fluocells prepared slide Search Results


fluocells prepared slide #1  (Fisher Scientific)
90
Fisher Scientific fluocells prepared slide #1
Confocal laser <t>microscope</t> optics with a fiber-coupled TES. Two excitation lasers at 405 and 488 nm were combined using a fiber combiner and focused on the sample plane under the objective (×40 NA0.95). Collimated fluorescence photons were focused on the core (10 μm diameter) at the end of the optical fiber, then introduced into the TES. The sample on the focal plane was scanned to accumulate an imaging data.
Fluocells Prepared Slide #1, supplied by Fisher Scientific, 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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Average 90 stars, based on 1 article reviews
fluocells prepared slide #1 - by Bioz Stars, 2026-04
90/100 stars
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fluocells prepared slide 2 bpae cells with mouse anti α tubulin bodipy fl goat anti mouse igg texas red x phalloidin and dapi  (Thermo Fisher)
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FluoCells prepared microscope slides contain multilabeled cell preparations for observation by fluorescence microscopy FluoCells prepared slide 2 contains bovine pulmonary artery endothelial cells BPAEC Texas Red X phalloidin is labeling the F actin anti bovine
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fluocells prepared slide 3 mouse kidney section with alexa fluor 488 wga alexa fluor 568 phalloidin and dapi  (Thermo Fisher)
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The FluoCells prepared slide 3 is ideal for demonstrating the optical sectioning properties of confocal microscopes Each slide contains a 16 µm cryostat section of mouse kidney stained with Alexa Fluor 488 wheat germ agglutinin
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fluocells prepared slide 1 bpae cells with mitotracker red cmxros alexa fluor 488 phalloidin and dapi  (Thermo Fisher)
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FluoCells prepared microscope slides contain fixed multi labeled cell preparations for observation by fluorescence microscopy FluoCells Prepared Slide 1 contains bovine pulmonary artery endothelial cells BPAEC MitoTracker Red CMXRos was used to stain the mitochondria
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Confocal laser microscope optics with a fiber-coupled TES. Two excitation lasers at 405 and 488 nm were combined using a fiber combiner and focused on the sample plane under the objective (×40 NA0.95). Collimated fluorescence photons were focused on the core (10 μm diameter) at the end of the optical fiber, then introduced into the TES. The sample on the focal plane was scanned to accumulate an imaging data.

Journal: Frontiers in Bioengineering and Biotechnology

Article Title: Few-Photon Spectral Confocal Microscopy for Cell Imaging Using Superconducting Transition Edge Sensor

doi: 10.3389/fbioe.2021.789709

Figure Lengend Snippet: Confocal laser microscope optics with a fiber-coupled TES. Two excitation lasers at 405 and 488 nm were combined using a fiber combiner and focused on the sample plane under the objective (×40 NA0.95). Collimated fluorescence photons were focused on the core (10 μm diameter) at the end of the optical fiber, then introduced into the TES. The sample on the focal plane was scanned to accumulate an imaging data.

Article Snippet: A prepared microscope slide (FluoCells Prepared Slide #1, Tremo Fisher Scientific, USA) was used as a test sample for cell imaging.

Techniques: Microscopy, Fluorescence, Imaging

Color image obtained by a confocal scanning microscope using a TES. A fixed cell sample stained with MitoTracker (red fluorescence for mitochondria), Alexa 488 (green fluorescence for F-actin), and DAPI (blue fluorescence for nuclei). Scanning data of 200 × 200 pixels (0.4 μm for each pixel step) is depicted as (A) RGB color and as (B) NIR images, which were obtained simultaneously. Irradiation power of excitation lasers is indicated. Exposure time of one pixel was 40 ms, and the total duration was 66 min.

Journal: Frontiers in Bioengineering and Biotechnology

Article Title: Few-Photon Spectral Confocal Microscopy for Cell Imaging Using Superconducting Transition Edge Sensor

doi: 10.3389/fbioe.2021.789709

Figure Lengend Snippet: Color image obtained by a confocal scanning microscope using a TES. A fixed cell sample stained with MitoTracker (red fluorescence for mitochondria), Alexa 488 (green fluorescence for F-actin), and DAPI (blue fluorescence for nuclei). Scanning data of 200 × 200 pixels (0.4 μm for each pixel step) is depicted as (A) RGB color and as (B) NIR images, which were obtained simultaneously. Irradiation power of excitation lasers is indicated. Exposure time of one pixel was 40 ms, and the total duration was 66 min.

Article Snippet: A prepared microscope slide (FluoCells Prepared Slide #1, Tremo Fisher Scientific, USA) was used as a test sample for cell imaging.

Techniques: Microscopy, Staining, Fluorescence, Irradiation