7h10 agar Difco Search Results


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  • 95
    Difco middlebrook 7h10 agar
    Middlebrook 7h10 Agar, supplied by Difco, used in various techniques. Bioz Stars score: 95/100, based on 466 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 95 stars, based on 466 article reviews
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    95
    Difco 7h10 agar plates
    7h10 Agar Plates, supplied by Difco, used in various techniques. Bioz Stars score: 95/100, based on 205 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/7h10 agar plates/product/Difco
    Average 95 stars, based on 205 article reviews
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    94
    Becton Dickinson middlebrook 7h10 agar
    Middlebrook 7h10 Agar, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 94/100, based on 305 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 305 article reviews
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    97
    Difco 7h10 agar medium
    7h10 Agar Medium, supplied by Difco, used in various techniques. Bioz Stars score: 97/100, based on 117 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    7h10 agar medium - by Bioz Stars, 2020-01
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    94
    Becton Dickinson 7h10 agar plates
    7h10 Agar Plates, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 94/100, based on 141 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 141 article reviews
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    88
    Difco 7h10 bacto agar
    7h10 Bacto Agar, supplied by Difco, used in various techniques. Bioz Stars score: 88/100, based on 25 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    84
    Difco 7h10 agar m7h10
    7h10 Agar M7h10, supplied by Difco, used in various techniques. Bioz Stars score: 84/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    84
    Difco solid 7h10 agar
    Isolation and visualization of viable mycobacteria in the RASC. (A) M . smegmatis :: gfp growth on solid <t>7H10</t> agar plates from the Six-Stage Viable Andersen Cascade Impactor after wet release of 200 μl diluted culture into the RASC (30 000, 3000 and 300 colony forming units—CFU). The columns indicate the particle sizes captured on each plate across the 6 stages of the impactor, and the rows indicate the estimated total number of CFU passing through the impactor. Each release was repeated three times and the mean and SD for each plate are presented below the typical growth pattern distribution seen in the particle release. In all the releases the sampling was run for 5 minutes at 28 l/min resulting in the potential total capture of 3000, 300 and 30 CFU respectively. (B) SEM (left) and fluorescent microscopy (right) of M . smegmatis :: gfp isolated on a PM10 impactor following experimental release.
    Solid 7h10 Agar, supplied by Difco, used in various techniques. Bioz Stars score: 84/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    solid 7h10 agar - by Bioz Stars, 2020-01
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    81
    Becton Dickinson 7h10 agar complete medium
    Isolation and visualization of viable mycobacteria in the RASC. (A) M . smegmatis :: gfp growth on solid <t>7H10</t> agar plates from the Six-Stage Viable Andersen Cascade Impactor after wet release of 200 μl diluted culture into the RASC (30 000, 3000 and 300 colony forming units—CFU). The columns indicate the particle sizes captured on each plate across the 6 stages of the impactor, and the rows indicate the estimated total number of CFU passing through the impactor. Each release was repeated three times and the mean and SD for each plate are presented below the typical growth pattern distribution seen in the particle release. In all the releases the sampling was run for 5 minutes at 28 l/min resulting in the potential total capture of 3000, 300 and 30 CFU respectively. (B) SEM (left) and fluorescent microscopy (right) of M . smegmatis :: gfp isolated on a PM10 impactor following experimental release.
    7h10 Agar Complete Medium, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 81/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    81
    Difco middlebrook 7h10 bacto agar
    Isolation and visualization of viable mycobacteria in the RASC. (A) M . smegmatis :: gfp growth on solid <t>7H10</t> agar plates from the Six-Stage Viable Andersen Cascade Impactor after wet release of 200 μl diluted culture into the RASC (30 000, 3000 and 300 colony forming units—CFU). The columns indicate the particle sizes captured on each plate across the 6 stages of the impactor, and the rows indicate the estimated total number of CFU passing through the impactor. Each release was repeated three times and the mean and SD for each plate are presented below the typical growth pattern distribution seen in the particle release. In all the releases the sampling was run for 5 minutes at 28 l/min resulting in the potential total capture of 3000, 300 and 30 CFU respectively. (B) SEM (left) and fluorescent microscopy (right) of M . smegmatis :: gfp isolated on a PM10 impactor following experimental release.
    Middlebrook 7h10 Bacto Agar, supplied by Difco, used in various techniques. Bioz Stars score: 81/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/middlebrook 7h10 bacto agar/product/Difco
    Average 81 stars, based on 4 article reviews
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    middlebrook 7h10 bacto agar - by Bioz Stars, 2020-01
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    83
    Difco 7h10 solid agar medium
    Isolation and visualization of viable mycobacteria in the RASC. (A) M . smegmatis :: gfp growth on solid <t>7H10</t> agar plates from the Six-Stage Viable Andersen Cascade Impactor after wet release of 200 μl diluted culture into the RASC (30 000, 3000 and 300 colony forming units—CFU). The columns indicate the particle sizes captured on each plate across the 6 stages of the impactor, and the rows indicate the estimated total number of CFU passing through the impactor. Each release was repeated three times and the mean and SD for each plate are presented below the typical growth pattern distribution seen in the particle release. In all the releases the sampling was run for 5 minutes at 28 l/min resulting in the potential total capture of 3000, 300 and 30 CFU respectively. (B) SEM (left) and fluorescent microscopy (right) of M . smegmatis :: gfp isolated on a PM10 impactor following experimental release.
    7h10 Solid Agar Medium, supplied by Difco, used in various techniques. Bioz Stars score: 83/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    78
    Difco 7h10 agar media
    a) M. smegmatis , M. abscessus , M. fortuitum subsp. fortuitum , M. chelonae , and M. goodii were patched onto <t>7H10</t> agar media (Difco) at pH 7.0, 6.0, 5.5 or 5.0 to determine pigment production . b) M. avium intracellulare and M. avium subsps. avium were patched onto 7H10 agar media at pH 7.0, 6.0, and 5.5 to determine pigment production. c) From left to right: acetone only, M. smegmatis pH 7.0 extracted w/acetone, M. smegmatis pH 6.0 extracted w/acetone, M. smegmatis pH 5.5 extracted with acetone. d) Fluorescence specific activity units of M. smegmatis bearing empty reporter plasmid pFPV27 or the M. smegmatis probable carotenoid promoter upstream of gfp ( pCar ) at pH 7.0, 6.0 or 5.5.
    7h10 Agar Media, supplied by Difco, used in various techniques. Bioz Stars score: 78/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    81
    Difco middlebrooks 7h10 agar medium
    a) M. smegmatis , M. abscessus , M. fortuitum subsp. fortuitum , M. chelonae , and M. goodii were patched onto <t>7H10</t> agar media (Difco) at pH 7.0, 6.0, 5.5 or 5.0 to determine pigment production . b) M. avium intracellulare and M. avium subsps. avium were patched onto 7H10 agar media at pH 7.0, 6.0, and 5.5 to determine pigment production. c) From left to right: acetone only, M. smegmatis pH 7.0 extracted w/acetone, M. smegmatis pH 6.0 extracted w/acetone, M. smegmatis pH 5.5 extracted with acetone. d) Fluorescence specific activity units of M. smegmatis bearing empty reporter plasmid pFPV27 or the M. smegmatis probable carotenoid promoter upstream of gfp ( pCar ) at pH 7.0, 6.0 or 5.5.
    Middlebrooks 7h10 Agar Medium, supplied by Difco, used in various techniques. Bioz Stars score: 81/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    70
    Difco oadc enriched 7h10 agar medium
    a) M. smegmatis , M. abscessus , M. fortuitum subsp. fortuitum , M. chelonae , and M. goodii were patched onto <t>7H10</t> agar media (Difco) at pH 7.0, 6.0, 5.5 or 5.0 to determine pigment production . b) M. avium intracellulare and M. avium subsps. avium were patched onto 7H10 agar media at pH 7.0, 6.0, and 5.5 to determine pigment production. c) From left to right: acetone only, M. smegmatis pH 7.0 extracted w/acetone, M. smegmatis pH 6.0 extracted w/acetone, M. smegmatis pH 5.5 extracted with acetone. d) Fluorescence specific activity units of M. smegmatis bearing empty reporter plasmid pFPV27 or the M. smegmatis probable carotenoid promoter upstream of gfp ( pCar ) at pH 7.0, 6.0 or 5.5.
    Oadc Enriched 7h10 Agar Medium, supplied by Difco, used in various techniques. Bioz Stars score: 70/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Isolation and visualization of viable mycobacteria in the RASC. (A) M . smegmatis :: gfp growth on solid 7H10 agar plates from the Six-Stage Viable Andersen Cascade Impactor after wet release of 200 μl diluted culture into the RASC (30 000, 3000 and 300 colony forming units—CFU). The columns indicate the particle sizes captured on each plate across the 6 stages of the impactor, and the rows indicate the estimated total number of CFU passing through the impactor. Each release was repeated three times and the mean and SD for each plate are presented below the typical growth pattern distribution seen in the particle release. In all the releases the sampling was run for 5 minutes at 28 l/min resulting in the potential total capture of 3000, 300 and 30 CFU respectively. (B) SEM (left) and fluorescent microscopy (right) of M . smegmatis :: gfp isolated on a PM10 impactor following experimental release.

    Journal: PLoS ONE

    Article Title: Real-Time Investigation of Tuberculosis Transmission: Developing the Respiratory Aerosol Sampling Chamber (RASC)

    doi: 10.1371/journal.pone.0146658

    Figure Lengend Snippet: Isolation and visualization of viable mycobacteria in the RASC. (A) M . smegmatis :: gfp growth on solid 7H10 agar plates from the Six-Stage Viable Andersen Cascade Impactor after wet release of 200 μl diluted culture into the RASC (30 000, 3000 and 300 colony forming units—CFU). The columns indicate the particle sizes captured on each plate across the 6 stages of the impactor, and the rows indicate the estimated total number of CFU passing through the impactor. Each release was repeated three times and the mean and SD for each plate are presented below the typical growth pattern distribution seen in the particle release. In all the releases the sampling was run for 5 minutes at 28 l/min resulting in the potential total capture of 3000, 300 and 30 CFU respectively. (B) SEM (left) and fluorescent microscopy (right) of M . smegmatis :: gfp isolated on a PM10 impactor following experimental release.

    Article Snippet: For the pilot TB studies, the Andersen impactor contained solid 7H10 agar (Difco) plates supplemented with 0.2% glycerol and oleic acid/albumin/dextrose/catalase (OADC) complex.

    Techniques: Isolation, Sampling, Microscopy

    a) M. smegmatis , M. abscessus , M. fortuitum subsp. fortuitum , M. chelonae , and M. goodii were patched onto 7H10 agar media (Difco) at pH 7.0, 6.0, 5.5 or 5.0 to determine pigment production . b) M. avium intracellulare and M. avium subsps. avium were patched onto 7H10 agar media at pH 7.0, 6.0, and 5.5 to determine pigment production. c) From left to right: acetone only, M. smegmatis pH 7.0 extracted w/acetone, M. smegmatis pH 6.0 extracted w/acetone, M. smegmatis pH 5.5 extracted with acetone. d) Fluorescence specific activity units of M. smegmatis bearing empty reporter plasmid pFPV27 or the M. smegmatis probable carotenoid promoter upstream of gfp ( pCar ) at pH 7.0, 6.0 or 5.5.

    Journal: BMC Research Notes

    Article Title: Acidochromogenicity is a common characteristic in nontuberculous mycobacteria

    doi: 10.1186/1756-0500-4-466

    Figure Lengend Snippet: a) M. smegmatis , M. abscessus , M. fortuitum subsp. fortuitum , M. chelonae , and M. goodii were patched onto 7H10 agar media (Difco) at pH 7.0, 6.0, 5.5 or 5.0 to determine pigment production . b) M. avium intracellulare and M. avium subsps. avium were patched onto 7H10 agar media at pH 7.0, 6.0, and 5.5 to determine pigment production. c) From left to right: acetone only, M. smegmatis pH 7.0 extracted w/acetone, M. smegmatis pH 6.0 extracted w/acetone, M. smegmatis pH 5.5 extracted with acetone. d) Fluorescence specific activity units of M. smegmatis bearing empty reporter plasmid pFPV27 or the M. smegmatis probable carotenoid promoter upstream of gfp ( pCar ) at pH 7.0, 6.0 or 5.5.

    Article Snippet: Isolated colonies of mycobacteria were patched onto 7H10 agar media (Difco) adjusted to pH 5.5 or 6.0 with HCl, or pH 7.0 with NaOH and containing 10% ADC (bovine serum albumin, dextrose and NaCl) and 0.2% glycerol and were incubated for 72 hours at 37°C in the dark.

    Techniques: Fluorescence, Activity Assay, Plasmid Preparation