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Axiocam 506 mono ccd camera

Manufactured by Zeiss
Sourced in Germany

The Axiocam 506 mono is a high-performance CCD camera by Zeiss. It features a 5.0 megapixel monochrome sensor with a pixel size of 5.5 μm. The camera supports resolutions up to 2560 x 2048 pixels and offers a frame rate of up to 40 frames per second.

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3 protocols using axiocam 506 mono ccd camera

1

Microscopy Imaging of Biological Samples

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Bright and dark field pictures were taken on a Zeiss Axioplan 2 microscope with a SPOT 14.2 camera and SPOT advanced software (Diagnostic Instruments), radioactive in situ hybridization signals were visualized using the illuminator Intralux 5000–1 (Volpi). Fluorescence pictures were taken on a Zeiss Axiovert 200 microscope with a Spot 23.0 camera (Diagnostic Instruments) and Metamorph imaging software (Visitron Imaging Systems) or a Zeiss Axio Observer 7 microscope with an AxioCam 506 mono CCD camera (Zeiss) and Zen 2.3 software (Zeiss).
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2

Tracking Erythroid Progenitor Cell Cycle

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Erythroid progenitors were seeded at 4–5 × 105 cells/ml on fibronectin‐coated μl‐slide eight‐well ibiTreat (ibidi) and allowed to adhere for 1 h at 37°C, 5% CO2. Cells were imaged for 48 h at 37°C, 5% CO2 at a single focal plane in bright field using a Zeiss Axio observer Z1 inverted microscope equipped with an environmental chamber, and either an ORCA‐Flash 4.0 CMOS camera (Hamamatsu) and a Plan‐Apochromat 40×/0.95 Ph3 DIC objective (Zeiss) or an Axiocam 506 mono CCD camera (Zeiss) and a LD Plan‐Neofluar 40×/0.6 Ph2 DIC objective (Zeiss). Zen Blue software (Zeiss) was used for data collection and analysis. To quantify cell cycle timing, the duration between each cytokinesis was scored by following two daughter cells until they stopped dividing, died, or enucleated.
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3

Bright Field and Fluorescence Imaging of DAB Staining in DRG Cryosections

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For bright field image acquisition of DAB staining on DRG cryosections, we used a Leica DMI IL LED inverted microscope with a DMC2900 CCD camera (Leica Microsystems, Wetzlar, Germany). Images were acquired with the Leica Application Suite X software (Leica Microsystems, Wetzlar, Germany) at 20× magnification and were used for cell counting of CD11b+ and CD3+ cells in DRG sections. For fluorescence image acquisition, we used the fluorescence microscope Zeiss Imager M.2 with an Apotome 2 device for structured illumination, Colibri 7 LED as a light source, and an Axiocam 506 mono CCD camera (all Zeiss, Oberkochen, Germany), and the fluorescence microscope Zeiss Axiophot 2 (Zeiss, Oberkochen, Germany) equipped with a SPOT INSIGHTTM 4.0 Mp Color Camera and the SPOT Advanced Software (both SPOT imaging, Sterling Heights, MI, USA). Images were acquired with the Zeiss ZEN Blue edition software at 20× magnification.
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