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Sarstedt flat bottom 96 well plate
Flat Bottom 96 Well Plate, supplied by Sarstedt, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/flat+bottom+96+well+plates/96+plate+well/pm42128178-93-32-35
Average 86 stars, based on 1 article reviews
flat bottom 96 well plate - by Bioz Stars, 2026-10
86/100 stars

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96 Well Plates:

Article Title: Elucidation of Molecular Mechanisms of Lipid-Altered Cytotoxicity of TDP-43 Fibrils
Article Snippet: .. Cells were seeded at a density of 20,000 cells per well in flat-bottom 96-well plates (83.3924.300, Sarstedt, Germany) and incubated for 24 h. Following a 24 h treatment with protein samples, cells were collected, centrifuged at 400 g for 5 min, and resuspended in PBS. .. JC-1 dye from the MitoProbe JC-1 Assay Kit (Thermo Fisher Scientific, cat. no. M34152A) was applied at 2.0 μg/mL, and cells were incubated for 30 min at 37 °C.

Article Title: NLRP3 activators disrupt the endocytic AP2 complex and plasma membrane signaling
Article Snippet: .. Briefly, stable SNAP-β 2 AR HEK293 cells( ) were seeded into pDL-coated, white, flat bottom 96-well plates (Sarstedt, order-No. 82.1581.210) at 50000 cells per well and cultivated for 24 hours at 37 °C and 5 % CO 2 . .. Cells were labelled with 50 μl of 100 nM SNAP-Lumi4-Tb (Revvity, #SSNPTBC) in HBSS supplemented with 20 mM HEPES for one hour at 37 °C.

Article Title: TopBP1 biomolecular condensates as a new therapeutic target in advanced-stage colorectal cancer
Article Snippet: .. Cells were seeded at 500 cells/well in black flat-bottom 96-well plates (Sarstedt, #83.3924), cultured for 24 hr, then incubated with AZD2858 and/or FOLFIRI for 96 hr. .. Then, PI (Sigma, #P4864) and Hoechst 33342 (Thermo Fisher Scientific, #62249) were added to the plates at the final concentrations of 1 and 5 μg/mL, respectively.

Article Title: Mechanistic Insights on Surface Adsorption of Rice-based Biomolecules on Stainless Steel 316L and its Effects on Corrosion and Metal Migration
Article Snippet: Austenitic stainless steel (AISI 316L) is the dominant material in food processing equipment due to high corrosion resistance and mechanical durability.. The shift from animal-to plant-based food processing introduces new challenges for material performance, as plant-derived biomolecules may interact differently with foodcontact surfaces than animal proteins.. These interactions can modify interfacial properties, with consequences for fouling, corrosion, and metal migration.

Incubation:

Article Title: Elucidation of Molecular Mechanisms of Lipid-Altered Cytotoxicity of TDP-43 Fibrils
Article Snippet: .. Cells were seeded at a density of 20,000 cells per well in flat-bottom 96-well plates (83.3924.300, Sarstedt, Germany) and incubated for 24 h. Following a 24 h treatment with protein samples, cells were collected, centrifuged at 400 g for 5 min, and resuspended in PBS. .. JC-1 dye from the MitoProbe JC-1 Assay Kit (Thermo Fisher Scientific, cat. no. M34152A) was applied at 2.0 μg/mL, and cells were incubated for 30 min at 37 °C.

Article Title: Elucidation of Molecular Mechanisms of Lipid-Altered Cytotoxicity of TDP-43 Fibrils.
Article Snippet: .. Cells were seeded at a density of 20,000 cells per well in flat-bottom 96-well plates (83.3924.300, Sarstedt, Germany) and incubated for 24 h. Following a 24 h treatment with protein samples, cells were collected, centrifuged at 400g for 5 min, and resuspended in PBS. .. Cells were seeded at a density of 20,000 cells per well in flat-bottom 96-well plates (83.3924.300, Sarstedt, Germany) and incubated for 24 h. Following a 24 h treatment with protein samples, cells were collected, centrifuged at 400g for 5 min, and resuspended in PBS.

Article Title: TopBP1 biomolecular condensates as a new therapeutic target in advanced-stage colorectal cancer
Article Snippet: .. Cells were seeded at 500 cells/well in black flat-bottom 96-well plates (Sarstedt, #83.3924), cultured for 24 hr, then incubated with AZD2858 and/or FOLFIRI for 96 hr. .. Then, PI (Sigma, #P4864) and Hoechst 33342 (Thermo Fisher Scientific, #62249) were added to the plates at the final concentrations of 1 and 5 μg/mL, respectively.

Suspension:

Article Title: Paving the way or sharing goods?—Interactions between pairs of Staphylococcus aureus and Pseudomonas aeruginosa sequentially isolated from respiratory samples of patients on mechanical ventilation
Article Snippet: .. Thereafter, the suspensions were diluted to OD 600 = 0.1, and from this suspension 20 μL were added to 180 μL pure media in flat-bottom 96-well plates (standard non-coated microplates, Sarstedt). ..

Cell Culture:

Article Title: TopBP1 biomolecular condensates as a new therapeutic target in advanced-stage colorectal cancer
Article Snippet: .. Cells were seeded at 500 cells/well in black flat-bottom 96-well plates (Sarstedt, #83.3924), cultured for 24 hr, then incubated with AZD2858 and/or FOLFIRI for 96 hr. .. Then, PI (Sigma, #P4864) and Hoechst 33342 (Thermo Fisher Scientific, #62249) were added to the plates at the final concentrations of 1 and 5 μg/mL, respectively.

Concentration Assay:

Article Title: Mechanistic Insights on Surface Adsorption of Rice-based Biomolecules on Stainless Steel 316L and its Effects on Corrosion and Metal Migration
Article Snippet: Austenitic stainless steel (AISI 316L) is the dominant material in food processing equipment due to high corrosion resistance and mechanical durability.. The shift from animal-to plant-based food processing introduces new challenges for material performance, as plant-derived biomolecules may interact differently with foodcontact surfaces than animal proteins.. These interactions can modify interfacial properties, with consequences for fouling, corrosion, and metal migration.



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Relative biofilm formation by monocultures and cocultures in the three media: (A) M1, (B) M2, and (C) M3. Biofilm formation was assessed by the crystal violet assay and the biofilm volume normalized to that of the reference stain Pa01 in each medium. The bars represent an average of 12 culture wells <t>in</t> <t>96-well</t> plates from two different biological replica performed on different days. Error bars represent standard deviation. *Represent significantly different values ( p < 0.01, Students t -test) between monoculture and coculture. Blue bars represent P. aeruginosa ( Pa ) and red bars S. aureus ( Sa ), crossed bars cocultures.
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Relative biofilm formation by monocultures and cocultures in the three media: (A) M1, (B) M2, and (C) M3. Biofilm formation was assessed by the crystal violet assay and the biofilm volume normalized to that of the reference stain Pa01 in each medium. The bars represent an average of 12 culture wells <t>in</t> <t>96-well</t> plates from two different biological replica performed on different days. Error bars represent standard deviation. *Represent significantly different values ( p < 0.01, Students t -test) between monoculture and coculture. Blue bars represent P. aeruginosa ( Pa ) and red bars S. aureus ( Sa ), crossed bars cocultures.
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Relative biofilm formation by monocultures and cocultures in the three media: (A) M1, (B) M2, and (C) M3. Biofilm formation was assessed by the crystal violet assay and the biofilm volume normalized to that of the reference stain Pa01 in each medium. The bars represent an average of 12 culture wells <t>in</t> <t>96-well</t> plates from two different biological replica performed on different days. Error bars represent standard deviation. *Represent significantly different values ( p < 0.01, Students t -test) between monoculture and coculture. Blue bars represent P. aeruginosa ( Pa ) and red bars S. aureus ( Sa ), crossed bars cocultures.
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Relative biofilm formation by monocultures and cocultures in the three media: (A) M1, (B) M2, and (C) M3. Biofilm formation was assessed by the crystal violet assay and the biofilm volume normalized to that of the reference stain Pa01 in each medium. The bars represent an average of 12 culture wells <t>in</t> <t>96-well</t> plates from two different biological replica performed on different days. Error bars represent standard deviation. *Represent significantly different values ( p < 0.01, Students t -test) between monoculture and coculture. Blue bars represent P. aeruginosa ( Pa ) and red bars S. aureus ( Sa ), crossed bars cocultures.
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Image Search Results


Relative biofilm formation by monocultures and cocultures in the three media: (A) M1, (B) M2, and (C) M3. Biofilm formation was assessed by the crystal violet assay and the biofilm volume normalized to that of the reference stain Pa01 in each medium. The bars represent an average of 12 culture wells in 96-well plates from two different biological replica performed on different days. Error bars represent standard deviation. *Represent significantly different values ( p < 0.01, Students t -test) between monoculture and coculture. Blue bars represent P. aeruginosa ( Pa ) and red bars S. aureus ( Sa ), crossed bars cocultures.

Journal: Frontiers in Microbiology

Article Title: Paving the way or sharing goods?—Interactions between pairs of Staphylococcus aureus and Pseudomonas aeruginosa sequentially isolated from respiratory samples of patients on mechanical ventilation

doi: 10.3389/fmicb.2026.1798383

Figure Lengend Snippet: Relative biofilm formation by monocultures and cocultures in the three media: (A) M1, (B) M2, and (C) M3. Biofilm formation was assessed by the crystal violet assay and the biofilm volume normalized to that of the reference stain Pa01 in each medium. The bars represent an average of 12 culture wells in 96-well plates from two different biological replica performed on different days. Error bars represent standard deviation. *Represent significantly different values ( p < 0.01, Students t -test) between monoculture and coculture. Blue bars represent P. aeruginosa ( Pa ) and red bars S. aureus ( Sa ), crossed bars cocultures.

Article Snippet: Thereafter, the suspensions were diluted to OD 600 = 0.1, and from this suspension 20 μL were added to 180 μL pure media in flat-bottom 96-well plates (standard non-coated microplates, Sarstedt).

Techniques: Crystal Violet Assay, Staining, Standard Deviation