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Ccd camera imag k6

Manufactured by Zeiss

The CCD Camera IMAG-K6 is a high-performance imaging device designed for laboratory and scientific applications. It features a charge-coupled device (CCD) sensor that captures high-quality digital images. The camera offers a resolution of 2,048 x 2,048 pixels and a pixel size of 7.4 μm. It is capable of capturing images with a 12-bit depth, providing detailed and accurate data for analysis. The IMAG-K6 is a versatile tool that can be used in a variety of laboratory settings to support scientific research and investigation.

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2 protocols using ccd camera imag k6

1

Subcellular Imaging of Photosynthetic Algae

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The effective quantum yield of PSII (Y(II); false coloured image) and near-infrared remission (NIR, 780 nm) were visualized at the subcellular level with the microscopic version of an Imaging-PAM (M-series, Heinz Walz GmbH, Herburger and Holzinger 2015 (link)). Therefore, algal filaments of Zygogonium AUT-p and Zygogonium AUT-g exhibiting different cell morphologies (younger or older filaments, different stages of aplanospore formation and pigmentation) were collected by using a stereomicroscope (Lumar V12; Carl Zeiss AG) and transferred to welled slides. A modified Axio Scope A.1 epifluorescence microscope equipped with a Zeiss Fluar 40 × 1.3 NA objective and CCD Camera IMAG-K6 controlled with ImagingWinGigE (V2.45i) software was used for image generation. Measuring light for Y(II) determination was provided by a LED (620 nm). The signal/noise ratio was not modified by a SP-Routine.
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2

Subcellular Imaging of Photosynthesis in Zygogonium

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The effective quantum yield of PSII (Y(II); false colored image) and near infrared remission (NIR, 780 nm) were visualised at the subcellular level with the microscopic version of an Imaging-PAM (M-series, Heinz Walz GmbH, Effeltrich, Germany; Herburger and Holzinger 2015 (link)). Therefore, algal filaments of Zygogonium AUT-p and Zygogonium AUT-g exhibiting different cell morphologies (younger or older filaments, different stages of aplanospore formation and pigmentation) were collected by using a stereomicroscope (Lumar V12; Carl Zeiss AG) and transferred to welled slides. A modified Axio Scope A.1 epifluorescence microscope equipped with a Zeiss Fluar 40×1.3 NA objective and CCD Camera IMAG-K6 controlled with ImagingWinGigE (V2.45i) software was used for image generation. Measuring light for Y(II) determination was provided by a LED (620 nm). The signal/noise ratio was not modified by a SP-Routine.
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