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gamma irradiated glass bottom  (World Precision Instruments)


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    World Precision Instruments gamma irradiated glass bottom
    Gamma Irradiated Glass Bottom, supplied by World Precision Instruments, used in various techniques. Bioz Stars score: 96/100, based on 331 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/glass+bottom+petri+dish/100-Pack+of+FluoroDish+Cell+Culture+Dish%2C+Diameter%2C+Well%2C+Petri+Dishes/bio_rxiv__64898__2026__03__30__715467-86-9-14
    Average 96 stars, based on 331 article reviews
    gamma irradiated glass bottom - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Multiple Displacement Amplification:

    Article Title: Hypertrophic adipocytes increase extracellular vesicle-mediated lipid release and reprogram breast cancer cell metabolism
    Article Snippet: For inhibitor studies, 40 μM etomoxir (Millipore #236020) or DMSO vehicle were added to the low-serum DMEM/F12 when reseeding precultured cancer cells into tissue-culture inserts. .. To assess co-localization of breast cancer cell lipid droplets and mitochondria after coculture with adipocytes, precultured MDA-MB-231s were reseeded at 100,000 cells per glass-bottom petri dish (World Precision Instruments #FD35-100) coated with 30 μg/mL collagen type I (VWR #47747-218). .. Precultured cancer cells were then stained with 200 nM MitoView 640 (Biotium #70082) for 12 hours.

    Article Title: Large adipocytes increase vesicle-mediated lipid release and promote breast cancer malignancy.
    Article Snippet: For inhibitor studies, 40 μM etomoxir (Millipore #236020) or DMSO vehicle were added to the low-serum DMEM/F12 when reseeding precultured cancer cells into tissue-culture inserts. .. Cell Reports 45, 117061, March 24, 2026 19 Mitochondrial imaging in live breast cancer cells To assess co-localization of breast cancer cell lipid droplets and mitochondria after coculture with adipocytes, precultured MDA-MB231s were reseeded at 100,000 cells per glass-bottom Petri dish (World Precision Instruments #FD35-100) coated with 30 μg/mL collagen type I (VWR #47747-218). .. For DGAT inhibition studies, DMEM/F12 was supplemented with 40 μM iDGAT1 (PF 04620110) (Tocris #1109276-89-2) and 40 μM iDGAT2 (PF 06424439) (Tocris #1469284-79-4) or an equivalent volume of DMSO vehicle and media was exchanged every 24 h.

    Imaging:

    Article Title: Correlative all-optical quantification of mass density and mechanics of subcellular compartments with fluorescence specificity
    Article Snippet: .. The cells were subcultured in a glass- bottom Petri dish (FluoroDish, World Precision Instruments Germany GmbH) 1 day prior to the measurement, and the culture medium was exchanged to Leibovitz’s L- 15 medium without phenol red (21083027, Thermo Fisher Scientific) prior to imaging. ..

    Article Title: Correlative all-optical quantification of mass density and mechanics of subcellular compartments with fluorescence specificity
    Article Snippet: .. The cells were subcultured in a glass-bottom Petri dish (FluoroDish, World Precision Instruments Germany GmbH) 1 day prior to the measurement, and the culture medium was exchanged to Leibovitz’s L-15 medium without phenol red (21083027, Thermo Fisher Scientific) prior to imaging. ..

    Article Title: Large adipocytes increase vesicle-mediated lipid release and promote breast cancer malignancy.
    Article Snippet: For inhibitor studies, 40 μM etomoxir (Millipore #236020) or DMSO vehicle were added to the low-serum DMEM/F12 when reseeding precultured cancer cells into tissue-culture inserts. .. Cell Reports 45, 117061, March 24, 2026 19 Mitochondrial imaging in live breast cancer cells To assess co-localization of breast cancer cell lipid droplets and mitochondria after coculture with adipocytes, precultured MDA-MB231s were reseeded at 100,000 cells per glass-bottom Petri dish (World Precision Instruments #FD35-100) coated with 30 μg/mL collagen type I (VWR #47747-218). .. For DGAT inhibition studies, DMEM/F12 was supplemented with 40 μM iDGAT1 (PF 04620110) (Tocris #1109276-89-2) and 40 μM iDGAT2 (PF 06424439) (Tocris #1469284-79-4) or an equivalent volume of DMSO vehicle and media was exchanged every 24 h.



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    Image Search Results


    Sample preparation and laser irradiation of the pupal terminalia. The puparium at the abdominal tip was removed to expose the developing genitalia. The pupa was placed onto a glass-bottom petri dish through an angled hole made in a drop of solidified agarose. An infrared laser (1,480 nm) was applied through the objective lens and irradiated the target cells at a certain distance (depth) from the glass.

    Journal: G3: Genes | Genomes | Genetics

    Article Title: Heat-mediated manipulation of gene expression by IR-LEGO in the developing genitalia in Drosophila

    doi: 10.1093/g3journal/jkag035

    Figure Lengend Snippet: Sample preparation and laser irradiation of the pupal terminalia. The puparium at the abdominal tip was removed to expose the developing genitalia. The pupa was placed onto a glass-bottom petri dish through an angled hole made in a drop of solidified agarose. An infrared laser (1,480 nm) was applied through the objective lens and irradiated the target cells at a certain distance (depth) from the glass.

    Article Snippet: The puparium at the abdominal tip was removed by fine forceps at 24 ± 1 h APF or 48 ± 1 h APF and placed onto a glass-bottom petri dish (35-mm dish diameter, 14-mm glass diameter, glass thickness 0.16 to 0.19 mm; D11130H, Matsunami, Japan) through a hole made by 1,000-uL pipetman tip to a 250- to 300-μL drop of solidified 1.5% agarose ( ).

    Techniques: Sample Prep, Irradiation