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Csu x1

Manufactured by Teledyne
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The CSU-X1 is a compact, high-performance laboratory equipment designed for a variety of applications. It features advanced technology and precise control capabilities to support various experimental and analytical tasks. The core function of the CSU-X1 is to provide a reliable and versatile platform for conducting laboratory-based investigations and measurements.

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Lab products found in correlation

Prime bsi, by Teledyne (2 mentions) Plan apochromat 40x 1.3na oil objective, by Zeiss (1 mentions) Prime 95b scmos camera, by Teledyne (1 mentions)

Close spelling variants of this product

CSU-X1 spinning-disk (2 citations)

3 protocols using csu x1

1

Dual-channel Imaging of Transgenic Hydra

Cited 1 time
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Dual-labeled transgenic Hydra were prepared for imaging as described16 (link). Imaging was performed using a custom dual-channel spinning disc confocal microscope (Solamere Yokogawa CSU-X1) with a sCMOS camera for each channel (Teledyne-Photometrics Prime-BSI). Samples were simultaneously illuminated with both 488 nm and 561 nm lasers (Coherent OBIS). Emission light was split with a dichroic mirror sending green light to one camera and red light to the other. Cameras were aligned with pinholes and images were registered during processing. Images were captured with a frame rate of 10 frames per second using a 6X objective (Navitar HR Plan Apo 6X/0.3) and Micro-Manager software.
Hanson A., Reme R., Telerman N., Yamamoto W., Olivo-Marin J.C., Lagache T, & Yuste R. (2024). Automatic monitoring of neural activity with single-cell resolution in behaving Hydra. Scientific Reports, 14, 5083.
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2

Live Imaging of Transgenic Hydra

Cited 1 time
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Dual-labeled transgenic Hydra were prepared for imaging as described16 (link). Imaging was performed using a custom dual-channel spinning disc confocal microscope (Solamere Yokogawa CSU-X1) with a sCMOS camera for each channel (Teledyne-Photometrics Prime-BSI). Samples were simultaneously illuminated with both 488 nm and 561 nm lasers (Coherent OBIS). Emission light was split with a dichroic mirror sending green light to one camera and red light to the other. Cameras were aligned with pinholes and images were registered during processing. Images were captured with a frame rate of 10 frames per second using a 6X objective (Navitar HR Plan Apo 6X/0.3) and Micro-Manager software.
Hanson A., Reme R., Telerman N., Yamamoto W., Olivo-Marin J.C., Lagache T, & Yuste R. (2023). Automatic monitoring of whole-body neural activity in behaving Hydra. bioRxiv.
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3

Spinning Disk Confocal Imaging

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Cells were imaged with a Plan-Apochromat 40x/1.3NA oil objective on a Zeiss CSU Spinning Disk Confocal Microscope with a CSU-X1 Yokogawa spinning disk scan head on a Prime 95B sCMOS camera (Teledyne Photometrics). The 488/561/647nm laser powers were set at 100/200/20µW with 300/300/150ms exposure times, respectively.
Schiavon C.R., Zhang T., Zhao B., Moore A.S., Wales P., Andrade L., Wu M., Sung T.C., Dayn Y., Feng J.W., Quintero O.A., Shadel G.S., Grosse R, & Manor U. (2020). Actin chromobody imaging reveals sub-organellar actin dynamics. Nature methods, 17(9), 917-921.
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