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black flat bottom plates  (Greiner Bio)


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    Structured Review

    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 309 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/black+flat+bottom+plates/Microplate+Ps+96+Well+F-Bottom+(Chimney/pmc13010139-44-1-10
    Average 96 stars, based on 309 article reviews
    black flat bottom plates - by Bioz Stars, 2026-11
    96/100 stars

    Images

    Related Articles

    other:

    Article Title: A general strategy to enhance aptamer affinity by suppressing dissociation through symmetric assembly
    Article Snippet: Ninety-six-well black flat-bottom plates (Cat. No. 655076) were purchased from Greiner Bio-One.

    Article Title: Biophysical Basis of Paracellular Barrier Modulation by a Pan-Claudin-Binding Molecule
    Article Snippet: BLI was performed on an Octet R8 (Sartorius) at 25°C in 96-well black flat bottom plates (Greiner) using an acquisition rate of 5 Hz averaged by 20.

    Article Title: A general strategy to enhance aptamer affinity by suppressing dissociation through symmetric assembly.
    Article Snippet: Ninety-six-well black flat-bottom plates (Cat. No. 655076) were purchased from Greiner Bio-One.

    Article Title: Multi-specific antigen binding molecules targeting HIV and methods of use
    Article Snippet: Streptavidin (SA) coated biosensors tips (Pall ForteBio, CA) were used to capture biotinylated CD3 epsilon: delta heterodimer and typical immobilization levels captured on the SA sensors were 1 nm which approximately translates to 300 ng/ml of captured protein.

    Software:

    Article Title: Cryo-EM Structures of Clostridium perfringens Enterotoxin Bound to its Human Receptor, Claudin-4
    Article Snippet: For biophysical analyses, 150 nM of CpE- His10 variants were immobilized on NiNTA (Dip and Read Sartorius) sensors and tested against 0-250 nM untagged hsCLDN-4 in BLI buffer (20 mM Tris pH 7.4, 100mM NaCl, 1% glycerol, and 0.03% DDM). .. BLI was performed at 25°C in 96-well black flat bottom plates (Greiner) using an acquisition rate of 5 Hz averaged by 20 using an Octet© R8 BLI System (FortéBio/Sartorius), with assays designed and setup using Blitz Pro 1.3 Software. ..

    Article Title: Cryo-EM structures of Clostridium perfringens enterotoxin bound to its human receptor, claudin-4.
    Article Snippet: For biophysical analyses, 150 nM of CpE-His10 variants were immobilized on NiNTA (Dip and Read Sartorius) sensors and tested against 0-250 nM untagged hsCLDN-4 in BLI buffer (20 mM Tris pH 7.4, 100mM NaCl, 1% glycerol, and 0.03% DDM). .. BLI was performed at 25 C in 96-well black flat bottom plates (Greiner) using an acquisition rate of 5 Hz averaged by 20 using an Octeta R8 BLI System (FortéBio/Sartorius), with assays designed and setup using Blitz Pro 1.3 Software. ..

    Fluorescence:

    Article Title: Fluorescent protein-based Zn 2+ sensors reveal distinct responses of aerobic and anaerobic Escherichia coli cultures to excess Zn 2+
    Article Snippet: Plasmid DNA miniprep kit was from Zymo Research. .. Fluorescence spectra were obtained on an Agilent Eclipse spectrofluorometer using quartz cuvettes (Starna cells) with 1 cm path lengths or on a Tecan Spark plate reader using 96-well black flat-bottom plates (Greiner Bio-One). ..

    Article Title: Fluorescent protein-based Zn 2+ sensors reveal distinct responses of aerobic and anaerobic Escherichia coli cultures to excess Zn 2 .
    Article Snippet: Plasmid DNA miniprep kit was from Zymo Research. .. Fluorescence spectra were obtained on an Agilent Eclipse spectrofluorometer using quartz cuvettes (Starna cells) with 1 cm path lengths or on a Tecan Spark plate reader using 96-well black flat-bottom plates (Greiner Bio-One). ..



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    Greiner Bio black flat bottom 96 well plate
    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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    96
    Greiner Bio 384 well polypropylene black flat bottom plate
    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.
    384 Well Polypropylene Black Flat Bottom Plate, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    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