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high content laser based spinning disk confocal microscope  (Revvity)


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    Revvity high content laser based spinning disk confocal microscope
    High Content Laser Based Spinning Disk Confocal Microscope, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 2279 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/opera+phenix+confocal+spinning+disk+high+content+screening+microscope/pmc13022406-282-26-35?v=Revvity
    Average 96 stars, based on 2279 article reviews
    high content laser based spinning disk confocal microscope - by Bioz Stars, 2026-08
    96/100 stars

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    Revvity opera phenix spinning disk confocal microscope
    Morphology of renal structures in kidney organoids generated with the original APEL/air-medium interface protocol. Representative immunofluorescence images of the maturing glomerular structures, stained for nephrin, and maturing tubular structures, stained for epithelial cadherin (ECAD) in healthy-donor iPSC lines HEL24.3 and HEL61.2, and the GRACILE iPSC line HEL124.2, images acquired with (A) widefield fluorescence microscopy, scale bar 500µm, and (B) the Opera Phenix spinning disk confocal <t>microscope,</t> scale bar 200µm.
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    Morphology of renal structures in kidney organoids generated with the original APEL/air-medium interface protocol. Representative immunofluorescence images of the maturing glomerular structures, stained for nephrin, and maturing tubular structures, stained for epithelial cadherin (ECAD) in healthy-donor iPSC lines HEL24.3 and HEL61.2, and the GRACILE iPSC line HEL124.2, images acquired with (A) widefield fluorescence microscopy, scale bar 500µm, and (B) the Opera Phenix spinning disk confocal microscope, scale bar 200µm.

    Journal: bioRxiv

    Article Title: Parsing glomerular and tubular structure variability in high-throughput kidney organoid culture

    doi: 10.1101/2025.05.05.652160

    Figure Lengend Snippet: Morphology of renal structures in kidney organoids generated with the original APEL/air-medium interface protocol. Representative immunofluorescence images of the maturing glomerular structures, stained for nephrin, and maturing tubular structures, stained for epithelial cadherin (ECAD) in healthy-donor iPSC lines HEL24.3 and HEL61.2, and the GRACILE iPSC line HEL124.2, images acquired with (A) widefield fluorescence microscopy, scale bar 500µm, and (B) the Opera Phenix spinning disk confocal microscope, scale bar 200µm.

    Article Snippet: Kidney organoids were also imaged using PerkinElmer Opera Phenix spinning disk confocal microscope.

    Techniques: Generated, Immunofluorescence, Staining, Fluorescence, Microscopy