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Eclipse a1r microscope

Manufactured by Nikon
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Sourced in United States

The Eclipse A1R microscope is a high-performance confocal microscope designed for advanced imaging applications. It features a fast and sensitive laser scanning system, enabling real-time 3D imaging and high-resolution visualization of samples. The Eclipse A1R provides researchers with a robust and versatile platform for a wide range of microscopy techniques.

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Lab products found in correlation

Nis elements software, by Nikon (1 mentions) Nis element software, by Nikon (1 mentions)

Close spelling variants of this product

A1R Eclipse Ti microscope Eclipse Ti A1R-A1 confocal microscope A1R MP ECLIPSE Ti confocal microscope Nikon A1R Eclipse Ti confocal microscope A1R microscope Eclipse microscope

2 protocols using eclipse a1r microscope

1

Quantify Mitochondrial Dynamics in Cells

Cited 1 time
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To quantify donor mitochondria internalization, fusion with host mitochondria, and mitophagy of donor and host mitochondria (per colocalization with lysosomes), stained CM were co-incubated with pHrodo Red-stained donor mitochondria. 3–10 cells/dish were imaged at baseline and after 1, 4, and 18 h co-incubation using an Eclipse A1R microscope and NIS-Elements software (Nikon Instruments Inc., Melville, NY, USA). Images were analyzed as previously described [9 (link)] using High-Content Screening Navigator (HCS) Colocalization.V4 protocol (Perkin Elmer, Waltham, MA, USA); non-internalized donor mitochondria were excluded. Baseline characteristics were evaluated using HCS Morphology.V4 protocol.
Louwagie E.J., Larsen T.D., Wachal A.L., Gandy T.C, & Baack M.L. (2021). Mitochondrial Transfer Improves Cardiomyocyte Bioenergetics and Viability in Male Rats Exposed to Pregestational Diabetes. International Journal of Molecular Sciences, 22(5), 2382.
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2

Visualizing ZPFCE-NPs in BMDCs

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BMDCs labeled with ZPFCE-NPs were fixed in 4% PFA. Microscopy was performed using a confocal microscope (Nikon Eclipse A1R microscope, VIB 11, Center for the Biology of Disease, KU Leuven). Data were analyzed using the NIS Element software v4.10 (Nikon, Tokyo, Japan) and processed in Fiji software v1.49a (SC, USA).
Saini S., Vanherwegen A.S., Liang S., Verbeke R., Korf H., Lentacker I., De Smedt S.C., Gysemans C, & Himmelreich U. (2022). Fluorine MR Imaging Probes Dynamic Migratory Profiles of Perfluorocarbon-Loaded Dendritic Cells After Streptozotocin-Induced Inflammation. Molecular imaging and biology, 24(2).
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