macconkey agar Search Results


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  • 99
    Thermo Fisher macconkey agar
    Colony of S. flexneri on commercial <t>MaCconkey</t> agar (Oxoid) (A) and MaCconkey agar was made from defatted brebra flour as peptone substitute (B).
    Macconkey Agar, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1778 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/macconkey agar/product/Thermo Fisher
    Average 99 stars, based on 1778 article reviews
    Price from $9.99 to $1999.99
    macconkey agar - by Bioz Stars, 2020-05
    99/100 stars
      Buy from Supplier

    96
    Millipore macconkey agar
    Number of SNPs identified via WGS. <t>MacConkey</t> agar isolates from patient/donor pair 9 underwent WGS and core genome alignment analysis with Parsnp. Data are ordered according to their similarity with donor isolate 5D. Murine clbB + isolate NC101 is shown for comparison. D, donor isolates; P, patient isolates. Five donor (D) and 5 patient post-FMT (P) isolates are shown. Five isolates from the patient pre-FMT were also sequenced but were too divergent to be aligned alongside the E . coli isolates, as the pre-FMT isolates were all Klebsiella or Morganella species.
    Macconkey Agar, supplied by Millipore, used in various techniques. Bioz Stars score: 96/100, based on 287 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/macconkey agar/product/Millipore
    Average 96 stars, based on 287 article reviews
    Price from $9.99 to $1999.99
    macconkey agar - by Bioz Stars, 2020-05
    96/100 stars
      Buy from Supplier

    94
    Thermo Fisher macconkey
    Number of SNPs identified via WGS. <t>MacConkey</t> agar isolates from patient/donor pair 9 underwent WGS and core genome alignment analysis with Parsnp. Data are ordered according to their similarity with donor isolate 5D. Murine clbB + isolate NC101 is shown for comparison. D, donor isolates; P, patient isolates. Five donor (D) and 5 patient post-FMT (P) isolates are shown. Five isolates from the patient pre-FMT were also sequenced but were too divergent to be aligned alongside the E . coli isolates, as the pre-FMT isolates were all Klebsiella or Morganella species.
    Macconkey, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 214 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/macconkey/product/Thermo Fisher
    Average 94 stars, based on 214 article reviews
    Price from $9.99 to $1999.99
    macconkey - by Bioz Stars, 2020-05
    94/100 stars
      Buy from Supplier

    Image Search Results


    Colony of S. flexneri on commercial MaCconkey agar (Oxoid) (A) and MaCconkey agar was made from defatted brebra flour as peptone substitute (B).

    Journal: Asian Pacific Journal of Tropical Biomedicine

    Article Title: Production of microbial medium from defatted brebra (Milletia ferruginea) seed flour to substitute commercial peptone agar

    doi: 10.1016/S2221-1691(13)60157-4

    Figure Lengend Snippet: Colony of S. flexneri on commercial MaCconkey agar (Oxoid) (A) and MaCconkey agar was made from defatted brebra flour as peptone substitute (B).

    Article Snippet: The colony colour and other morphological qualities of S. flexneri grown on commercial MaCconkey agar (Oxoid) (A) and MaCconkey agar was made from defatted brebra flour as peptone substitute (B) ( ).

    Techniques:

    Schematic representation of the working protocol. A total of 1,100 saline fecal suspensions were cultured in both MacConkey plates supplemented with 4 μg/ml of ceftazidime (MCK-CAZ) and Luria-Bertani broth with 1 μg/ml of imipenem (LB-IMP).

    Journal: Journal of Clinical Microbiology

    Article Title: Fecal Carriage of Carbapenemase-Producing Enterobacteriaceae: a Hidden Reservoir in Hospitalized and Nonhospitalized Patients

    doi: 10.1128/JCM.00020-12

    Figure Lengend Snippet: Schematic representation of the working protocol. A total of 1,100 saline fecal suspensions were cultured in both MacConkey plates supplemented with 4 μg/ml of ceftazidime (MCK-CAZ) and Luria-Bertani broth with 1 μg/ml of imipenem (LB-IMP).

    Article Snippet: Briefly, 100 μl of saline fecal suspension (one full planting loop in 3 ml of saline) was cultured either in 2 ml tubes of Luria-Bertani broth (Pronadisa, Madrid, Spain) supplemented with imipenem (1 μg/ml) or in MacConkey agar plates (Oxoid Ltd., Basingstoke, England) supplemented with ceftazidime (4 μg/ml).

    Techniques: Cell Culture

    Culture characteristics of bacterial isolates on different media. A) Escherichia coli on MacConkey’s agar, B) Bacillus cereus on MacConkey’s agar, C) Salmonella typhi on Salmonella shigella agar, and D) Pseudomonas aeruginosa on Salmonella shigella agar.

    Journal: Saudi Medical Journal

    Article Title: Occurrence and antibacterial susceptibility pattern of bacterial pathogens isolated from diarrheal patients in Pakistan

    doi: 10.15537/smj.2016.3.14449

    Figure Lengend Snippet: Culture characteristics of bacterial isolates on different media. A) Escherichia coli on MacConkey’s agar, B) Bacillus cereus on MacConkey’s agar, C) Salmonella typhi on Salmonella shigella agar, and D) Pseudomonas aeruginosa on Salmonella shigella agar.

    Article Snippet: For purification, the different colonies from initial growth were streaked on MacConkey’s agar (Oxoid, UK) and Salmonella shigella agar (Oxoid, UK) plates, and incubated at 37°C for 24 hours.

    Techniques:

    Activation of NF-κB in HEK-Blue hTLR4 cells by B . pseudomallei K96243 cultured in different media. HEK-Blue hTLR4 cells were stimulated with heat-killed B . pseudomallei K96243 at 10 6 or 10 7 CFU/ml at 37°C in 5% CO 2 for 24 h. NF-κB activation was determined in the supernatant by a SEAP reporter assay with HEK-Blue detection. Mean ± SD of three independent experiment were illustrated. TSA; trypticase soy agar, LB; Luria-Bertani agar, Ash; Ashdown agar, BA; Blood agar, Mac; MacConkey agar, M9; M9 minimal medium agar.

    Journal: PLoS Neglected Tropical Diseases

    Article Title: Comprehensive analysis of clinical Burkholderia pseudomallei isolates demonstrates conservation of unique lipid A structure and TLR4-dependent innate immune activation

    doi: 10.1371/journal.pntd.0006287

    Figure Lengend Snippet: Activation of NF-κB in HEK-Blue hTLR4 cells by B . pseudomallei K96243 cultured in different media. HEK-Blue hTLR4 cells were stimulated with heat-killed B . pseudomallei K96243 at 10 6 or 10 7 CFU/ml at 37°C in 5% CO 2 for 24 h. NF-κB activation was determined in the supernatant by a SEAP reporter assay with HEK-Blue detection. Mean ± SD of three independent experiment were illustrated. TSA; trypticase soy agar, LB; Luria-Bertani agar, Ash; Ashdown agar, BA; Blood agar, Mac; MacConkey agar, M9; M9 minimal medium agar.

    Article Snippet: The bacteria were cultured on TSA (Oxoid, Hants, UK) for 16–18 h. Approximately 10 colonies were streaked onto agar plates and incubated for 16–18 h under one of the following conditions: (i) TSA (pH 7.4) at 25 o C, (ii) TSA (pH 7.4) at 37 o C, (iii) TSA (pH 7.4) at 42 o C, (iv) TSA (pH 4.5) at 37 o C, (v) TSA (pH 8.5) at 37 o C, (vi) TSA (pH 7.4) plus 2 mM H2 O2 (Merck, Darmstadt, Germany) at 37 o C, (vii) TSA (pH 7.4) plus 5 mM H2 O2 at 37 o C, (viii) TSA (pH 7.4) plus 50 mM NaNO2 (Sigma-Aldrich, MO, USA) at 37 o C, (ix) TSA (pH 7.4) plus 100 mM NaNO2 at 37 o C, (x) TSA (pH 7.4) plus 1 mM MgCl2 (Fisher Scientific, Leics, UK) at 37 o C, (xi) TSA (pH 7.4) plus 8 μM MgCl2 at 37 o C, (xii) Luria-Bertani agar (LB) (BD, MD, USA) (pH 7.4) at 37 o C, (xiii) Ashdown agar (pH 7.4) at 37 o C, (xiv) blood agar (Oxoid, Hants, UK) (pH 7.4) at 37 o C, (xv) MacConkey agar (Oxoid, Hants, UK) (pH 7.4) at 37 o C, and (xvi) M9 minimal medium agar (Sigma-Aldrich, MO, USA) (pH 7.4) at 37 o C. The bacteria were harvested using a 10 μl loop and further extracted for lipid A.

    Techniques: Activation Assay, Cell Culture, Reporter Assay

    Number of SNPs identified via WGS. MacConkey agar isolates from patient/donor pair 9 underwent WGS and core genome alignment analysis with Parsnp. Data are ordered according to their similarity with donor isolate 5D. Murine clbB + isolate NC101 is shown for comparison. D, donor isolates; P, patient isolates. Five donor (D) and 5 patient post-FMT (P) isolates are shown. Five isolates from the patient pre-FMT were also sequenced but were too divergent to be aligned alongside the E . coli isolates, as the pre-FMT isolates were all Klebsiella or Morganella species.

    Journal: JCI Insight

    Article Title: Transmission and clearance of potential procarcinogenic bacteria during fecal microbiota transplantation for recurrent Clostridioides difficile

    doi: 10.1172/jci.insight.130848

    Figure Lengend Snippet: Number of SNPs identified via WGS. MacConkey agar isolates from patient/donor pair 9 underwent WGS and core genome alignment analysis with Parsnp. Data are ordered according to their similarity with donor isolate 5D. Murine clbB + isolate NC101 is shown for comparison. D, donor isolates; P, patient isolates. Five donor (D) and 5 patient post-FMT (P) isolates are shown. Five isolates from the patient pre-FMT were also sequenced but were too divergent to be aligned alongside the E . coli isolates, as the pre-FMT isolates were all Klebsiella or Morganella species.

    Article Snippet: Amplified cultures were then plated onto the following selective plates for an additional 24–48 hours: Fusobacterium Selective Agar (FSA, Anaerobe Systems) for F . nucleatum , Bacteroides Bile Esculin Agar (BBE, Anaerobe Systems) for B . fragilis , and MacConkey Agar (MilliporeSigma) for E . coli .

    Techniques:

    The microbial count in water samples, expressed as Log 10 (CFU/mL). The microbial count was carried out in plate count agar (PCA) media (black bars) and MacConkey (MC) media (gray bars) after incubation at 20°C for 48 h in the absence of antibiotics (A) , and with the addition of antibiotics at a final concentration of 20 μg/mL. Frequency of the antibiotic-resistant colonies (B) was calculated as the ratio of the colony growth in the presence of a specific antibiotic compared to colony growth in its absence. Numbers are expressed as the percentage ± the standard deviation.

    Journal: Frontiers in Microbiology

    Article Title: Viromes As Genetic Reservoir for the Microbial Communities in Aquatic Environments: A Focus on Antimicrobial-Resistance Genes

    doi: 10.3389/fmicb.2017.01095

    Figure Lengend Snippet: The microbial count in water samples, expressed as Log 10 (CFU/mL). The microbial count was carried out in plate count agar (PCA) media (black bars) and MacConkey (MC) media (gray bars) after incubation at 20°C for 48 h in the absence of antibiotics (A) , and with the addition of antibiotics at a final concentration of 20 μg/mL. Frequency of the antibiotic-resistant colonies (B) was calculated as the ratio of the colony growth in the presence of a specific antibiotic compared to colony growth in its absence. Numbers are expressed as the percentage ± the standard deviation.

    Article Snippet: Evaluation of Antibiotic Resistant Colony Frequencies For the evaluation of antibiotic resistant colony frequencies, samples from the 0.2 μm TFF system retentate (see next paragraph) were used for dilution and plating on two selective media: plate count agar (PCA) and MacConkey (MC) agar (Sigma–Aldrich).

    Techniques: Incubation, Concentration Assay, Standard Deviation