EVOS Research Roundup — W35 2026
A curated batch of independent peer-reviewed papers mentioning the EVOS M3000, EVOS M5000, EVOS M7000, EVOS S1000, CellInsight CX7 and EVOS Onstage Incubator imaging platforms. Each card is tagged by disease area and imaging technique and links to Google Scholar plus the publisher DOI or full-text source.
Search source: Google Scholar (2025–2026). Plankton & Zoom does not host paywalled content.
EVOS M5000
IP47-01 — Investigation of carcinogenic effects of polystyrene microplastic on human bladder cancer cells
— Cancer · The Journal of Urology, 2026
Evos M5000 was used to track the migratory behaviour of bladder cancer cells after manual scratching, with confocal microscopy visualising microplastic particles.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Evos M5000 was used to track the migratory behaviour of bladder cancer cells after manual scratching, with confocal microscopy visualising microplastic particles.
How did the EVOS M5000 imaging platform contribute to this discovery? The EVOS M5000 supplied the imaging environment for the migration readout: Evos M5000 was used to track the migratory behaviour of bladder cancer cells after manual scratching, with confocal microscopy visualising microplastic particles. This gave the authors a reproducible visual record of cell movement to compare across conditions.
Restoration of Cx43-ERp29 interactions rescues Amyloid-β induced gap junction deficits in human astrocytes
— Neuroscience · Cellular and Molecular Life Sciences, 2026
Live-cell dye transfer was captured under a 10× objective using the EVOS M5000 inverted microscope to assess astrocyte gap-junction communication.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Live-cell dye transfer was captured under a 10× objective using the EVOS M5000 inverted microscope to assess astrocyte gap-junction communication.
How did the EVOS M5000 imaging platform contribute to this discovery? Gap-junction communication was judged from dye-transfer images taken on the EVOS M5000. Live-cell dye transfer was captured under a 10× objective using the EVOS M5000 inverted microscope to assess astrocyte gap-junction communication. The microscope therefore provided the direct functional readout used to score rescue.
Synergistic combination of additive one- and two-photon polymerisation printing methods to fabricate 3D microstructured perfusable angiogenesis-on-a-chip
— Organoid / 3D Culture · Engineering in Life Sciences, 2026
Sprout formation and stained cells were monitored with a fluorescent microscope (EVOS M5000) during perfusable chip angiogenesis assays.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Sprout formation and stained cells were monitored with a fluorescent microscope (EVOS M5000) during perfusable chip angiogenesis assays.
How did the EVOS M5000 imaging platform contribute to this discovery? The EVOS M5000 was used to watch vessel-like sprouting in real time during the perfusable-chip assay. Sprout formation and stained cells were monitored with a fluorescent microscope (EVOS M5000) during perfusable chip angiogenesis assays. Those images formed the phenotypic evidence that the chip supported angiogenesis.
Hematopoietic stem cell-derived conditioned media induces excessive mitochondrial fission via Drp-1 to target colorectal cancer
— Cancer / Stem Cell · bioRxiv, 2025
Cells were counterstained with Hoechst and imaged on an EVOS M5000 imager; DCFDA-stained cells were imaged with the EVOS M5000 fluorescent imager for ROS readouts.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Cells were counterstained with Hoechst and imaged on an EVOS M5000 imager; DCFDA-stained cells were imaged with the EVOS M5000 fluorescent imager for ROS readouts.
How did the EVOS M5000 imaging platform contribute to this discovery? ROS and mitochondrial phenotypes were turned into quantitative image data on the EVOS M5000. Cells were counterstained with Hoechst and imaged on an EVOS M5000 imager; DCFDA-stained cells were imaged with the EVOS M5000 fluorescent imager for ROS readouts. The platform thus translated fluorescent probe signals into comparable experimental measurements.
Calcium sulfate microparticle size modification for improved alginate hydrogel fabrication and its application in 3D cell culture
— Materials / 3D Culture · Frontiers of Materials Science, 2025
An inverted optical microscope (EVOS M5000) with a 20× objective was used to image particles and hydrogel-embedded 3D cultures.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? An inverted optical microscope (EVOS M5000) with a 20× objective was used to image particles and hydrogel-embedded 3D cultures.
How did the EVOS M5000 imaging platform contribute to this discovery? The EVOS M5000 resolved hydrogel-embedded 3D cultures and microparticle morphology. An inverted optical microscope (EVOS M5000) with a 20× objective was used to image particles and hydrogel-embedded 3D cultures. This allowed the authors to relate particle size directly to the resulting cell-culture architecture.
Prolyl hydroxylase inhibitor desidustat improves stroke outcomes via enhancing efferocytosis in mice with chronic kidney disease
— Neuroscience / Renal · Experimental Neurology, 2025
Images were acquired using a fluorescence microscope EVOS M5000 Imaging System at 20× magnification and quantified with ImageJ.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Images were acquired using a fluorescence microscope EVOS M5000 Imaging System at 20× magnification and quantified with ImageJ.
How did the EVOS M5000 imaging platform contribute to this discovery? High-magnification images from the EVOS M5000 were exported for ImageJ quantification. Images were acquired using a fluorescence microscope EVOS M5000 Imaging System at 20× magnification and quantified with ImageJ. That combination gave the authors numerical data tied to the fluorescence images.
YAP1 promoter-associated noncoding RNA affects Ewing sarcoma cell tumorigenicity by regulating YAP1 expression
— Cancer · Cellular & Molecular Biology Letters, 2025
Four images per transwell were taken at 10× magnification with an Invitrogen EVOS M5000 microscope; migration was quantified with ImageJ.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Four images per transwell were taken at 10× magnification with an Invitrogen EVOS M5000 microscope; migration was quantified with ImageJ.
How did the EVOS M5000 imaging platform contribute to this discovery? The EVOS M5000 supplied the imaging environment for the migration readout: Four images per transwell were taken at 10× magnification with an Invitrogen EVOS M5000 microscope; migration was quantified with ImageJ. This gave the authors a reproducible visual record of cell movement to compare across conditions.
Expression of DNAJB1-PRKACA oncogene suppresses the differentiation potential of liver progenitor organoids towards a hepatocyte lineage
— Organoids / Cancer · Scientific Reports, 2025
Images were taken on Invitrogen’s EVOS M5000 Imaging System at 2× magnification to follow organoid differentiation and marker expression.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Images were taken on Invitrogen’s EVOS M5000 Imaging System at 2× magnification to follow organoid differentiation and marker expression.
How did the EVOS M5000 imaging platform contribute to this discovery? Organoid differentiation and marker expression were followed over time with the EVOS M5000. Images were taken on Invitrogen’s EVOS M5000 Imaging System at 2× magnification to follow organoid differentiation and marker expression. Routine brightfield and fluorescence imaging made it possible to score lineage progression non-destructively.
Ras1-independent high iron-mediated hyphal formation in Candida albicans
— Infectious Disease / Microbiology · Journal of Fungi, 2026
Hyphal length was measured with an EVOS M5000 Imaging System, and image analysis performed with the integrated EVOS M5000 software.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Hyphal length was measured with an EVOS M5000 Imaging System, and image analysis performed with the integrated EVOS M5000 software.
How did the EVOS M5000 imaging platform contribute to this discovery? The EVOS M5000 both collected the hyphal images and measured their length with its integrated software. Hyphal length was measured with an EVOS M5000 Imaging System, and image analysis performed with the integrated EVOS M5000 software. That end-to-end capture-and-analysis step gave the quantitative morphology readout.
IRP1 deficiency promotes fibroblast activation through iron dysregulation: protective modulation by H2S
— Cell Biology / Fibrosis · Molecular and Cellular Biochemistry, 2026
Adherent cells were fixed and imaged using an EVOS M5000 phase-contrast microscope (Thermo Fisher Scientific).
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Adherent cells were fixed and imaged using an EVOS M5000 phase-contrast microscope (Thermo Fisher Scientific).
How did the EVOS M5000 imaging platform contribute to this discovery? Phase-contrast imaging on the EVOS M5000 recorded adherent cell morphology without fluorescent labelling. Adherent cells were fixed and imaged using an EVOS M5000 phase-contrast microscope (Thermo Fisher Scientific). This provided a label-free view of fibroblast activation under iron dysregulation.
EVOS M7000
Hematological and mitochondrial-related alterations in the thymus and spleen of rats subjected to prolonged exposure to organic dust
— Immunology / Toxicology · Medical Immunology, 2026
Mitochondrial activity in thymus and spleen samples stained with rhodamine 6G was measured on the EVOS M7000 imaging system.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Mitochondrial activity in thymus and spleen samples stained with rhodamine 6G was measured on the EVOS M7000 imaging system.
How did the EVOS M7000 imaging platform contribute to this discovery? Mitochondrial activity in stained tissue samples was read out as fluorescence intensity on the EVOS M7000. Mitochondrial activity in thymus and spleen samples stained with rhodamine 6G was measured on the EVOS M7000 imaging system. The imager turned organ-level staining into a quantitative comparison between exposure groups.
Mitochondrial ribosomal protein S30 inhibits ferroptosis and promotes tumor progression in hepatocellular carcinoma via suppressing GPX4 ubiquitination
— Cancer · International Journal of Biological Macromolecules, 2026
Colonies were visualised and imaged using the EVOS M7000; stained cells were captured with the EVOS M7000 Imaging System.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Colonies were visualised and imaged using the EVOS M7000; stained cells were captured with the EVOS M7000 Imaging System.
How did the EVOS M7000 imaging platform contribute to this discovery? The EVOS M7000 provided the imaging data behind the reported observation. Colonies were visualised and imaged using the EVOS M7000; stained cells were captured with the EVOS M7000 Imaging System. These images were the experimental readout used to support the study's conclusion.
AI-assisted label-free monitoring of bone mineral metabolism on demineralized bone paper
— Biomaterials / AI Imaging · 2025 (PMC12272952)
Samples were imaged under an EVOS M7000 microscope to visualise staining, then treated with acetic acid for quantitative mineral analysis.
Google Scholar | PMC Full Text
Frequently asked questions about this study
What did this study find? Samples were imaged under an EVOS M7000 microscope to visualise staining, then treated with acetic acid for quantitative mineral analysis.
How did the EVOS M7000 imaging platform contribute to this discovery? Staining patterns on demineralized bone paper were first documented on the EVOS M7000. Samples were imaged under an EVOS M7000 microscope to visualise staining, then treated with acetic acid for quantitative mineral analysis. Those images were then coupled with acetic-acid treatment steps to derive quantitative mineral estimates.
The post-reproductive ovary shifts from a reproductive to an immune-like organ
— Reproductive / Immunology · Molecular Human Reproduction, 2026
Ovarian tissue imaging and follicle quantification were performed with the EVOS M7000 Imaging System.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Ovarian tissue imaging and follicle quantification were performed with the EVOS M7000 Imaging System.
How did the EVOS M7000 imaging platform contribute to this discovery? Ovarian tissue sections and follicle numbers were imaged and quantified using the EVOS M7000. Ovarian tissue imaging and follicle quantification were performed with the EVOS M7000 Imaging System. This gave a reproducible structural basis for the claim that the post-reproductive ovary becomes immune-like.
Comparative study of the cytotoxic effects of outer membrane vesicles from Proteus mirabilis and Escherichia coli on HK-2 cells
— Infectious Disease / Kidney · Pathogens, 2026
ROS levels were assessed by measuring fluorescence intensity with the EVOS M7000 live-cell imaging system.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? ROS levels were assessed by measuring fluorescence intensity with the EVOS M7000 live-cell imaging system.
How did the EVOS M7000 imaging platform contribute to this discovery? ROS and mitochondrial phenotypes were turned into quantitative image data on the EVOS M7000. ROS levels were assessed by measuring fluorescence intensity with the EVOS M7000 live-cell imaging system. The platform thus translated fluorescent probe signals into comparable experimental measurements.
Real-time monitoring of the cytotoxic effect of oxygen-sensitive fluorescent poly(styrene-maleic anhydride) nanoparticles using electrical-substrate impedance sensing
— Nanomedicine / Cytotoxicity · ACS Applied Bio Materials, 2025
Fluorescence microscopy was performed using the EVOS M7000 Imaging System to visualise fluorescent nanoparticles directly in 96-well culture plates.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Fluorescence microscopy was performed using the EVOS M7000 Imaging System to visualise fluorescent nanoparticles directly in 96-well culture plates.
How did the EVOS M7000 imaging platform contribute to this discovery? The EVOS M7000 resolved hydrogel-embedded 3D cultures and microparticle morphology. Fluorescence microscopy was performed using the EVOS M7000 Imaging System to visualise fluorescent nanoparticles directly in 96-well culture plates. This allowed the authors to relate particle size directly to the resulting cell-culture architecture.
Trametinib-mediated MEK inhibition impairs cancer cell viability and invasion in patient-derived tumour avatars of glioblastoma with extraneural metastases
— Cancer / Neuro-oncology · Biomedicine & Pharmacotherapy, 2026
Spheroid images across all wells were acquired with the EVOS M7000 Imaging System under brightfield illumination using a 4× objective.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Spheroid images across all wells were acquired with the EVOS M7000 Imaging System under brightfield illumination using a 4× objective.
How did the EVOS M7000 imaging platform contribute to this discovery? Spheroid growth and morphology across wells were tracked by brightfield imaging on the EVOS M7000. Spheroid images across all wells were acquired with the EVOS M7000 Imaging System under brightfield illumination using a 4× objective. The consistent 4× brightfield acquisition made well-to-well comparisons possible.
Immunosuppression-free electrospun macroencapsulation devices with immunoprotective features for cell transplantation therapies
— Regenerative Medicine / Transplantation · RSC Advances, 2026
Sections stained with H&E or Masson’s trichrome were imaged with the EVOS M7000 Microscope to confirm islet mass and vasculature.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Sections stained with H&E or Masson’s trichrome were imaged with the EVOS M7000 Microscope to confirm islet mass and vasculature.
How did the EVOS M7000 imaging platform contribute to this discovery? Histological sections stained with H&E and Masson’s trichrome were imaged on the EVOS M7000. Sections stained with H&E or Masson’s trichrome were imaged with the EVOS M7000 Microscope to confirm islet mass and vasculature. These images were used to confirm islet mass and device vasculature in the macroencapsulation study.
Safety assessment of an oral rabies vaccine bait for wild carnivores in a seronegative dog model
— Vaccine / Veterinary · Eurasian Journal of ..., 2025
Samples were examined under fluorescent lighting using the EVOS M7000 imaging system after FITC-labelled antibody staining.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Samples were examined under fluorescent lighting using the EVOS M7000 imaging system after FITC-labelled antibody staining.
How did the EVOS M7000 imaging platform contribute to this discovery? FITC-labelled antibody staining was examined under fluorescent lighting on the EVOS M7000. Samples were examined under fluorescent lighting using the EVOS M7000 imaging system after FITC-labelled antibody staining. This provided the visual confirmation used in the oral rabies vaccine safety assessment.
Novel far-red fluorescent theranostic probes for selective imaging and targeted therapy of BET proteins in breast cancer
— Cancer / Imaging Probes · SSRN preprint, 2025
Intracellular imaging was carried out on the EVOS M7000 imaging workstation alongside a Nikon confocal laser scanning microscope.
Google Scholar | SSRN Full Text
Frequently asked questions about this study
What did this study find? Intracellular imaging was carried out on the EVOS M7000 imaging workstation alongside a Nikon confocal laser scanning microscope.
How did the EVOS M7000 imaging platform contribute to this discovery? Intracellular distribution of far-red fluorescent probes was imaged on the EVOS M7000. Intracellular imaging was carried out on the EVOS M7000 imaging workstation alongside a Nikon confocal laser scanning microscope. The EVOS images complemented the confocal data by confirming probe localisation in cultured breast-cancer cells.
EVOS S1000
Multiplex made practical: an educational workflow using directly conjugated primary antibodies 2309766
— Immunology / Multiplex Imaging · The Journal of Immunology, 2026
The workflow combines white-light photobleaching + H2O2 to combat autofluorescence and achieves superior unmixing performance using the EVOS S1000.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? The workflow combines white-light photobleaching + H2O2 to combat autofluorescence and achieves superior unmixing performance using the EVOS S1000.
How did the EVOS S1000 imaging platform contribute to this discovery? The EVOS S1000 provided the imaging data behind the reported observation. The workflow combines white-light photobleaching + H2O2 to combat autofluorescence and achieves superior unmixing performance using the EVOS S1000. These images were the experimental readout used to support the study's conclusion.
Streamlined spatial analysis of the tumour microenvironment and associated disease states using multiplex immunohistochemistry 9329
— Spatial Proteomics / Cancer · The Journal of Immunology, 2025
The EVOS S1000 imaging system made image capture and analysis remarkably straightforward in a multiplex immunohistochemistry workflow for the tumour microenvironment.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? The EVOS S1000 imaging system made image capture and analysis remarkably straightforward in a multiplex immunohistochemistry workflow for the tumour microenvironment.
How did the EVOS S1000 imaging platform contribute to this discovery? The EVOS S1000 streamlined multiplex immunohistochemistry image capture and analysis. The EVOS S1000 imaging system made image capture and analysis remarkably straightforward in a multiplex immunohistochemistry workflow for the tumour microenvironment. Its unmixing and tile-scanning capabilities made the spatial-proteomics workflow practical for routine use.
Spatial T lymphocyte infiltration into the primary melanoma tumour associates with survival
— Cancer / Spatial Proteomics · Melanoma Research, 2026
The authors note the algorithm could be applied to expanded multiplex immunofluorescence assays using EVOS S1000 Spatial Proteomics (Thermo Fisher Scientific).
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? The authors note the algorithm could be applied to expanded multiplex immunofluorescence assays using EVOS S1000 Spatial Proteomics (Thermo Fisher Scientific).
How did the EVOS S1000 imaging platform contribute to this discovery? The EVOS S1000 streamlined multiplex immunohistochemistry image capture and analysis. The authors note the algorithm could be applied to expanded multiplex immunofluorescence assays using EVOS S1000 Spatial Proteomics (Thermo Fisher Scientific). Its unmixing and tile-scanning capabilities made the spatial-proteomics workflow practical for routine use.
EVOS M3000
Conductive polymer particle-coated hydrogels promote neurite outgrowth that is further enhanced by electrical stimulation
— Neuroscience / Biomaterials · MRS Communications, 2026
Phase-contrast images were acquired daily using an EVOS M3000 imaging system with a 10× objective to monitor cell morphology during viability and differentiation studies.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Phase-contrast images were acquired daily using an EVOS M3000 imaging system with a 10× objective to monitor cell morphology during viability and differentiation studies.
How did the EVOS M3000 imaging platform contribute to this discovery? Phase-contrast imaging on the EVOS M3000 recorded adherent cell morphology without fluorescent labelling. Phase-contrast images were acquired daily using an EVOS M3000 imaging system with a 10× objective to monitor cell morphology during viability and differentiation studies. This provided a label-free view of fibroblast activation under iron dysregulation.
Neuroprotective euglobals from Eucalyptus tereticornis Smith. leaves: quantification, network pharmacology-guided in silico analysis, and experimental validation
— Neuroscience / Natural Products · Journal of Pharmacy and Pharmacology, 2026
Fluorescence images were acquired using a green fluorescence filter with the EVOS M3000 Imaging System; fluorescence intensity was quantified with ImageJ.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Fluorescence images were acquired using a green fluorescence filter with the EVOS M3000 Imaging System; fluorescence intensity was quantified with ImageJ.
How did the EVOS M3000 imaging platform contribute to this discovery? A green-fluorescence filter on the EVOS M3000 captured the relevant fluorescent signal, with intensity quantified in ImageJ. Fluorescence images were acquired using a green fluorescence filter with the EVOS M3000 Imaging System; fluorescence intensity was quantified with ImageJ. That gave a standardised readout for the neuroprotective compound screen.
Flash Assembloids: A Rapid Biofabrication of a Platform for Modeling Early Glioblastoma Invasion at the Glioblastoma–Brain Organoid Interfaces
— Cancer / Organoids · Advanced Healthcare Materials, 2026
Fluorescence images were acquired using an EVOS M3000 microscope (Thermo Fisher) for glioblastoma–brain organoid interface modelling.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Fluorescence images were acquired using an EVOS M3000 microscope (Thermo Fisher) for glioblastoma–brain organoid interface modelling.
How did the EVOS M3000 imaging platform contribute to this discovery? Organoid differentiation and marker expression were followed over time with the EVOS M3000. Fluorescence images were acquired using an EVOS M3000 microscope (Thermo Fisher) for glioblastoma–brain organoid interface modelling. Routine brightfield and fluorescence imaging made it possible to score lineage progression non-destructively.
Mutations in severe human H5N1 cases facilitate evasion from human mucus and antivirals
— Infectious Disease / Virology · bioRxiv, 2026
Cells were stored in PBS and visualised with an EVOS M3000 Imaging autofluorescent microscope for MAL-I staining comparisons.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Cells were stored in PBS and visualised with an EVOS M3000 Imaging autofluorescent microscope for MAL-I staining comparisons.
How did the EVOS M3000 imaging platform contribute to this discovery? MAL-I staining comparisons were visualised with the EVOS M3000 autofluorescence channel. Cells were stored in PBS and visualised with an EVOS M3000 Imaging autofluorescent microscope for MAL-I staining comparisons. This produced the consistent image set used to compare viral-mutation effects on mucus binding.
Spheroid cultures reveal cancer stem cell enrichment and distinct chemotherapeutic response in triple-negative breast cancer
— Cancer · BMC Cancer, 2026
Brightfield and fluorescent images were captured using an EVOS M3000 Imaging System (ThermoFisher Scientific) under similar imaging conditions across all experimental groups.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Brightfield and fluorescent images were captured using an EVOS M3000 Imaging System (ThermoFisher Scientific) under similar imaging conditions across all experimental groups.
How did the EVOS M3000 imaging platform contribute to this discovery? The EVOS M3000 provided the imaging data behind the reported observation. Brightfield and fluorescent images were captured using an EVOS M3000 Imaging System (ThermoFisher Scientific) under similar imaging conditions across all experimental groups. These images were the experimental readout used to support the study's conclusion.
Protein Arginine Methyltransferase-5 Inhibition Induces Growth Arrest and Death in Triple-Negative Breast Cancer Cells
— Cancer / Epigenetics · Future Pharmacology, 2026
Cell imaging was performed with an EVOS M3000 microscope to follow PRMT5 inhibitor-induced growth arrest and death in triple-negative breast cancer cells.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Cell imaging was performed with an EVOS M3000 microscope to follow PRMT5 inhibitor-induced growth arrest and death in triple-negative breast cancer cells.
How did the EVOS M3000 imaging platform contribute to this discovery? Inhibitor-induced growth arrest and cell death in triple-negative breast cancer were followed by time-lapse imaging on the EVOS M3000. Cell imaging was performed with an EVOS M3000 microscope to follow PRMT5 inhibitor-induced growth arrest and death in triple-negative breast cancer cells. These images provided the phenotypic evidence for the drug response.
Organoids reveal niche-specific mechanotransduction-guided human cortical patterning and cell fate acquisition
— Neuroscience / Organoids · bioRxiv, 2026
The developing cerebral cortex organoid model used an EVOS M3000 microscope for routine brightfield and fluorescence imaging during mechanotransduction studies.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? The developing cerebral cortex organoid model used an EVOS M3000 microscope for routine brightfield and fluorescence imaging during mechanotransduction studies.
How did the EVOS M3000 imaging platform contribute to this discovery? Organoid differentiation and marker expression were followed over time with the EVOS M3000. The developing cerebral cortex organoid model used an EVOS M3000 microscope for routine brightfield and fluorescence imaging during mechanotransduction studies. Routine brightfield and fluorescence imaging made it possible to score lineage progression non-destructively.
Completion of the 5′ end of the porcine teschovirus genome reveals a functional S-segment and enables reverse genetics
— Virology / Microbiology · Journal of Virology, 2026
Virus-infected cell cultures were imaged with the EVOS M3000 Imaging System to monitor cytopathic effect and confirm reverse-genetics rescue.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Virus-infected cell cultures were imaged with the EVOS M3000 Imaging System to monitor cytopathic effect and confirm reverse-genetics rescue.
How did the EVOS M3000 imaging platform contribute to this discovery? Virus-infected cultures were monitored on the EVOS M3000 to score cytopathic effect and confirm reverse-genetics rescue. Virus-infected cell cultures were imaged with the EVOS M3000 Imaging System to monitor cytopathic effect and confirm reverse-genetics rescue. The imager gave a fast, plate-based readout of rescue success.
Analysis of senescence in pituitary tumors from different lineages and the potential role of senolytic drugs as targeted therapies
— Cancer / Senescence · Frontiers in Endocrinology, 2026
Cells were incubated for 24 hours and assessed using an EVOS M3000 fluorescence microscope following senescence-associated staining.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Cells were incubated for 24 hours and assessed using an EVOS M3000 fluorescence microscope following senescence-associated staining.
How did the EVOS M3000 imaging platform contribute to this discovery? Senescence-associated staining was assessed by fluorescence microscopy on the EVOS M3000. Cells were incubated for 24 hours and assessed using an EVOS M3000 fluorescence microscope following senescence-associated staining. This provided the visual endpoint for comparing senescent phenotypes across pituitary tumour lineages.
EVOS Onstage Incubator
Glioma-intrinsic MAPK/ERK signaling promotes immunotherapy efficacy through T cell infiltration and interferon responses
— Cancer / Immunotherapy · Nature Communications, 2026
Fluorescent images of sections after inoculation were acquired using an EVOS M7000 microscope coupled with its onstage incubator system for monitoring tumour growth over time.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? Fluorescent images of sections after inoculation were acquired using an EVOS M7000 microscope coupled with its onstage incubator system for monitoring tumour growth over time.
How did the EVOS M7000 imaging platform contribute to this discovery? The onstage incubator maintained temperature, humidity and CO₂ while the EVOS M7000 captured long-term time-lapse sequences. Fluorescent images of sections after inoculation were acquired using an EVOS M7000 microscope coupled with its onstage incubator system for monitoring tumour growth over time. That combination made it possible to follow dynamic processes without interrupting culture conditions.
Rescue and Real-time Imaging of Recombinant Coxsackievirus A9 Encoding Green Fluorescent Protein
— Virology / Live-cell Imaging · Doria (University Repository), 2026
The EVOS FL Auto Imaging System (Thermo Fisher Scientific) and the attached EVOS Onstage Incubator were used to perform real-time fluorescence imaging of recombinant Coxsackievirus A9.
Google Scholar | Full Text
Frequently asked questions about this study
What did this study find? The EVOS FL Auto Imaging System (Thermo Fisher Scientific) and the attached EVOS Onstage Incubator were used to perform real-time fluorescence imaging of recombinant Coxsackievirus A9.
How did the EVOS Onstage Incubator imaging platform contribute to this discovery? The onstage incubator maintained temperature, humidity and CO₂ while the EVOS Onstage Incubator captured long-term time-lapse sequences. The EVOS FL Auto Imaging System (Thermo Fisher Scientific) and the attached EVOS Onstage Incubator were used to perform real-time fluorescence imaging of recombinant Coxsackievirus A9. That combination made it possible to follow dynamic processes without interrupting culture conditions.
Molecular and subcellular mechanisms of vital macrophage extracellular trap formation
— Immunology / Cell Biology · Frontiers in Immunology, 2025
For live-cell imaging, an EVOS onstage incubator system (Thermofisher Scientific) was mounted on the motorized stage for maintaining temperature (37 °C), humidity (80% or higher), and CO₂ during time-lapse recordings.
Google Scholar | DOI / Full Text
Frequently asked questions about this study
What did this study find? For live-cell imaging, an EVOS onstage incubator system (Thermofisher Scientific) was mounted on the motorized stage for maintaining temperature (37 °C), humidity (80% or higher), and CO₂ during time-lapse recordings.
How did the EVOS Onstage Incubator imaging platform contribute to this discovery? The onstage incubator maintained temperature, humidity and CO₂ while the EVOS Onstage Incubator captured long-term time-lapse sequences. For live-cell imaging, an EVOS onstage incubator system (Thermofisher Scientific) was mounted on the motorized stage for maintaining temperature (37 °C), humidity (80% or higher), and CO₂ during time-lapse recordings. That combination made it possible to follow dynamic processes without interrupting culture conditions.
CellInsight CX7
Themed reviews covering recent CellInsight CX7 high-content screening literature are available on the EVOS M7000 & CellInsight CX7 Research Index.
Related Roundups & Indexes
Frequently Asked Questions
What does this roundup cover?
UK-focused, independent curation of recently Google Scholar-indexed peer-reviewed papers that name EVOS or CellInsight microscope systems in their methods.
How are papers selected?
We search Google Scholar for exact model names, filter to 2025–2026 publications, verify the microscope is named in the article text or abstract, and link to the publisher or open-access version.
Can these protocols be reproduced on other microscopes?
Yes, most brightfield, fluorescence and live-cell assays are transferable to any inverted fluorescence microscope with compatible objectives and filters.
Last updated: 2026-08-27 by Plankton & Zoom.