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Orca er ccd camera

Manufactured by PerkinElmer

The ORCA-ER CCD camera is a high-performance charge-coupled device (CCD) camera designed for scientific and industrial applications. It features a high-resolution, low-noise CCD sensor that delivers accurate and reliable imaging data. The camera is optimized for a wide range of applications, including microscopy, spectroscopy, and scientific imaging.

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4 protocols using orca er ccd camera

1

Imaging and Analysis of Meiotic Chromosome Spreads

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Immunolabeled chromosome spreads and DAPI-stained diakinesis/metaphase I nuclei were imaged using a Zeiss AxioPlan II microscope with 63× Plan Apochromat 1.4 objective and EXFO X-Cite metal halide light source. Images were captured by a Hamamatsu ORCA-ER CCD camera and processed using Volocity (Perkin Elmer) and Photoshop (Adobe) software packages. SIM analysis was performed using a Nikon N-SIM super-resolution microscope system and NIS-Elements 2 image processing software. MSH4-RNF212 colocalization was determined using NIS-Elements and co-foci were confirmed by visual inspection. Testes sections were imaged using an Axiovert 200 microscope and AxioCamMRc camera using AxioVision 4.4 software. Apoptotic cells were imaged and counted in representative fields of view.
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2

Imaging and Analysis of Meiotic Chromosome Spreads

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Immunolabeled chromosome spreads and DAPI-stained diakinesis/metaphase I nuclei were imaged using a Zeiss AxioPlan II microscope with 63× Plan Apochromat 1.4 objective and EXFO X-Cite metal halide light source. Images were captured by a Hamamatsu ORCA-ER CCD camera and processed using Volocity (Perkin Elmer) and Photoshop (Adobe) software packages. SIM analysis was performed using a Nikon N-SIM super-resolution microscope system and NIS-Elements 2 image processing software. MSH4-RNF212 colocalization was determined using NIS-Elements and co-foci were confirmed by visual inspection. Testes sections were imaged using an Axiovert 200 microscope and AxioCamMRc camera using AxioVision 4.4 software. Apoptotic cells were imaged and counted in representative fields of view.
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3

Multimodal Microscopy for Live-Cell Imaging

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Laser-scanning confocal microscopy was performed using a Leica DMI4000B microscope, with laser scanning and detection achieved by a Leica TCS SPE confocal system controlled with Leica LAS AF software. Fluorescence and wide-field microscopy was performed using a Leica DM6000B with a Leica DFC350 FX CCD camera and a Leica AF7000 with a Hamamatsu EM CCD C9100 camera and Leica LAS AF software. Leica AF7000 was also used for imaging of axon and growth cone regeneration after axotomy. Live confocal imaging was performed with an Olympus IX70 microscope using a Hamamatsu ORCA-ER CCD camera and a PerkinElmer UltraVIEW scanner for spinning disc confocal microscopy, controlled with MetaMorph software.
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4

Visualizing Mitochondrial Dynamics in Astrocytes

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Human or mouse primary astrocytes were plated on either geltrex-coated 8-well chambers (Ibidi, 80826) or on CELLview glass-bottom Petri dishes (Greiner Bio One, 627860). Cells were incubated in 500 nM MitoBright Red (a membrane potential independent dye; Dojindo, MT11; gift from Dr András Füredi) diluted in culture media and incubated for 30 min at 37 °C. Media was changed before imaging to Neurobasal without phenol and with 1% Glutamax. Images were taken by a spinning-disc confocal microscope (Olympus IX70 microscope, Hamamatsu ORCA-ER CCD camera, PerkinElmer UltraVIEW scanner controlled by the MetaMorph software) at 1 second intervals. For tracking mitochondrial movements, the TrackMate ImageJ plugin was used.
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