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m tuberculosis h37ra  (ATCC)


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    Structured Review

    ATCC m tuberculosis h37ra
    M Tuberculosis H37ra, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 136 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mycobacterium+tuberculosis+strain/Genomic+DNA+from+Mycobacterium+tuberculosis+strain+H37Ra/pm42217400-54-3-6
    Average 93 stars, based on 136 article reviews
    m tuberculosis h37ra - by Bioz Stars, 2026-09
    93/100 stars

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    other:

    Article Title: Evaluation of in vitro susceptibility to sparteine in four strains of Mycobacterium tuberculosis
    Article Snippet: Mycobacterium tuberculosis strain resistant to isoniazid (ATCC 35822).

    Article Title: Evaluation of in vitro susceptibility to sparteine in four strains of Mycobacterium tuberculosis
    Article Snippet: The strains used were: Mycobacterium tuberculosis strain sensitive to isoniazid and rifampicin H37Rv (ATCC 27294).

    Article Title: Evaluation of in vitro susceptibility to sparteine in four strains of Mycobacterium tuberculosis
    Article Snippet: Mycobacterium tuberculosis strain resistant to rifampicin (ATCC 35838).

    Article Title: In vitro, evaluation of anti-mycobacterial active plant extracts against Mycobacterium tuberculosis using BACTEC mycobacteria growth indicator tube 960 automated system
    Article Snippet: 3.3 Mycobacterium tuberculosis strain and culture medium H37Rv (ATCC 25618) was used as a reference strain for the anti-mycobacterial assay, Mtb culture with DMSO (1.2%), Isoniazid (INH) at MIC99 (0.05 μg/mL) and Rifampicin (RIF) at MIC99 (0.12 μg/mL) were used as controls.

    Article Title: Evolution of the Natural Transformation Protein, ComEC, in Bacteria
    Article Snippet: Kyoto strain=Kyoto' 'Azorhizobium caulinodans ORS 571 strain=ORS 571' 'Streptococcus pyogenes strain=NS53' 'Dickeya zeae EC1 strain=EC1' 'Clostridioides difficile strain=630Derm' 'Calothrix sp. 3363 strain=3363' 'Bacillus selenitireducens MLS10 strain=MLS10' 'Acinetobacter baumannii D1279779 strain=D1279779' 'Devosia sp. H5989 strain=H5989' 'Helicobacter pylori HPAG1 strain=HPAG1' 'Bacteroides fragilis strain=BOB25' 'Campylobacter jejuni subsp. jejuni strain=35925' 'Pseudomonas sp. L10.10 strain=L10.10' 'Chlamydia psittaci WSRTE30 strain=WSRTE30' 'Streptococcus suis SC84 strain=SC84' 'Rhodovulum sulfidophilum DSM 1374 strain=DSM 1374' 'Acidithiobacillus caldus ATCC 51756 strain=ATCC 51756' 'Nocardia cyriacigeorgica GUH-2 strain=GUH-2' 'Citrobacter sp. FDAARGOS 156 strain=FDAARGOS 155' 'Xanthomonas fragariae' 'Bacillus amyloliquefaciens UMAF6639 strain=UMAF6639' 'Streptococcus equi subsp. zooepidemicus MGCS10565 strain=MGCS10565 ATCC BAA1716' 'Filifactor alocis ATCC 35896 strain=ATCC 35896' 'Roseiflexus castenholzii DSM 13941 strain=DSM 13941' 'Thermoanaerobacter kivui strain=LKT-1' 'Carnobacterium maltaromaticum LMA28 strain=LMA28' 'Acidaminococcus intestini RyC-MR95 strain=RyC-MR95' 'Vibrio campbellii ATCC BAA-1116 strain=ATCC BAA-1116 BB120' 'Fusobacterium hwasookii ChDC F300 strain=ChDC F300' 'Novosphingobium pentaromativorans US6-1 strain=US6-1' 'Streptomyces albus strain=BK3-25' 'Altererythrobacter atlanticus strain=26DY36' 'Lactobacillus heilongjiangensis strain=DSM 28069' 'Candidatus Paracaedibacter acanthamoebae' 'Syntrophobotulus glycolicus DSM 8271 strain=DSM 8271' 'Neorickettsia helminthoeca str.

    Activity Assay:

    Article Title: Design, synthesis, in silico studies, and evaluation of novel chalcones and their pyrazoline derivatives for antibacterial and antitubercular activities
    Article Snippet: A new series of naphthyl chalcones (3a–3p) and their pyrazoline derivatives (4a–4h) were synthesized using substituted acetophenones, substituted naphthaldehydes, and hydrazine hydrate as starting materials.. All the synthesized compounds were characterized by IR, NMR, and mass spectrometric analysis and screened for antimycobacterial activity against Mycobacterium tuberculosis H37Rv (ATCC 27924) and antibacterial activity against Staphylococcus aureus (MTCC 96), Bacillus subtilis (MTCC 441), Escherichia coli (MTCC 443) and Klebsiella pneumonia (MTCC 109).. Compounds 3b and 3p exhibited significant antibacterial activity against all the tested bacterial strains.

    Synthesized:

    Article Title: Design, synthesis, in silico studies, and evaluation of novel chalcones and their pyrazoline derivatives for antibacterial and antitubercular activities
    Article Snippet: A new series of naphthyl chalcones (3a–3p) and their pyrazoline derivatives (4a–4h) were synthesized using substituted acetophenones, substituted naphthaldehydes, and hydrazine hydrate as starting materials.. All the synthesized compounds were characterized by IR, NMR, and mass spectrometric analysis and screened for antimycobacterial activity against Mycobacterium tuberculosis H37Rv (ATCC 27924) and antibacterial activity against Staphylococcus aureus (MTCC 96), Bacillus subtilis (MTCC 441), Escherichia coli (MTCC 443) and Klebsiella pneumonia (MTCC 109).. Compounds 3b and 3p exhibited significant antibacterial activity against all the tested bacterial strains.

    Growth Inhibition Assay:

    Article Title: Design, synthesis, in silico studies, and evaluation of novel chalcones and their pyrazoline derivatives for antibacterial and antitubercular activities
    Article Snippet: A new series of naphthyl chalcones (3a–3p) and their pyrazoline derivatives (4a–4h) were synthesized using substituted acetophenones, substituted naphthaldehydes, and hydrazine hydrate as starting materials.. All the synthesized compounds were characterized by IR, NMR, and mass spectrometric analysis and screened for antimycobacterial activity against Mycobacterium tuberculosis H37Rv (ATCC 27924) and antibacterial activity against Staphylococcus aureus (MTCC 96), Bacillus subtilis (MTCC 441), Escherichia coli (MTCC 443) and Klebsiella pneumonia (MTCC 109).. Compounds 3b and 3p exhibited significant antibacterial activity against all the tested bacterial strains.

    Alamar Blue Assay:

    Article Title: Novel stilbene scaffolds efficiently target Mycobacterium tuberculosis nucleoid-associated protein, HU
    Article Snippet: Novel scaffolds of stilbene were identified as inhibitors of Mycobacterium tuberculosis by targeting the nucleoid-associated protein, HU, using molecular docking.. Based on the proposed combinatorial libraries I to VI, structures I and III had significantly greater docking binding energy that was comparable to that of the reference ligand, protein HU, from Mycobacterium tuberculosis.. Using these docking results, 18 compounds were synthesized, characterized and evaluated for in vitro antitubercular (anti-TB) efficacy in the Mycobacterium tuberculosis strain, H37Rv.



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    (A) Amplification plot of <t>H37Rv</t> replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.
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    (A) Amplification plot of <t>H37Rv</t> replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.
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    (A) Amplification plot of <t>H37Rv</t> replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.
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    (A) Amplification plot of <t>H37Rv</t> replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.
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    (A) Amplification plot of <t>H37Rv</t> replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.
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    ATCC m tuberculosis h37rv strain
    (A) Amplification plot of <t>H37Rv</t> replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.
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    (A) Amplification plot of H37Rv replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.

    Journal: medRxiv

    Article Title: Direct detection and quantification of Mycobacterium tuberculosis from clinical samples by high-resolution melt qPCR

    doi: 10.64898/2026.03.07.26347851

    Figure Lengend Snippet: (A) Amplification plot of H37Rv replicates targeting the RD9 gene. (B) Corresponding melt curve showing a specific melting temperature (Tm) of ∼75°C. H37Rv DNA was serially diluted from 10 6 to 10 1 copies per reaction and analysed in triplicate. (C) Amplification plot obtained after 40 cycles for the dilutions, including the no-template control (NTC). (D) Corresponding melt curve showing a Tm of 73.7 ± 0.12°C. (E) Standard curve generated from the 10-fold serial dilutions, plotting cycle threshold (Ct) versus log copy number per reaction.

    Article Snippet: Using the M. tuberculosis H37Rv (ATCC #25618DQ) reference strain, we performed asymmetric PCR with Vent (exo-) DNA polymerase (New England Biolabs).

    Techniques: Amplification, Control, Generated