labview-based imaging software Search Results


labview software sidfthermo  (Phasics SA)
90
Phasics SA labview software sidfthermo
Labview Software Sidfthermo, supplied by Phasics SA, 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/labview-based+imaging+software/labview+software+sidfthermo/pm35965781-216-1-5
Average 90 stars, based on 1 article reviews
labview software sidfthermo - by Bioz Stars, 2026-10
90/100 stars
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labview software  (Phasics SA)
90
Phasics SA labview software
Labview Software, supplied by Phasics SA, 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/labview-based+imaging+software/labview+software/pm35965781-216-2-5
Average 90 stars, based on 1 article reviews
labview software - by Bioz Stars, 2026-10
90/100 stars
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image grabber av.io hd  (Epiphan Video)
90
Epiphan Video image grabber av.io hd
Image Grabber Av.Io Hd, supplied by Epiphan Video, 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/labview-based+imaging+software/external+video+capture+system+av+io+hd+frame+grabber/pm38241380-313-8-12
Average 90 stars, based on 1 article reviews
image grabber av.io hd - by Bioz Stars, 2026-10
90/100 stars
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av.io hd™  (Epiphan Video)
90
Epiphan Video av.io hd™
Av.Io Hd™, supplied by Epiphan Video, 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/labview-based+imaging+software/av+io+hd+/bio_rxiv__2023__02__16__528823-241-1-5
Average 90 stars, based on 1 article reviews
av.io hd™ - by Bioz Stars, 2026-10
90/100 stars
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fv1000-mpe software  (Becton Dickinson)
90
Becton Dickinson fv1000-mpe software
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
Fv1000 Mpe Software, supplied by Becton Dickinson, 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/labview-based+imaging+software/fv1000+mpe+software/pmc03269225-238-0-3
Average 90 stars, based on 1 article reviews
fv1000-mpe software - by Bioz Stars, 2026-10
90/100 stars
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25x 1 05 na  (Nikon)
99
Nikon 25x 1 05 na
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
25x 1 05 Na, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/labview-based+imaging+software/Objectives/pmc07237886-266-13-16
Average 99 stars, based on 1 article reviews
25x 1 05 na - by Bioz Stars, 2026-10
99/100 stars
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x-ray biplane angiographic unit  (TOSHIBA Medical)
90
TOSHIBA Medical x-ray biplane angiographic unit
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
X Ray Biplane Angiographic Unit, supplied by TOSHIBA Medical, 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/labview-based+imaging+software/x+ray+biplane+angiographic+unit/pmc03419595-60-18-22
Average 90 stars, based on 1 article reviews
x-ray biplane angiographic unit - by Bioz Stars, 2026-10
90/100 stars
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high-speed scientific cmos camera hamamatsu flash 4.0  (Hamamatsu)
90
Hamamatsu high-speed scientific cmos camera hamamatsu flash 4.0
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
High Speed Scientific Cmos Camera Hamamatsu Flash 4.0, supplied by Hamamatsu, 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/labview-based+imaging+software/em+ccd+camera/pmc07599336-329-8-12
Average 90 stars, based on 1 article reviews
high-speed scientific cmos camera hamamatsu flash 4.0 - by Bioz Stars, 2026-10
90/100 stars
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origin 2016  (OriginLab corp)
90
OriginLab corp origin 2016
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
Origin 2016, supplied by OriginLab corp, 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/labview-based+imaging+software/origin+2016/pm32789375-67-44-46
Average 90 stars, based on 1 article reviews
origin 2016 - by Bioz Stars, 2026-10
90/100 stars
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custom-built confocal/multiphoton microscope  (Coleman Technologies)
90
Coleman Technologies custom-built confocal/multiphoton microscope
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
Custom Built Confocal/Multiphoton Microscope, supplied by Coleman Technologies, 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/labview-based+imaging+software/custom+built+confocal+multiphoton+microscope/pmc02828910-68-10-61
Average 90 stars, based on 1 article reviews
custom-built confocal/multiphoton microscope - by Bioz Stars, 2026-10
90/100 stars
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coreldraw graphics suite 2017 v19.1.0.419  (corel corporation)
90
corel corporation coreldraw graphics suite 2017 v19.1.0.419
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
Coreldraw Graphics Suite 2017 V19.1.0.419, supplied by corel corporation, 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/labview-based+imaging+software/coreldraw+graphics+suite+2017/pm34233161-664-42-43
Average 90 stars, based on 1 article reviews
coreldraw graphics suite 2017 v19.1.0.419 - by Bioz Stars, 2026-10
90/100 stars
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ccd camera evolution qei  (QImaging)
90
QImaging ccd camera evolution qei
Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by <t>FV1000-MPE</t> software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.
Ccd Camera Evolution Qei, supplied by QImaging, 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/labview-based+imaging+software/ccd+camera+evolution+qei/pmc07846278-315-1-5
Average 90 stars, based on 1 article reviews
ccd camera evolution qei - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by FV1000-MPE software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.

Journal: Neural Systems & Circuits

Article Title: Simultaneous two-photon activation of presynaptic cells and calcium imaging in postsynaptic dendritic spines

doi: 10.1186/2042-1001-1-2

Figure Lengend Snippet: Diagram of the hardware of simultaneous Ca 2+ imaging and 2pMAPG mapping . Two mode-locked femtosecond-pulse Ti:sapphire lasers set at 830 nm and 720 nm were connected to the laser-scanning microscope via two independent scanheads. The laser beam illumination times and diameters were regulated by acoustic optical modulators (AOMs) and collimating lens, respectively. A pyramidal cell in the cortical slice was patch-clamped and loaded with Alexa Fluor 594 and Fluo-5F. Extracellular solution containing caged glutamate was oxygenated and re-circulated continuously. On the PC screen, the Ca 2+ imaging region (left) and 2pMAPG mapping area (right) were chosen. The imaging plane and mapping plane were changed rapidly by the piezo actuator attached to the objective. AOMs, Galvano mirrors, and the piezo actuator were regulated by FV1000-MPE software. Simultaneously, electric signals from the patch-clamp amplifier and from two photomultiplier tubes for detecting red and green fluorescence were recorded. If a photostimulated neuron innervated one of the spines in the imaging region, Ca 2+ transients were observed in this spine (yellow in the PC screen). See the details in the main text.

Article Snippet: FV1000-MPE software, IPLab (BD Biosciences, MD, USA) and our own software programs based on LabView (National Instruments, TX, USA) were used for image processing.

Techniques: Imaging, Laser-Scanning Microscopy, Software, Patch Clamp, Fluorescence