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it4ip Inc 3d microfluidic chip with vertically stacked chambers sandwiching a porous membrane
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Okolab USA Inc microfluidic chip stagetop incubation chamber p-736-zr1s/zr2s
a – c SoTILT3D combines a <t>microfluidic</t> chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.
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Xona Microfluidics two-chamber microfluidic chip sd150
a – c SoTILT3D combines a <t>microfluidic</t> chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.
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ibidi GmbH perfusion chamber of an ibidi microfluidic chip μ-slide vi 0.5 glass bottom
a – c SoTILT3D combines a <t>microfluidic</t> chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.
Perfusion Chamber Of An Ibidi Microfluidic Chip μ Slide Vi 0.5 Glass Bottom, supplied by ibidi GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ibidi GmbH perfusion chamber of an ibidi microfluidic chip
a – c SoTILT3D combines a <t>microfluidic</t> chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.
Perfusion Chamber Of An Ibidi Microfluidic Chip, supplied by ibidi GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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A Chip Microfluidic Chambers, supplied by Dow Corning, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Zellkraftwerk gmbh zellsafetm cells chipcytometry microfluidic chambers (chips)
a – c SoTILT3D combines a <t>microfluidic</t> chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.
Zellsafetm Cells Chipcytometry Microfluidic Chambers (Chips), supplied by Zellkraftwerk gmbh, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Momentive Performance Materials microfluidic chamber array chips for single cell capture
a – c SoTILT3D combines a <t>microfluidic</t> chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.
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a – c SoTILT3D combines a <t>microfluidic</t> chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.
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a – c SoTILT3D combines a microfluidic chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.

Journal: Nature Communications

Article Title: Whole-cell multi-target single-molecule super-resolution imaging in 3D with microfluidics and a single-objective tilted light sheet

doi: 10.1038/s41467-024-54609-z

Figure Lengend Snippet: a – c SoTILT3D combines a microfluidic chip that has a nanoprinted insert with a metalized side wall with a single-objective tilted light sheet (LS) and is compatible with epi- and transmission illumination. The geometry and size of the insert and the microfluidic chip can be flexibly adjusted for different targets. Schematics not to scale. d Scanning electron micrograph of the microfluidic chip insert design shown in ( b ). Scale bar 50 μm. Insert geometry was confirmed with conventional optical microscopy for each microfluidic chip used in this work. e The thin end of the LS imaged in a fluorescent solution. Scale bar 10 μm. The colorbar shows normalized intensity. f Fluorescent beads imaged with the 2 μm axial range double-helix point spread function (DH-PSF) at the indicated positions. Scale bar 2 μm. The colorbar shows normalized intensity. Fluorescent beads were imaged with the 2 μm DH-PSF for all 3D single-molecule data included in this work, with consistent performance across acquisitions.

Article Snippet: The microfluidic chip was mounted in a stagetop incubation chamber (P-736-ZR1S/ZR2S, OkoLab) compatible with an xy translation stage (OPH-XYS-O, Physik Instrumente) and a fine adjustment xyz piezoelectric translation stage (OPH-PINANO-XYZ, Physik Instrumente).

Techniques: Transmission Assay, Microscopy