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Deltavision omx 3d sim imaging system v4

Manufactured by GE Healthcare

The DeltaVision OMX 3D-SIM Imaging System V4 is a high-resolution fluorescence microscopy system designed for super-resolution imaging. It utilizes Structured Illumination Microscopy (SIM) technology to achieve a lateral resolution up to 100 nanometers, enabling the visualization of fine subcellular structures.

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3 protocols using deltavision omx 3d sim imaging system v4

1

Advanced Microscopy Techniques for Imaging

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Confocal imaging was performed on a Nikon A1R microscope equipped with a 40× 1.3 NA objective. Overnight imaging was performed on this microscope using a 20x air objective. Wide-field 3D imaging of fixed cells was performed on a DeltaVision OMX 3D-SIM Imaging System V4 (GE) equipped with an Olympus 60×/1.42 NA objective. Raw images were deconvolved using Softworx (Applied Precision). Wide-field imaging of the Golgi and nucleus in live cells was performed using Essen Biosciences Incucyte technology, which enables imaging inside of an incubator with a 20× objective. Zeiss Airyscan imaging was performed in either Fast Optimum mode (Figure 5 and Supporting Information Video S3) or in Super-resolution (SR) mode (Figures 3 and 6 and Supporting Information Videos S1 and S4) on a Zeiss LSM 880 Airyscan microscope equipped with a 63×/1.4 NA objective. Raw data was processed using Airyscan processing in “auto strength” mode with Zen Black software version 2.3. Linear adjustments for contrast and brightness were made to images using ImageJ.
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2

Super-Resolution Imaging Techniques for Cellular Visualization

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TIRF-SIM imaging was performed on either a custom TIRF-SIM microscope at the Janelia Research Campus as previously described17 (link) or a DeltaVision OMX SR (GE) microscope equipped with a 60× 1.42 NA objective. All 2D- and 3D-SIM imaging was performed on a DeltaVision OMX 3D-SIM Imaging System V4 (GE) equipped with an Olympus 60×/1.42 NA objective. Raw images were reconstructed using Softworx (Applied Precision). For 2D-SIM, a Weiner constant of 0.2 was used for every frame of processing. For 3D-SIM, a Weiner constant of 0.001 was used. Processed SIM images were zero-clipped to remove negative pixel values. Of note, some SIM images contain faint horizontal “stripes” that arise when imaging near the lower end of the CMOS camera’s dynamic range. Airyscan imaging was performed in Superresolution mode on a Zeiss LSM 880 Airyscan microscope equipped with a 63× 1.4 NA objective. Raw data was processed using Airyscan processing in “auto strength” mode (mean strength +/− S.D. = 5.5+/− 1.3) with Zen Black software version 2.3. Fig. 5A was collected on a Nikon A1R microscope equipped with a 40× 1.3 NA objective. Linear adjustments for contrast and brightness were made to images using ImageJ.
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3

Super-Resolution Imaging Techniques for Cellular Visualization

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TIRF-SIM imaging was performed on either a custom TIRF-SIM microscope at the Janelia Research Campus as previously described17 (link) or a DeltaVision OMX SR (GE) microscope equipped with a 60× 1.42 NA objective. All 2D- and 3D-SIM imaging was performed on a DeltaVision OMX 3D-SIM Imaging System V4 (GE) equipped with an Olympus 60×/1.42 NA objective. Raw images were reconstructed using Softworx (Applied Precision). For 2D-SIM, a Weiner constant of 0.2 was used for every frame of processing. For 3D-SIM, a Weiner constant of 0.001 was used. Processed SIM images were zero-clipped to remove negative pixel values. Of note, some SIM images contain faint horizontal “stripes” that arise when imaging near the lower end of the CMOS camera’s dynamic range. Airyscan imaging was performed in Superresolution mode on a Zeiss LSM 880 Airyscan microscope equipped with a 63× 1.4 NA objective. Raw data was processed using Airyscan processing in “auto strength” mode (mean strength +/− S.D. = 5.5+/− 1.3) with Zen Black software version 2.3. Fig. 5A was collected on a Nikon A1R microscope equipped with a 40× 1.3 NA objective. Linear adjustments for contrast and brightness were made to images using ImageJ.
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