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black flat bottom plates  (Greiner Bio)


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    Greiner Bio black flat bottom plates
    Black Flat Bottom Plates, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 96/100, based on 306 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/black+flat+bottom+plate/Microplate+Ps+96+Well+F-Bottom+(Chimney/pmc13010139-44-1-10
    Average 96 stars, based on 306 article reviews
    black flat bottom plates - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    other:

    Article Title: Serological and molecular analysis of henipavirus infections in synanthropic fruit bat and rodent populations in the Centre and North regions of Cameroon (2018-2020).
    Article Snippet: A volume of 0.5μL of each coated bead in 50μL bead buffer were added to appropriate wells of a black flat bottom plate (Greiner, Frickenhausen, Germany).

    Article Title: A Cdk5-derived peptide inhibits Cdk5/p25 activity and improves neurodegenerative phenotypes
    Article Snippet: Before starting the BLI experiment, the streptavidin sensors were soaked by dipping in 200 μL of assay buffer in a 96-well Greiner Bio- One Black flat bottom plate (#655209).

    Article Title: A general strategy to enhance aptamer affinity by suppressing dissociation through symmetric assembly.
    Article Snippet: All solutions (200 μl) were loaded into a 96-well black flat-bottom plate (Greiner Bio-One, Cat. No. 655076).

    Article Title: Exifone Is a Potent HDAC1 Activator with Neuroprotective Activity in Human Neuronal Models of Neurodegeneration.
    Article Snippet: Before the BLI assay, the streptavidin sensors were soaked by being dipped in 200 μL of assay buffer in a 96-well Greiner Bio-One Black flat bottom plate (#655209).

    Article Title: Hsp90α forms condensate engaging client proteins with RG motif repeats
    Article Snippet: Assays were performed at 37 °C in a 96-well black flat bottom plate (Greiner Bio-One) with orbital shaking at 1000 rpm in buffer containing 50 mM Tris, pH 7.5 and 100 mM NaCl.

    Article Title: Design of Ig-like binders targeting α-synuclein fibril for mitigating its pathological activities
    Article Snippet: 200 μL α-syn/α-syn 100 /K19/K19-α-syn 101-140 monomers/PFF or buffer (50 mM Na 2 HPO 4 -NaH 2 PO 4 , pH 7.0, 50 mM NaCl, 0.05% Tween-20) were plated in a 96-well black flat bottom plate (Greiner Bio-One, 655209).

    Article Title: A general strategy to enhance aptamer affinity by suppressing dissociation through symmetric assembly
    Article Snippet: All solutions (200 μl) were loaded into a 96-well black flat-bottom plate (Greiner Bio-One, Cat. No. 655076).

    Article Title: Nuclease-assisted selection of slow-off rate aptamers
    Article Snippet: Two hundred microliters of these solutions was loaded into the wells of a 96-well black flat bottom plate (Greiner).



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    Comparison of target strain growth in monoculture and co-culture conditions. (A, B) Relative fluorescence units (RFU) over time for target strains OfT6-21 with pBU164 (A) and McT4-56 with pBU164 (B) cultured in GASW-Tris broth in <t>a</t> <t>96-well</t> microtiter plate. Each target strain was grown in monoculture (purple line with circles), in co-culture with its respective wildtype (WT) strain (blue line with diamonds), and in co-culture with the putative coral probiotic, Pseudoalteromonas sp. strain McH1-7 (green line with triangles) ( n = 10 per treatment). (B) Area under the curve (AUC) calculations for target strain OfT6-21 with pBU164 show significant differences in growth between the monoculture (purple circles), co-culture with its WT strain (blue diamonds), and co-culture with strain McH1-7 (green triangles) (one-way ANOVA; F(2, 27) = 37.90, p < 0.0001 , n = 10 per group). (D) AUC calculations for target strain McT4-56 with pBU164 show significant differences in growth across monoculture (purple circles), co-culture with its WT strain (blue diamonds), and co-culture with strain McH1-7 (green triangles) (one-way ANOVA; F(2, 27) = 316.2, p < 0.0001 , n = 10 per group). Asterisks indicate statistical significance (****= p ≤ 0.0001 ). Error bars represent the standard error of the mean (SEM), and bar height in the bar graphs represent the mean.
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    Comparison of target strain growth in monoculture and co-culture conditions. (A, B) Relative fluorescence units (RFU) over time for target strains OfT6-21 with pBU164 (A) and McT4-56 with pBU164 (B) cultured in GASW-Tris broth in a 96-well microtiter plate. Each target strain was grown in monoculture (purple line with circles), in co-culture with its respective wildtype (WT) strain (blue line with diamonds), and in co-culture with the putative coral probiotic, Pseudoalteromonas sp. strain McH1-7 (green line with triangles) ( n = 10 per treatment). (B) Area under the curve (AUC) calculations for target strain OfT6-21 with pBU164 show significant differences in growth between the monoculture (purple circles), co-culture with its WT strain (blue diamonds), and co-culture with strain McH1-7 (green triangles) (one-way ANOVA; F(2, 27) = 37.90, p < 0.0001 , n = 10 per group). (D) AUC calculations for target strain McT4-56 with pBU164 show significant differences in growth across monoculture (purple circles), co-culture with its WT strain (blue diamonds), and co-culture with strain McH1-7 (green triangles) (one-way ANOVA; F(2, 27) = 316.2, p < 0.0001 , n = 10 per group). Asterisks indicate statistical significance (****= p ≤ 0.0001 ). Error bars represent the standard error of the mean (SEM), and bar height in the bar graphs represent the mean.

    Journal: bioRxiv

    Article Title: Building the Marine Probiotic Platform: Developing a High-Throughput Process to Discover Coral Probiotics for Stony Coral Tissue Loss Disease

    doi: 10.64898/2026.01.11.698879

    Figure Lengend Snippet: Comparison of target strain growth in monoculture and co-culture conditions. (A, B) Relative fluorescence units (RFU) over time for target strains OfT6-21 with pBU164 (A) and McT4-56 with pBU164 (B) cultured in GASW-Tris broth in a 96-well microtiter plate. Each target strain was grown in monoculture (purple line with circles), in co-culture with its respective wildtype (WT) strain (blue line with diamonds), and in co-culture with the putative coral probiotic, Pseudoalteromonas sp. strain McH1-7 (green line with triangles) ( n = 10 per treatment). (B) Area under the curve (AUC) calculations for target strain OfT6-21 with pBU164 show significant differences in growth between the monoculture (purple circles), co-culture with its WT strain (blue diamonds), and co-culture with strain McH1-7 (green triangles) (one-way ANOVA; F(2, 27) = 37.90, p < 0.0001 , n = 10 per group). (D) AUC calculations for target strain McT4-56 with pBU164 show significant differences in growth across monoculture (purple circles), co-culture with its WT strain (blue diamonds), and co-culture with strain McH1-7 (green triangles) (one-way ANOVA; F(2, 27) = 316.2, p < 0.0001 , n = 10 per group). Asterisks indicate statistical significance (****= p ≤ 0.0001 ). Error bars represent the standard error of the mean (SEM), and bar height in the bar graphs represent the mean.

    Article Snippet: To screen for antibacterial activity against the target strains, each tester culture (coral mucus isolate) was co-cultured with each target strain separately in a sterile black flat bottom 96-well plate (Cell culture microplate, PS, F-bottom, 655086, Greiner Bio-One).

    Techniques: Comparison, Co-Culture Assay, Fluorescence, Cell Culture