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mycoplasmoides pneumoniae strain m129 b7  (ATCC)


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    ATCC mycoplasmoides pneumoniae strain m129 b7
    Mycoplasmoides Pneumoniae Strain M129 B7, 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
    https://www.bioz.com/product/m129/Quantitative+Genomic%3B+DNA+fromMycoplasma%3B+pneumoniaeStrain%3A+M129-B7/pmc12989572-182-10-14
    Average 94 stars, based on 1 article reviews
    mycoplasmoides pneumoniae strain m129 b7 - by Bioz Stars, 2026-10
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    Related Articles

    other:

    Article Title: Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark
    Article Snippet: M129 (ATCC 29342) , 0.06 , 0.5 , 0.25 , 0.001 , 0.03 , 0.5 , 0.001 , alanine (A) [NC_000912] , adenine (A) [NC_000912].

    Bacteria:

    Article Title: PHEVIR: an artificial intelligence algorithm that predicts the molecular role of pathogens in complex human diseases
    Article Snippet: .. The top five most connected bacteria in the network were Helicobacter pylori (strain ATCC 700392/26695) that is comorbid to 1080 human diseases, Yersinia pestis that is comorbid to 855 human diseases, Staphylococcus aureus that is comorbid to 578 human diseases, Streptococcus pyogenes serotype M1 that is comorbid to 428 human diseases, and Mycoplasma pneumoniae strain ATCC 29342/M129) that is comorbid to 406 human diseases. ..

    Infection:

    Article Title: Nasal delivery of Lacticaseibacillus rhamnosus GG modulates respiratory immune responses and attenuates Mycoplasma pneumoniae pneumonia in a murine model.
    Article Snippet: .. M. pneumoniae preparation and infection The standard strain of M. pneumoniae type 1, M129 (ATCC 29342), was maintained at the Institute of Pathogen Biology, Hengyang Medical College, University of South China. .. This strain was cultivated in a pleuropneumonia-like organism (PPLO) medium (BD Bioscien ces, USA).

    Mutagenesis:

    Article Title: Clinical performance of two commercial PCR assays for the detection of macrolide resistance in Mycoplasma pneumoniae .
    Article Snippet: .. Eight M. pneumoniae strains were used: two wild-type (WT) reference strains, M129 (ATCC 29342) and FH (ATCC 15531); five clinical isolates carrying 23S rRNA mutations (13) from the collection of the Bacteriology Department, Bordeaux University Hospital, France; and one in vitro–selected mutant, E3 (14) (Table 1). .. In addition, 10 strains of other Mycoplasma species were included: Mycoplasma fermentans PG18 (ATCC 19989), Mycoplasma genitalium G37 (ATCC 33530), Mycoplasma hominis PG21 (ATCC 23114), Mycoplasma orale CH 19299 (ATCC 23714), Mycoplasma penetrans GTU54 (ATCC 55252), Mycoplasma salivarium PG20 (ATCC 23064), Ureaplasma parvum S3 (ATCC 27815), Ureaplasma urealyticum S8 (ATCC 27618), 1 WT clinical isolate of Mycoplasma amphor iforme from the Bordeaux University Hospital collection, and 1 M. genitalium in vitro– selected mutant harboring the A2059G substitution (Escherichia coli numbering), mutant J10 (15).



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    ATCC m pneumoniae
    Sensitivity of the LAMP reaction for the detection of S. <t>pneumoniae</t> , S. aureus , H. influenzae , and M. pneumoniae. Visual LoD determined for the detection of S. pneumoniae (3.9 ×10 3 CFU/mL), S. aureus (1.7 ×10 5 CFU/mL), H. influenzae (8.2 ×10 3 CFU/mL), and M. pneumoniae (1.27 ×10 3 genome copies/reaction) (A) . Verification of amplification by 2% agarose gel electrophoresis (B) .
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    m129  (ATCC)
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    ATCC m129
    Sensitivity of the LAMP reaction for the detection of S. <t>pneumoniae</t> , S. aureus , H. influenzae , and M. pneumoniae. Visual LoD determined for the detection of S. pneumoniae (3.9 ×10 3 CFU/mL), S. aureus (1.7 ×10 5 CFU/mL), H. influenzae (8.2 ×10 3 CFU/mL), and M. pneumoniae (1.27 ×10 3 genome copies/reaction) (A) . Verification of amplification by 2% agarose gel electrophoresis (B) .
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    Image Search Results


    Sensitivity of the LAMP reaction for the detection of S. pneumoniae , S. aureus , H. influenzae , and M. pneumoniae. Visual LoD determined for the detection of S. pneumoniae (3.9 ×10 3 CFU/mL), S. aureus (1.7 ×10 5 CFU/mL), H. influenzae (8.2 ×10 3 CFU/mL), and M. pneumoniae (1.27 ×10 3 genome copies/reaction) (A) . Verification of amplification by 2% agarose gel electrophoresis (B) .

    Journal: Frontiers in Microbiology

    Article Title: Development and optimization of an easy to interpret loop-mediated isothermal amplification (LAMP) assay for the identification of bacterial pathogens causing childhood pneumonia

    doi: 10.3389/fmicb.2026.1748456

    Figure Lengend Snippet: Sensitivity of the LAMP reaction for the detection of S. pneumoniae , S. aureus , H. influenzae , and M. pneumoniae. Visual LoD determined for the detection of S. pneumoniae (3.9 ×10 3 CFU/mL), S. aureus (1.7 ×10 5 CFU/mL), H. influenzae (8.2 ×10 3 CFU/mL), and M. pneumoniae (1.27 ×10 3 genome copies/reaction) (A) . Verification of amplification by 2% agarose gel electrophoresis (B) .

    Article Snippet: Initially, tests included panel bacteria: S. pneumoniae ATCC 49619, S. aureus ATCC 25923, H. influenzae ATCC 49766, and purified DNA from M. pneumoniae (ATCC 29342DQ).

    Techniques: Amplification, Agarose Gel Electrophoresis

    Sensitivity of the designed primers for the detection of K. pneumoniae. Visual LoD (A) . The calculated LoD was 1.5 ×10 4 CFU/mL. Amplification was confirmed by 2% agarose gel electrophoresis (B) .

    Journal: Frontiers in Microbiology

    Article Title: Development and optimization of an easy to interpret loop-mediated isothermal amplification (LAMP) assay for the identification of bacterial pathogens causing childhood pneumonia

    doi: 10.3389/fmicb.2026.1748456

    Figure Lengend Snippet: Sensitivity of the designed primers for the detection of K. pneumoniae. Visual LoD (A) . The calculated LoD was 1.5 ×10 4 CFU/mL. Amplification was confirmed by 2% agarose gel electrophoresis (B) .

    Article Snippet: Initially, tests included panel bacteria: S. pneumoniae ATCC 49619, S. aureus ATCC 25923, H. influenzae ATCC 49766, and purified DNA from M. pneumoniae (ATCC 29342DQ).

    Techniques: Amplification, Agarose Gel Electrophoresis

    Relationship between time to positivity and bacterial load for LAMP detection of S. pneumoniae , S. aureus , and H. influenzae . As the bacterial concentration decreased, the time required for detection increased across all three pathogens. For S. pneumoniae , high concentrations produced a clear positive result within 35 min. However, concentrations near the LoD (10 4 and 10 3 CFU/mL) required more than 55 min to be considered positive. Similarly, S. aureus showed a positive signal at 35 min when tested at high concentrations, whereas lower concentrations (around 10 4 CFU/mL) required over 45. In the case of H. influenzae , the highest concentration yielded a visible positive reaction at 25 min, while lower concentrations needed up to 45 min. Transition phase: In all cases, there was a stage where tubes began to show a greenish signal, indicating the onset of positivity, although the color had not yet fully developed to a strong green signal.

    Journal: Frontiers in Microbiology

    Article Title: Development and optimization of an easy to interpret loop-mediated isothermal amplification (LAMP) assay for the identification of bacterial pathogens causing childhood pneumonia

    doi: 10.3389/fmicb.2026.1748456

    Figure Lengend Snippet: Relationship between time to positivity and bacterial load for LAMP detection of S. pneumoniae , S. aureus , and H. influenzae . As the bacterial concentration decreased, the time required for detection increased across all three pathogens. For S. pneumoniae , high concentrations produced a clear positive result within 35 min. However, concentrations near the LoD (10 4 and 10 3 CFU/mL) required more than 55 min to be considered positive. Similarly, S. aureus showed a positive signal at 35 min when tested at high concentrations, whereas lower concentrations (around 10 4 CFU/mL) required over 45. In the case of H. influenzae , the highest concentration yielded a visible positive reaction at 25 min, while lower concentrations needed up to 45 min. Transition phase: In all cases, there was a stage where tubes began to show a greenish signal, indicating the onset of positivity, although the color had not yet fully developed to a strong green signal.

    Article Snippet: Initially, tests included panel bacteria: S. pneumoniae ATCC 49619, S. aureus ATCC 25923, H. influenzae ATCC 49766, and purified DNA from M. pneumoniae (ATCC 29342DQ).

    Techniques: Concentration Assay, Produced