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3i - Intelligent Imaging two-photon laser scanning microscope (2p- vivo
(A1) Time-series standard deviation projection in the sagittal plane from 2 <t>photon</t> <t>laser</t> <t>scanning</t> <t>microscope</t> showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired <t>two-tailed</t> t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).
Two Photon Laser Scanning Microscope (2p Vivo, supplied by 3i - Intelligent Imaging, 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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two-photon laser scanning microscope (2p- vivo - by Bioz Stars, 2026-07
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1) Product Images from "The Reissner fiber under tension in vivo shows dynamic interaction with ciliated cells contacting the cerebrospinal fluid"

Article Title: The Reissner fiber under tension in vivo shows dynamic interaction with ciliated cells contacting the cerebrospinal fluid

Journal: bioRxiv

doi: 10.1101/2023.02.22.529498

(A1) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired two-tailed t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).
Figure Legend Snippet: (A1) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired two-tailed t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).

Techniques Used: Standard Deviation, Laser-Scanning Microscopy, Selection, Activity Assay, Two Tailed Test



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3i - Intelligent Imaging two-photon laser scanning microscope (2p- vivo
(A1) Time-series standard deviation projection in the sagittal plane from 2 <t>photon</t> <t>laser</t> <t>scanning</t> <t>microscope</t> showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired <t>two-tailed</t> t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).
Two Photon Laser Scanning Microscope (2p Vivo, supplied by 3i - Intelligent Imaging, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/two+photon+microscope+%282p-+vivo/bio_rxiv__2023__02__22__529498-209-11-18?v=3i+-+Intelligent+Imaging
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two-photon laser scanning microscope (2p- vivo - by Bioz Stars, 2026-07
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3i - Intelligent Imaging two-photon microscope (2p-vivo
(A1) Time-series standard deviation projection in the sagittal plane from 2 <t>photon</t> <t>laser</t> <t>scanning</t> <t>microscope</t> showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired <t>two-tailed</t> t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).
Two Photon Microscope (2p Vivo, supplied by 3i - Intelligent Imaging, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/two+photon+microscope+%282p-+vivo/pmc06134141-156-6-9?v=3i+-+Intelligent+Imaging
Average 90 stars, based on 1 article reviews
two-photon microscope (2p-vivo - by Bioz Stars, 2026-07
90/100 stars
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3i - Intelligent Imaging two photon microscope (2p- vivo
(A1) Time-series standard deviation projection in the sagittal plane from 2 <t>photon</t> <t>laser</t> <t>scanning</t> <t>microscope</t> showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired <t>two-tailed</t> t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).
Two Photon Microscope (2p Vivo, supplied by 3i - Intelligent Imaging, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/two+photon+microscope+%282p-+vivo/pmc04786674-110-7-12?v=3i+-+Intelligent+Imaging
Average 90 stars, based on 1 article reviews
two photon microscope (2p- vivo - by Bioz Stars, 2026-07
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(A1) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired two-tailed t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).

Journal: bioRxiv

Article Title: The Reissner fiber under tension in vivo shows dynamic interaction with ciliated cells contacting the cerebrospinal fluid

doi: 10.1101/2023.02.22.529498

Figure Lengend Snippet: (A1) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from the Reissner fiber and CSF-cNs in the central canal of 3 dpf Tg ( sspo:sspo-GFP;pkd2l1:tagRFP;pkd2l1:GCaMP5G ) zebrafish larva before RF photoablation. (A2) Time-series standard deviation projection in the sagittal plane from 2 photon laser scanning microscope showing the signal from CSF-cNs after RF ablation performed by spiral scanning photoablation with an infrared pulsed laser tuned at 800 nm over 0.5 μm on the RF (see Methods). (B) ROI selection for ventral CSF-cNs to analyze activity before and after RF photoablation within the same cells (top). Example calcium activity traces normalized to baseline for each of the ROIs before (red) and after (black) RF photoablation over 75 s imaged at 3.45 Hz (see Methods). (C) Percentage of active ventral CSF-cNs (active is defined as having at least 1 calcium transient for the recording) before and after RF photoablation (109 cells total from 8 fish from 2 independent clutches; mean percent active before ablation = 27.72% ± 6.34% versus mean percent active after ablation = 10.59% ± 3.1%; paired two-tailed t-test: p < 0.05). (D) The ratio of active ventral CSF-cNs after RF photoablation to those active before RF photoablation, illustrating on average, a fraction (on average ± SEM: 45% ± 14%) of active ventral CSF-cNs before photoablation remain active after RF photoablation. The purple lines on the graph represent the mean and the error bars indicate the SEM. (E) Pie charts illustrating the number of events per ventral CSF-cN before and after RF photoablation (mean number of events in active cells before RF photoablation = 0.94 events / min versus mean number of events in active cells after RF photoablation = 0.87 events / min; paired two-tailed t-test: p < 0.005). *p < 0.05, ** p < 0.005 Scale bar is 20 μm (A1, A2), 10 μm (B).

Article Snippet: Two-photon spiral scanning ablations at 800 nm were performed with a two-photon laser scanning microscope (2p- vivo , Intelligent Imaging Innovations, Inc., Denver, Colorado, USA) equipped with a 20X objective (N.A.

Techniques: Standard Deviation, Laser-Scanning Microscopy, Selection, Activity Assay, Two Tailed Test