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m tuberculosis reference strain h37rv  (ATCC)


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    ATCC m tuberculosis reference strain h37rv
    M Tuberculosis Reference Strain H37rv, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3078 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/m+tuberculosis+reference+strain+h37rv/Mycobacterium+tuberculosis+subsp%2E+tuberculosis/pmc12607706-89-12-17
    Average 99 stars, based on 3078 article reviews
    m tuberculosis reference strain h37rv - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Biomarker Discovery:

    Article Title: Off-label evaluation of the BD MAX MDR-TB assay for rapid diagnosis of rifampicin and isoniazid resistance of Mycobacterium tuberculosis clinical isolates in a high-volume reference laboratory.
    Article Snippet: .. Retrospective validation of the BD MAX MDR-TB assay Initially, the BD MAX assay was validated on cultured isolates using the M. tuberculosis reference strain H37Rv (ATCC 27294) to determine its limit of detection (LoD), the optimal volume of inactivated isolates to be processed, and the required incubation time with the sample treatment reagent (STR), which is a BD MAX’s kit reagent that reduces MTBC viability. ..

    Cell Culture:

    Article Title: Off-label evaluation of the BD MAX MDR-TB assay for rapid diagnosis of rifampicin and isoniazid resistance of Mycobacterium tuberculosis clinical isolates in a high-volume reference laboratory.
    Article Snippet: .. Retrospective validation of the BD MAX MDR-TB assay Initially, the BD MAX assay was validated on cultured isolates using the M. tuberculosis reference strain H37Rv (ATCC 27294) to determine its limit of detection (LoD), the optimal volume of inactivated isolates to be processed, and the required incubation time with the sample treatment reagent (STR), which is a BD MAX’s kit reagent that reduces MTBC viability. ..

    Article Title: Off-label evaluation of the BD MAX MDR-TB assay for rapid diagnosis of rifampicin and isoniazid resistance of Mycobacterium tuberculosis clinical isolates in a high-volume reference laboratory
    Article Snippet: .. Initially, the BD MAX assay was validated on cultured isolates using the M. tuberculosis reference strain H37Rv (ATCC 27294) to determine its limit of detection (LoD), the optimal volume of inactivated isolates to be processed, and the required incubation time with the sample treatment reagent (STR), which is a BD MAX’s kit reagent that reduces MTBC viability. ..

    Incubation:

    Article Title: Off-label evaluation of the BD MAX MDR-TB assay for rapid diagnosis of rifampicin and isoniazid resistance of Mycobacterium tuberculosis clinical isolates in a high-volume reference laboratory.
    Article Snippet: .. Retrospective validation of the BD MAX MDR-TB assay Initially, the BD MAX assay was validated on cultured isolates using the M. tuberculosis reference strain H37Rv (ATCC 27294) to determine its limit of detection (LoD), the optimal volume of inactivated isolates to be processed, and the required incubation time with the sample treatment reagent (STR), which is a BD MAX’s kit reagent that reduces MTBC viability. ..

    Article Title: Off-label evaluation of the BD MAX MDR-TB assay for rapid diagnosis of rifampicin and isoniazid resistance of Mycobacterium tuberculosis clinical isolates in a high-volume reference laboratory
    Article Snippet: .. Initially, the BD MAX assay was validated on cultured isolates using the M. tuberculosis reference strain H37Rv (ATCC 27294) to determine its limit of detection (LoD), the optimal volume of inactivated isolates to be processed, and the required incubation time with the sample treatment reagent (STR), which is a BD MAX’s kit reagent that reduces MTBC viability. ..

    In Vitro:

    Article Title: Molecular Bacterial Load Assay Concurs with Culture on NaOH-Induced Loss of Mycobacterium tuberculosis Viability
    Article Snippet: .. Laboratory experiments were performed using five replicates of M. tuberculosis reference strain H37Rv (ATCC 27294) and pooled sputum samples from pulmonary TB patients at the National Institute for Medical Research, Medical Research Centre (NIMR-MMRC), Mbeya, Tanzania ( and ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG 1 caption a7 Flow diagram of laboratory experiments, conditions, and downstream tests performed for M. tuberculosis cultures and sputum specimens. (A) In vitro experimental procedure employed for each decontaminated M. tuberculosis (Mtb) culture. (B) Experimental flow for pooled patient sputum specimens. ..

    other:

    Article Title: Involvement of Vasopressin in the Pathogenesis of Pulmonary Tuberculosis: A New Therapeutic Target?
    Article Snippet: Briefly, the M. tuberculosis reference strain H37Rv (ATCC No. 25618) was grown in Middlebrook 7H9 broth (DIFCO) supplemented with 0.2% glycerol, 10% OADC enrichment, and 0.02% Tween-80 and maintained at 37°C in agitation.



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    m tuberculosis reference strain h37rv  (ATCC)
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    Time–kill curves of aldoxorubicin (A), quarfloxin (B), and INH (C) against Mtb <t>H37Rv.</t> Antibiotic concentrations are presented as different symbols. The INH was used as a positive control.
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    Time–kill curves of aldoxorubicin (A), quarfloxin (B), and INH (C) against Mtb H37Rv. Antibiotic concentrations are presented as different symbols. The INH was used as a positive control.

    Journal: Briefings in Bioinformatics

    Article Title: Machine learning–enabled virtual screening indicates the anti-tuberculosis activity of aldoxorubicin and quarfloxin with verification by molecular docking, molecular dynamics simulations, and biological evaluations

    doi: 10.1093/bib/bbae696

    Figure Lengend Snippet: Time–kill curves of aldoxorubicin (A), quarfloxin (B), and INH (C) against Mtb H37Rv. Antibiotic concentrations are presented as different symbols. The INH was used as a positive control.

    Article Snippet: The M. tuberculosis reference strain H37Rv ATCC27294 was obtained from the American Type Culture Collection.

    Techniques: Positive Control

    The intracellular survival rate of Mtb H37Rv after aldoxorubicin and quarfloxin exposure. (A) Aldoxorubicin group: infected macrophages treated with aldoxorubicin at 1× MIC, 2× MIC, and 4× MIC. (B) Quarfloxin group: infected macrophages treated with quarfloxin at 1× MIC, 2× MIC, and 4× MIC. The INH group served as the positive control. * * * P < .001.

    Journal: Briefings in Bioinformatics

    Article Title: Machine learning–enabled virtual screening indicates the anti-tuberculosis activity of aldoxorubicin and quarfloxin with verification by molecular docking, molecular dynamics simulations, and biological evaluations

    doi: 10.1093/bib/bbae696

    Figure Lengend Snippet: The intracellular survival rate of Mtb H37Rv after aldoxorubicin and quarfloxin exposure. (A) Aldoxorubicin group: infected macrophages treated with aldoxorubicin at 1× MIC, 2× MIC, and 4× MIC. (B) Quarfloxin group: infected macrophages treated with quarfloxin at 1× MIC, 2× MIC, and 4× MIC. The INH group served as the positive control. * * * P < .001.

    Article Snippet: The M. tuberculosis reference strain H37Rv ATCC27294 was obtained from the American Type Culture Collection.

    Techniques: Infection, Positive Control