v 4.0)
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium <t>tuberculosis</t> ; NTM:non-tuberculous mycobacteria.
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Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium tuberculosis ; NTM:non-tuberculous mycobacteria.

Journal: BMC Microbiology

Article Title: Prevalence of nontuberculous mycobacteria in a tertiary hospital in Beijing, China, January 2013 to December 2018

doi: 10.1186/s12866-020-01840-5

Figure Lengend Snippet: Distribution of Positive specimens in Mycobacterium nucleic acid detection during 2013–2018. MTB: Mycobacterium tuberculosis ; NTM:non-tuberculous mycobacteria.

Article Snippet: PCR amplification system was performed according to the manufacturer’s instructions of Tuberculosis and Non-Tuberculous Mycobacteria Real-time PCR Detection Kit (CapitalBio Technology Inc., Beijing, China) [ ] and was roughly as follows; 18 μL PCR amplification reagent and 2 μL template DNA were mixed together; amplification conditions: 37 °C for 5 min, 94 °C for 3 min, and followed by the amplification of 40 cycles of 94 °C for 15 s, 60 °C for 30 s, then 50 °C for 10 s. FAM and HEX channels were selected for fluorescence detection at the same time.

Techniques: