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solid agar medium middlebrook 7h10  (MiddleBrook Pharmaceuticals)

 
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    MiddleBrook Pharmaceuticals solid agar medium middlebrook 7h10
    Solid Agar Medium Middlebrook 7h10, supplied by MiddleBrook Pharmaceuticals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/solid+agar+medium+middlebrook+7h10/middlebrook+7h9+broth/pm40237045-295-19-19
    Average 90 stars, based on 1 article reviews
    solid agar medium middlebrook 7h10 - by Bioz Stars, 2026-09
    90/100 stars

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    a) PIM, LM, and LAM biosynthesis pathway. Bold text, enzymes. b) Lipoglycans extracted from WT and Δ mptA cells, visualized by glycan staining. c) Comparison of colony size between WT and Δ mptA on Middlebrook <t>7H10</t> and LB solid agar media grown at 30°C or 37°C. Top: quantification of colony area for each condition; bottom: example images of WT and Δ mptA colonies grown in each condition. d) Cross-sectional view of live/dead imaging of microcolonies from WT and Δ mptA strains stained with SYTO9 (live) and propidium iodide (dead) grown as micro-aggregates in LB medium.
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    a) PIM, LM, and LAM biosynthesis pathway. Bold text, enzymes. b) Lipoglycans extracted from WT and Δ mptA cells, visualized by glycan staining. c) Comparison of colony size between WT and Δ mptA on Middlebrook <t>7H10</t> and LB solid agar media grown at 30°C or 37°C. Top: quantification of colony area for each condition; bottom: example images of WT and Δ mptA colonies grown in each condition. d) Cross-sectional view of live/dead imaging of microcolonies from WT and Δ mptA strains stained with SYTO9 (live) and propidium iodide (dead) grown as micro-aggregates in LB medium.
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    a) PIM, LM, and LAM biosynthesis pathway. Bold text, enzymes. b) Lipoglycans extracted from WT and Δ mptA cells, visualized by glycan staining. c) Comparison of colony size between WT and Δ mptA on Middlebrook <t>7H10</t> and LB solid agar media grown at 30°C or 37°C. Top: quantification of colony area for each condition; bottom: example images of WT and Δ mptA colonies grown in each condition. d) Cross-sectional view of live/dead imaging of microcolonies from WT and Δ mptA strains stained with SYTO9 (live) and propidium iodide (dead) grown as micro-aggregates in LB medium.
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    a) PIM, LM, and LAM biosynthesis pathway. Bold text, enzymes. b) Lipoglycans extracted from WT and Δ mptA cells, visualized by glycan staining. c) Comparison of colony size between WT and Δ mptA on Middlebrook <t>7H10</t> and LB solid agar media grown at 30°C or 37°C. Top: quantification of colony area for each condition; bottom: example images of WT and Δ mptA colonies grown in each condition. d) Cross-sectional view of live/dead imaging of microcolonies from WT and Δ mptA strains stained with SYTO9 (live) and propidium iodide (dead) grown as micro-aggregates in LB medium.
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    Image Search Results


    a) PIM, LM, and LAM biosynthesis pathway. Bold text, enzymes. b) Lipoglycans extracted from WT and Δ mptA cells, visualized by glycan staining. c) Comparison of colony size between WT and Δ mptA on Middlebrook 7H10 and LB solid agar media grown at 30°C or 37°C. Top: quantification of colony area for each condition; bottom: example images of WT and Δ mptA colonies grown in each condition. d) Cross-sectional view of live/dead imaging of microcolonies from WT and Δ mptA strains stained with SYTO9 (live) and propidium iodide (dead) grown as micro-aggregates in LB medium.

    Journal: bioRxiv

    Article Title: Lipoarabinomannan regulates septation in Mycobacterium smegmatis

    doi: 10.1101/2023.03.26.534150

    Figure Lengend Snippet: a) PIM, LM, and LAM biosynthesis pathway. Bold text, enzymes. b) Lipoglycans extracted from WT and Δ mptA cells, visualized by glycan staining. c) Comparison of colony size between WT and Δ mptA on Middlebrook 7H10 and LB solid agar media grown at 30°C or 37°C. Top: quantification of colony area for each condition; bottom: example images of WT and Δ mptA colonies grown in each condition. d) Cross-sectional view of live/dead imaging of microcolonies from WT and Δ mptA strains stained with SYTO9 (live) and propidium iodide (dead) grown as micro-aggregates in LB medium.

    Article Snippet: For colony growth, serial dilutions of planktonic culture were spread evenly over LB or Middlebrook 7H10 (supplemented with 15 mM NaCl and 0.2% (w/v) glucose) solid agar medium and incubated at 30°C or 37°C for 3 – 4 days.

    Techniques: Glycoproteomics, Staining, Comparison, Imaging