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mycobacterium tuberculosis h37rv  (ATCC)


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    ATCC mycobacterium tuberculosis h37rv
    Mycobacterium Tuberculosis H37rv, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3090 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/h37rv/Mycobacterium+tuberculosis+subsp%2E+tuberculosis/pm42250355-79-40-43
    Average 99 stars, based on 3090 article reviews
    mycobacterium tuberculosis h37rv - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Serial Dilution:

    Article Title: Evaluation of the Simple One-Step (SOS) stool method for Truenat MTB plus and Xpert MTB/XDR assay.
    Article Snippet: .. Preparation of MTB serial dilution suspensions Four MTB serial dilution suspensions were prepared using the well-characterized H37Rv (ATCC 27294) strain that had been grown on the mycobacteria growth indicator tube (MGIT) media. ..

    Control:

    Article Title: Effects of mutations in multiple Ethionamide-resistance-associated genes among Mycobacterium tuberculosis clinical isolates from China
    Article Snippet: DST was performed to determine the MICs of ETH for each isolate, using Sensititre ® plates (Thermo Fisher Scientific Inc., Cleveland, Ohio, USA). .. All procedures were carried out in accordance with the manufacturer’s instructions, and H37Rv (ATCC 27294) was included as a quality control strain in each batch of DST. ..

    Article Title: Early detection of drug-resistant mycobacterium tuberculosis
    Article Snippet: .. The laboratory strain, H37Rv (ATCC 27294), was used as a susceptible control and the M. tuberculosis strain (BCCM/ITM 121749), obtained from Belgium coordinated collection of micro-organisms (A63P mutation in atpE) was used as a resistant control. ..

    other:

    Article Title: Discrimination between Mycobacterium tuberculosis and Mycobacterium bovis using Fourier transform infrared spectroscopy
    Article Snippet: , H37Rv (ATCC 27294) , Human , L4 , FMVZ, USP , –.


    Amplification:

    Article Title: CDK1-induced regulation of p53 phosphorylation at Ser315 mediates cell cycle arrest and apoptosis of macrophages infected with clinical isolates of Mycobacterium tuberculosis
    Article Snippet: .. In addition, 50–100 μl frozen H37Rv (cat. no. 27294; American Type Culture Collection) bacterial solution was aspirated, added to 40 ml Mycobacterium liquid medium and amplified by shaking at 120 rpm. ..

    Mutagenesis:

    Article Title: Early detection of drug-resistant mycobacterium tuberculosis
    Article Snippet: .. The laboratory strain, H37Rv (ATCC 27294), was used as a susceptible control and the M. tuberculosis strain (BCCM/ITM 121749), obtained from Belgium coordinated collection of micro-organisms (A63P mutation in atpE) was used as a resistant control. ..



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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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    Image Search Results


    (A) LCD4.G, LCD4.C, and LCD4.D T cell lines responses to M. tuberculosis (mTB son), M. leprae (mLEP son), M. smegmatis (mSMEG) and non-mycobacterial lysates. (B) LCD4.G and LCD4.CD T cell lines were tested for recognition of known CD1-presented antigens, including dideoxymycobactin (DDM), glucose monomycolate (GMM), mycolic acid, mannose-capped lipoarabinomannan (manLAM), and mannosyl phosphodolichol (MPD). (C) Effect of proteinase K and heat treatment of the M. tuberculosis Triton X-114 extract on T cell proliferation. TX-114 extract was added to the T cell assay after one of four treatments: untreated; proteinase K treatment followed by heat inactivation; heat treatment alone; or incubation with heat-inactivated proteinase K. Data indicate mean ± SEM of triplicate values and are representative of three independent experiments (A–C).

    Journal: bioRxiv

    Article Title: CD1a-Mediated Presentation of Canonical Microbial Peptides to T Cells

    doi: 10.64898/2026.05.05.723095

    Figure Lengend Snippet: (A) LCD4.G, LCD4.C, and LCD4.D T cell lines responses to M. tuberculosis (mTB son), M. leprae (mLEP son), M. smegmatis (mSMEG) and non-mycobacterial lysates. (B) LCD4.G and LCD4.CD T cell lines were tested for recognition of known CD1-presented antigens, including dideoxymycobactin (DDM), glucose monomycolate (GMM), mycolic acid, mannose-capped lipoarabinomannan (manLAM), and mannosyl phosphodolichol (MPD). (C) Effect of proteinase K and heat treatment of the M. tuberculosis Triton X-114 extract on T cell proliferation. TX-114 extract was added to the T cell assay after one of four treatments: untreated; proteinase K treatment followed by heat inactivation; heat treatment alone; or incubation with heat-inactivated proteinase K. Data indicate mean ± SEM of triplicate values and are representative of three independent experiments (A–C).

    Article Snippet: The M. tuberculosis (H37Rv) Triton X-114 extracted proteins (50 mg) were lyophilized with 7.25 M PlusOne urea (Fisher), 0.4% 3-10 ZOOM carrier ampholytes (ThermoFisher), 1.6% 4-7 pharmalytes, 1% N-octylthioglucoside (EMD Chemicals, Inc) and 2 mM DL-Dithiothreitol (DTT, Fisher).

    Techniques: Incubation

    (A) The M. tuberculosis Triton X-114 extract was subjected to preparative IEF, and each fraction was analyzed by Western blot and screened for T cell activation. (B) Identification of candidate proteins by proteomic analysis (LC–MS/MS) of the active fractions. Active fractions stimulating each T cell line were identified by T cell “Western blot” assay. (C) Proliferative response of LCD4.G to purified recombinant lipoproteins derived from the 25-kDa M. tuberculosis lipoglycoprotein LppX. mTB son, M. tuberculosis sonicated. mSMEG, M. smegmatis . Data indicate mean of triplicate values for LCD4.G T cell line and are representative of three independent experiments (A–C). See also Figures S2 and S5.

    Journal: bioRxiv

    Article Title: CD1a-Mediated Presentation of Canonical Microbial Peptides to T Cells

    doi: 10.64898/2026.05.05.723095

    Figure Lengend Snippet: (A) The M. tuberculosis Triton X-114 extract was subjected to preparative IEF, and each fraction was analyzed by Western blot and screened for T cell activation. (B) Identification of candidate proteins by proteomic analysis (LC–MS/MS) of the active fractions. Active fractions stimulating each T cell line were identified by T cell “Western blot” assay. (C) Proliferative response of LCD4.G to purified recombinant lipoproteins derived from the 25-kDa M. tuberculosis lipoglycoprotein LppX. mTB son, M. tuberculosis sonicated. mSMEG, M. smegmatis . Data indicate mean of triplicate values for LCD4.G T cell line and are representative of three independent experiments (A–C). See also Figures S2 and S5.

    Article Snippet: The M. tuberculosis (H37Rv) Triton X-114 extracted proteins (50 mg) were lyophilized with 7.25 M PlusOne urea (Fisher), 0.4% 3-10 ZOOM carrier ampholytes (ThermoFisher), 1.6% 4-7 pharmalytes, 1% N-octylthioglucoside (EMD Chemicals, Inc) and 2 mM DL-Dithiothreitol (DTT, Fisher).

    Techniques: Western Blot, Activation Assay, Liquid Chromatography with Mass Spectroscopy, Purification, Recombinant, Derivative Assay, Sonication

    (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