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Structured Review

Thorlabs cage rotation mount for ø1 optics
System description. The path first passes through an optical density filter wheel (1), then a half‐wave slide (2a), then a beam expander (3), a polarization splitter cube (4), a second half‐wave slide (2b), a microdisplay called a spatial light modulator (SLM) (5), a quarter‐wave slide (7), an achromatic lens (8) with focal length f = 40 cm, and ends up at the microscope's epifluorescence illumination input.
Cage Rotation Mount For ø1 Optics, supplied by Thorlabs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cage+rotation+mount+for+%C3%B81+optics/mount+rotation/pmc12968945-17-0-7
Average 86 stars, based on 1 article reviews
cage rotation mount for ø1 optics - by Bioz Stars, 2026-10
86/100 stars

Images

1) Product Images from "Implementation and Optimization of a Random Illumination Microscope: towards Robustness for Microscopy Core Facility"

Article Title: Implementation and Optimization of a Random Illumination Microscope: towards Robustness for Microscopy Core Facility

Journal: Biology of the Cell

doi: 10.1111/boc.70060

System description. The path first passes through an optical density filter wheel (1), then a half‐wave slide (2a), then a beam expander (3), a polarization splitter cube (4), a second half‐wave slide (2b), a microdisplay called a spatial light modulator (SLM) (5), a quarter‐wave slide (7), an achromatic lens (8) with focal length f = 40 cm, and ends up at the microscope's epifluorescence illumination input.
Figure Legend Snippet: System description. The path first passes through an optical density filter wheel (1), then a half‐wave slide (2a), then a beam expander (3), a polarization splitter cube (4), a second half‐wave slide (2b), a microdisplay called a spatial light modulator (SLM) (5), a quarter‐wave slide (7), an achromatic lens (8) with focal length f = 40 cm, and ends up at the microscope's epifluorescence illumination input.

Techniques Used: Microscopy

Choice of AlgoRIM reconstruction parameters. (A) Reconstructed image of 0.1 µm beads. (B) Plot profile along the line in A by modifying the pre‐filtering parameter (Wiener filtering or w) and the regularization parameter (r). (C) Reconstruction result by modifying the various w ‐ and r ‐ values.
Figure Legend Snippet: Choice of AlgoRIM reconstruction parameters. (A) Reconstructed image of 0.1 µm beads. (B) Plot profile along the line in A by modifying the pre‐filtering parameter (Wiener filtering or w) and the regularization parameter (r). (C) Reconstruction result by modifying the various w ‐ and r ‐ values.

Techniques Used:

Comparison of microvilli observation between the RIM system and confocal Airyscan (Zeiss). Microvilli brush border intestine were identified by ERM‐1/ezrin tagged with mNeonGreen and visualized in adult C. elegans .
Figure Legend Snippet: Comparison of microvilli observation between the RIM system and confocal Airyscan (Zeiss). Microvilli brush border intestine were identified by ERM‐1/ezrin tagged with mNeonGreen and visualized in adult C. elegans .

Techniques Used: Comparison

Related Articles

Microscopy:

Article Title: Implementation and Optimization of a Random Illumination Microscope: towards Robustness for Microscopy Core Facility
Article Snippet: Cage Rotation Mount for Ø1′′ Optics , Thorlabs , CRM1T/M.

Comparison:

Article Title: Implementation and Optimization of a Random Illumination Microscope: towards Robustness for Microscopy Core Facility
Article Snippet: Cage Rotation Mount for Ø1′′ Optics , Thorlabs , CRM1T/M.



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System description. The path first passes through an optical density filter wheel (1), then a half‐wave slide (2a), then a beam expander (3), a polarization splitter cube (4), a second half‐wave slide (2b), a microdisplay called a spatial light modulator (SLM) (5), a quarter‐wave slide (7), an achromatic lens (8) with focal length f = 40 cm, and ends up at the microscope's epifluorescence illumination input.
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Image Search Results


System description. The path first passes through an optical density filter wheel (1), then a half‐wave slide (2a), then a beam expander (3), a polarization splitter cube (4), a second half‐wave slide (2b), a microdisplay called a spatial light modulator (SLM) (5), a quarter‐wave slide (7), an achromatic lens (8) with focal length f = 40 cm, and ends up at the microscope's epifluorescence illumination input.

Journal: Biology of the Cell

Article Title: Implementation and Optimization of a Random Illumination Microscope: towards Robustness for Microscopy Core Facility

doi: 10.1111/boc.70060

Figure Lengend Snippet: System description. The path first passes through an optical density filter wheel (1), then a half‐wave slide (2a), then a beam expander (3), a polarization splitter cube (4), a second half‐wave slide (2b), a microdisplay called a spatial light modulator (SLM) (5), a quarter‐wave slide (7), an achromatic lens (8) with focal length f = 40 cm, and ends up at the microscope's epifluorescence illumination input.

Article Snippet: Cage Rotation Mount for Ø1′′ Optics , Thorlabs , CRM1T/M.

Techniques: Microscopy

Choice of AlgoRIM reconstruction parameters. (A) Reconstructed image of 0.1 µm beads. (B) Plot profile along the line in A by modifying the pre‐filtering parameter (Wiener filtering or w) and the regularization parameter (r). (C) Reconstruction result by modifying the various w ‐ and r ‐ values.

Journal: Biology of the Cell

Article Title: Implementation and Optimization of a Random Illumination Microscope: towards Robustness for Microscopy Core Facility

doi: 10.1111/boc.70060

Figure Lengend Snippet: Choice of AlgoRIM reconstruction parameters. (A) Reconstructed image of 0.1 µm beads. (B) Plot profile along the line in A by modifying the pre‐filtering parameter (Wiener filtering or w) and the regularization parameter (r). (C) Reconstruction result by modifying the various w ‐ and r ‐ values.

Article Snippet: Cage Rotation Mount for Ø1′′ Optics , Thorlabs , CRM1T/M.

Techniques:

Comparison of microvilli observation between the RIM system and confocal Airyscan (Zeiss). Microvilli brush border intestine were identified by ERM‐1/ezrin tagged with mNeonGreen and visualized in adult C. elegans .

Journal: Biology of the Cell

Article Title: Implementation and Optimization of a Random Illumination Microscope: towards Robustness for Microscopy Core Facility

doi: 10.1111/boc.70060

Figure Lengend Snippet: Comparison of microvilli observation between the RIM system and confocal Airyscan (Zeiss). Microvilli brush border intestine were identified by ERM‐1/ezrin tagged with mNeonGreen and visualized in adult C. elegans .

Article Snippet: Cage Rotation Mount for Ø1′′ Optics , Thorlabs , CRM1T/M.

Techniques: Comparison

Journal: HardwareX

Article Title: Multimodal fluorescence microscope with fast adaptive polarimetry

doi: 10.1016/j.ohx.2023.e00480

Figure Lengend Snippet:

Article Snippet: Rotating mount , 30mm Cage Rotation Mount for Ø1” Optics, SM1 Threaded , 5 , 85.49 , 427.45 , Thorlabs CRM1T/M , Optomech..

Techniques: Fluorescence, Blocking Assay, Polymer