2d-visifrap galvo frap module (VISITRON Inc)
90
Structured Review
VISITRON Inc
2d-visifrap galvo frap module
2d Visifrap Galvo Frap Module, supplied by VISITRON Inc, 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/frap+module/2d+visifrap+galvo+frap+module/pmc09020716-264-50-71
Average 90 stars, based on 1 article reviews
2d Visifrap Galvo Frap Module, supplied by VISITRON Inc, 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/frap+module/2d+visifrap+galvo+frap+module/pmc09020716-264-50-71
Average 90 stars, based on 1 article reviews
2d-visifrap galvo frap module - by Bioz Stars,
2026-10
90/100 stars
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Inverted Microscopy:Article Title: An acentriolar centrosome at the C. elegans ciliary base. Article Snippet: Live imaging in early embryos was performed primarily on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: A modified TurboID approach identifies tissue-specific centriolar components in C . elegans Article Snippet: For the experiments presented in and Figs, embryos were dissected in M9, mounted on agarose pads and filmed on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: The CTPase activity of ParB acts as a timing mechanism to control the dynamics and function of prokaryotic DNA partition complexes Article Snippet: FRAP analysis was performed with the Zeiss Axio.Observer Z1 setup described above, using a 488 nm-solid state laser and a Article Title: An outer membrane porin-lipoprotein complex modulates elongasome movement to establish cell curvature in Rhodospirillum rubrum Article Snippet: FRAP analysis was performed with an Axio Observer.Z1 inverted microscope (Carl Zeiss, Germany), equipped with a Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: Fluorescence recovery after photo-bleaching FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: Differential Requirements for Centrioles in Mitotic Centrosome Growth and Maintenance. Article Snippet: Live imaging of PCM recruitment was performed on a YokogawaCSUX1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat lens, 120 mW 405 nm and 100 mW 488 nm and 561 nm Software:Article Title: An acentriolar centrosome at the C. elegans ciliary base. Article Snippet: Live imaging in early embryos was performed primarily on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: A modified TurboID approach identifies tissue-specific centriolar components in C . elegans Article Snippet: For the experiments presented in and Figs, embryos were dissected in M9, mounted on agarose pads and filmed on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: The CTPase activity of ParB acts as a timing mechanism to control the dynamics and function of prokaryotic DNA partition complexes Article Snippet: FRAP analysis was performed with the Zeiss Axio.Observer Z1 setup described above, using a 488 nm-solid state laser and a Article Title: An outer membrane porin-lipoprotein complex modulates elongasome movement to establish cell curvature in Rhodospirillum rubrum Article Snippet: FRAP analysis was performed with an Axio Observer.Z1 inverted microscope (Carl Zeiss, Germany), equipped with a Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: Fluorescence recovery after photo-bleaching FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: Differential Requirements for Centrioles in Mitotic Centrosome Growth and Maintenance. Article Snippet: Live imaging of PCM recruitment was performed on a YokogawaCSUX1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat lens, 120 mW 405 nm and 100 mW 488 nm and 561 nm Imaging:Article Title: An acentriolar centrosome at the C. elegans ciliary base. Article Snippet: Live imaging in early embryos was performed primarily on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: A modified TurboID approach identifies tissue-specific centriolar components in C . elegans Article Snippet: For the experiments presented in and Figs, embryos were dissected in M9, mounted on agarose pads and filmed on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: The CTPase activity of ParB acts as a timing mechanism to control the dynamics and function of prokaryotic DNA partition complexes Article Snippet: FRAP analysis was performed with the Zeiss Axio.Observer Z1 setup described above, using a 488 nm-solid state laser and a Article Title: An outer membrane porin-lipoprotein complex modulates elongasome movement to establish cell curvature in Rhodospirillum rubrum Article Snippet: FRAP analysis was performed with an Axio Observer.Z1 inverted microscope (Carl Zeiss, Germany), equipped with a Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: Fluorescence recovery after photo-bleaching FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: Differential Requirements for Centrioles in Mitotic Centrosome Growth and Maintenance. Article Snippet: Live imaging of PCM recruitment was performed on a YokogawaCSUX1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat lens, 120 mW 405 nm and 100 mW 488 nm and 561 nm Fluorescence:Article Title: An acentriolar centrosome at the C. elegans ciliary base. Article Snippet: Live imaging in early embryos was performed primarily on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: A modified TurboID approach identifies tissue-specific centriolar components in C . elegans Article Snippet: For the experiments presented in and Figs, embryos were dissected in M9, mounted on agarose pads and filmed on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: The CTPase activity of ParB acts as a timing mechanism to control the dynamics and function of prokaryotic DNA partition complexes Article Snippet: FRAP analysis was performed with the Zeiss Axio.Observer Z1 setup described above, using a 488 nm-solid state laser and a Article Title: An outer membrane porin-lipoprotein complex modulates elongasome movement to establish cell curvature in Rhodospirillum rubrum Article Snippet: FRAP analysis was performed with an Axio Observer.Z1 inverted microscope (Carl Zeiss, Germany), equipped with a Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: Fluorescence recovery after photo-bleaching FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: Differential Requirements for Centrioles in Mitotic Centrosome Growth and Maintenance. Article Snippet: Live imaging of PCM recruitment was performed on a YokogawaCSUX1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat lens, 120 mW 405 nm and 100 mW 488 nm and 561 nm Confocal Microscopy:Article Title: An acentriolar centrosome at the C. elegans ciliary base. Article Snippet: Live imaging in early embryos was performed primarily on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: A modified TurboID approach identifies tissue-specific centriolar components in C . elegans Article Snippet: For the experiments presented in and Figs, embryos were dissected in M9, mounted on agarose pads and filmed on a Yokogawa CSU X1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat objective, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module, Photometrics CoolSNAP-HQ2 cooled CCD and Hamamatsu ImagEM X2 EM-CCD cameras and controlled by Article Title: The CTPase activity of ParB acts as a timing mechanism to control the dynamics and function of prokaryotic DNA partition complexes Article Snippet: FRAP analysis was performed with the Zeiss Axio.Observer Z1 setup described above, using a 488 nm-solid state laser and a Article Title: An outer membrane porin-lipoprotein complex modulates elongasome movement to establish cell curvature in Rhodospirillum rubrum Article Snippet: FRAP analysis was performed with an Axio Observer.Z1 inverted microscope (Carl Zeiss, Germany), equipped with a Article Title: A surveillance system ensures crossover formation in C. elegans Article Snippet: Fluorescence recovery after photo-bleaching FRAP was performed using Spinning disk confocal microscopy mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with 63x 1.4NA Plan Apochromat lens, 120mW 405nm and 100mW 488nm and 561nm solid-state lasers, 2D-VisiFRAP Galvo FRAP module and CoolSNAP-HQ2 cooled CCD camera controlled by Article Title: Differential Requirements for Centrioles in Mitotic Centrosome Growth and Maintenance. Article Snippet: Live imaging of PCM recruitment was performed on a YokogawaCSUX1 spinning disk confocal mounted on a Zeiss Axio Observer Z1 inverted microscope equipped with a 63x 1.4NA Plan Apochromat lens, 120 mW 405 nm and 100 mW 488 nm and 561 nm |