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m tuberculosis h37rv  (ATCC)


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    ATCC m tuberculosis h37rv
    (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.
    M Tuberculosis H37rv, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/m tuberculosis h37rv/product/ATCC
    Average 94 stars, based on 4 article reviews
    m tuberculosis h37rv - by Bioz Stars, 2026-04
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    Images

    1) Product Images from "Direct detection and quantification of Mycobacterium tuberculosis from clinical samples by high-resolution melt qPCR"

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

    Journal: medRxiv

    doi: 10.64898/2026.03.07.26347851

    (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.
    Figure Legend 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.

    Techniques Used: Amplification, Control, Generated



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    m tuberculosis h37rv  (ATCC)
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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.
    M Tuberculosis H37rv, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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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    reference sequence m tuberculosis h37rv  (ATCC)
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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) 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

    The result of Mycobacterium tuberculosis H37Rv (ATCC 27294) using multiplex assay

    Journal: Applied Microbiology and Biotechnology

    Article Title: A multiplex assay based on capillary electrophoresis to detect Mycobacterium tuberculosis complex: development and clinical validation

    doi: 10.1007/s00253-025-13701-0

    Figure Lengend Snippet: The result of Mycobacterium tuberculosis H37Rv (ATCC 27294) using multiplex assay

    Article Snippet: Briefly, they were designed as follows: first, gene sequences were retrieved from NCBI for the following mycobacterium: M. tuberculosis (ATCC 27294), M. marinum (ATCC 927), M. gordonae (ATCC 14470), M. scrofulaceum (ATCC 19981), M. terrae (ATCC 15755), M. fortuitum subsp. fortuitum (ATCC 6841), M. asiaticum (ATCC 25276).

    Techniques: Multiplex Assay

    The location of IS6110 deletion. A Circos plot of the genome of A1 strain. B Alignment of sequence in the location of IS6110 deletion with Mycobacterium tuberculosis H37Rv reference sequence. C Dot plot of the alignment

    Journal: Applied Microbiology and Biotechnology

    Article Title: A multiplex assay based on capillary electrophoresis to detect Mycobacterium tuberculosis complex: development and clinical validation

    doi: 10.1007/s00253-025-13701-0

    Figure Lengend Snippet: The location of IS6110 deletion. A Circos plot of the genome of A1 strain. B Alignment of sequence in the location of IS6110 deletion with Mycobacterium tuberculosis H37Rv reference sequence. C Dot plot of the alignment

    Article Snippet: Briefly, they were designed as follows: first, gene sequences were retrieved from NCBI for the following mycobacterium: M. tuberculosis (ATCC 27294), M. marinum (ATCC 927), M. gordonae (ATCC 14470), M. scrofulaceum (ATCC 19981), M. terrae (ATCC 15755), M. fortuitum subsp. fortuitum (ATCC 6841), M. asiaticum (ATCC 25276).

    Techniques: Sequencing