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Orca flash 4.0 v2 cmos camera

Manufactured by Zeiss

The Orca Flash 4.0 V2 CMOS camera is a high-performance device designed for scientific and industrial applications. It features a large sensor size, fast frame rates, and high resolution. The camera is capable of capturing detailed images and delivering reliable data for a variety of research and analysis purposes.

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2 protocols using orca flash 4.0 v2 cmos camera

1

Imaging of Walking Ciliated Cells

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Cells were concentrated by centrifugation (500×g for 5 min) and resuspended either in 0.5 mL of spring water in coverglass bottomed FluoroDishes (World Precision Instruments FD35-100) or in 0.2 mL spring water on a coverslip (FisherScientific, 12-545-D) for imaging. No more than three cells were kept in 0.5 mL imaging samples and only one cell was ever kept in 0.2 mL imaging samples in order to minimize cell-cell interactions. Cells were observed to exhibit spontaneous walking activity on coverglass. Walking cells in FluoroDishes were imaged under brightfield illumination using a Zeiss Z.1 Observer and Hamamatsu Orca Flash 4.0 V2 CMOS camera (C11440-22CU) with a 20x, 0.8 NA Plan-Apochromat (Zeiss) objective. Cells on coverslips were imaged under brightfield illumination with coverslips inverted over a well containing a small amount of distilled water to reduce evaporation using a Zeiss Axio Zoom.V16 and a PCO pco.dimax S1 camera. Importantly, in both imaging systems, the focal plane was set at the interface between cirri of walking cells and the glass surface upon which they were walking. Images were acquired at 0.033 seconds per frame with a 0.005 second exposure in order to capture all cirral dynamics during walking with minimal blur.
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2

Quantifying IMCL Dynamics with Resveratrol

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To monitor and quantify the effects of resveratrol incubation on IMCL accumulation in vitro over time, we first performed live cell imaging in myotubes from an untrained donor for 48 h with 1‐h intervals. Live cell imaging was performed using a FEI Corrsight spinning disk confocal microscope, equipped with an ORCA‐Flash 4.0 V2 CMOS camera, using a 40× 0.9 N.A. air objective (Zeiss) at 37°C. Bodipy 493/503 (D3922; Molecular probes, Fisher Scientific; 1:250) was added to the medium (and remained present throughout the imaging period) to visualize the LDs and CellMask (C10046; Invitrogen, Fisher Scientific; 1:1000) was used to visualize the plasma membranes. Upon thresholding the Bodipy‐derived signal, total lipid area, total LD number and average LD size were quantified in multiple wells.
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