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Olympus bx 51 upright microscope
Bx 51 Upright Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 89/100, based on 51 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/bx 51 upright microscope/product/Olympus
Average 89 stars, based on 51 article reviews
Price from $9.99 to $1999.99
bx 51 upright microscope - by Bioz Stars, 2020-08
89/100 stars

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Related Articles

Microscopy:

Article Title: Spatially selective photonic crystal enhanced fluorescence and application to background reduction for biomolecule detection assays
Article Snippet: .. The imaging collection part of the setup was built upon an Olympus BX-51 upright microscope with a 4 × objective (N.A.=0.1, Olympus PLAN N) and electron multiplying CCD camera (9100-13, Hamamatsu). .. For fluorescence imaging, a bandpass emission filter (Semrock) is used.

Article Title: An Inhibitory Effect of Extracellular Ca2+ on Ca2+-Dependent Exocytosis
Article Snippet: .. For measurements of [Ca2+ ]i in cells in slices, we used the Uniblitz shutter-based fluorescence system (Vincent, Rochester, NY), a DVC1412 CCD camera (DVC, Austin, TX), and a BX-51 upright microscope (Olympus). .. The images were acquired with TILLvisION software (TILL Photonics, Planegg, Germany).

Article Title: Quantitative analyses of myelofibrosis by determining hydroxyproline
Article Snippet: .. Slides were viewed with an Olympus BX-51 upright microscope equipped with U Plan Fluorite objectives. .. Images were acquired using a DP71 digital camera and processed with the Adobe Photoshop software.

Article Title: Functional Topography and Development of Inhibitory Reticulothalamic Barreloid Projections
Article Snippet: .. Images of VGAT-Venus expression in barreloids in the left hemisphere were captured using a Leica TCS SP2 confocal microscope (Leica Microsystems, Wetzlar, Germany) or a Retiga-EX camera mounted on an Olympus BX-51 upright microscope (Olympus, Shinjuku, Tokyo, Japan). ..

Article Title: Super-resolution of fluorescence-free plasmonic nanoparticles using enhanced dark-field illumination based on wavelength-modulation
Article Snippet: .. Lab-built microscopy system of wavelength-modulation enhanced dark-field illumination A lab-built EDF illumination microscopy system ( ) was built on an Olympus BX-51 upright microscope (BX-51, Olympus, Tokyo, Japan) equipped with a CytoViva EDF illumination device (CytoViva Inc., Auburn, AL, USA) and a 100× objective lens (UPLANFLN, adjustable N.A., from 0.6 to 1.3, Olympus, Tokyo, Japan). .. An electron multiple charge-coupled device (EMCCD) camera (QuantEM, 512 SC, Photometrics, AZ, USA) and a color Nikon D3S digital camera (Tokyo, Japan) were installed on top of the microscope to simultaneously detect single-particle images.

Article Title: HIV Tat causes synapse loss in a mouse model of HIV-associated neurocognitive disorder that is independent of the classical complement cascade component C1q.
Article Snippet: .. IHC sections were imaged with a Hamamatsu ORCA-ER camera on an Olympus BX-51 upright microscope with Quioptic Optigrid optical sectioning hardware. .. The acquisition was controlled with Volocity 3DM software (PerkinElmer Life and Analytical Sciences).

Article Title: TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
Article Snippet: .. Slides were visualized using either an Olympus BX-51 upright microscope, or using a Nanozoomer automated microscope (Hamamatsu). .. Double-labeling immunofluorescence was performed on fixed paraffin-embedded sections of brain and spinal cord using the same primary antibodies against ubiquitin MAb1510 (1:500), rabbit polyclonal N-terminal TDP-43 (1:500), and rabbit polyclonal C-terminal TDP-43 (1:500), using Alexa Fluor 488- and Cy3 or 594-conjugated secondary antibodies (Molecular Probes) followed by cover slipping with Vectashield-DAPI mounting medium (Vector Laboratories).

Immunohistochemistry:

Article Title: HIV Tat causes synapse loss in a mouse model of HIV-associated neurocognitive disorder that is independent of the classical complement cascade component C1q.
Article Snippet: .. IHC sections were imaged with a Hamamatsu ORCA-ER camera on an Olympus BX-51 upright microscope with Quioptic Optigrid optical sectioning hardware. .. The acquisition was controlled with Volocity 3DM software (PerkinElmer Life and Analytical Sciences).

Fluorescence:

Article Title: An Inhibitory Effect of Extracellular Ca2+ on Ca2+-Dependent Exocytosis
Article Snippet: .. For measurements of [Ca2+ ]i in cells in slices, we used the Uniblitz shutter-based fluorescence system (Vincent, Rochester, NY), a DVC1412 CCD camera (DVC, Austin, TX), and a BX-51 upright microscope (Olympus). .. The images were acquired with TILLvisION software (TILL Photonics, Planegg, Germany).

Expressing:

Article Title: Functional Topography and Development of Inhibitory Reticulothalamic Barreloid Projections
Article Snippet: .. Images of VGAT-Venus expression in barreloids in the left hemisphere were captured using a Leica TCS SP2 confocal microscope (Leica Microsystems, Wetzlar, Germany) or a Retiga-EX camera mounted on an Olympus BX-51 upright microscope (Olympus, Shinjuku, Tokyo, Japan). ..

Imaging:

Article Title: Spatially selective photonic crystal enhanced fluorescence and application to background reduction for biomolecule detection assays
Article Snippet: .. The imaging collection part of the setup was built upon an Olympus BX-51 upright microscope with a 4 × objective (N.A.=0.1, Olympus PLAN N) and electron multiplying CCD camera (9100-13, Hamamatsu). .. For fluorescence imaging, a bandpass emission filter (Semrock) is used.

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  • 88
    Olympus bx 51 upright light microscope
    Transmitted light and confocal epifluorescence microscopy revealed MNP aggregates on cell monolayers and pores of the polyester membrane after 90 min transport studies with MNPs at high MNP concentration (0.659 mg Fe/ml). MNPs showed different aggregation patterns, depending on the magnetic field conditions (NMF, CMF, or PMF). (a) Images of supported cell monolayers captured by Olympus <t>BX-51</t> upright light microscope under bright field illumination at 1000 × magnifications (scale bar = 10 μm). (b) Images of TRITC-labeled MNPs acquired with a confocal fluorescence microscope, showing the pores of the membrane stained with LysoTracker® Green dyes after 30 min incubation under NMF, CMF, or PMF conditions (scale bar = 10 μm). The top image corresponds to a confocal plane across the PET membrane of the Transwell ™ insert, parallel to the plane of the cell monolayer. The bottom image corresponds to an orthogonal yz plane cutting across the cells and the membrane, perpendicularly to the plane of the cell monolayer. Solid bidirectional arrows indicate cytoplasm of the cells (C), pore (P), and basolateral (B) side at each yz plane.
    Bx 51 Upright Light Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 88/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bx 51 upright light microscope/product/Olympus
    Average 88 stars, based on 7 article reviews
    Price from $9.99 to $1999.99
    bx 51 upright light microscope - by Bioz Stars, 2020-08
    88/100 stars
      Buy from Supplier

    88
    Olympus upright brightfield microscope
    Transmitted light and confocal epifluorescence microscopy revealed MNP aggregates on cell monolayers and pores of the polyester membrane after 90 min transport studies with MNPs at high MNP concentration (0.659 mg Fe/ml). MNPs showed different aggregation patterns, depending on the magnetic field conditions (NMF, CMF, or PMF). (a) Images of supported cell monolayers captured by Olympus <t>BX-51</t> upright light microscope under bright field illumination at 1000 × magnifications (scale bar = 10 μm). (b) Images of TRITC-labeled MNPs acquired with a confocal fluorescence microscope, showing the pores of the membrane stained with LysoTracker® Green dyes after 30 min incubation under NMF, CMF, or PMF conditions (scale bar = 10 μm). The top image corresponds to a confocal plane across the PET membrane of the Transwell ™ insert, parallel to the plane of the cell monolayer. The bottom image corresponds to an orthogonal yz plane cutting across the cells and the membrane, perpendicularly to the plane of the cell monolayer. Solid bidirectional arrows indicate cytoplasm of the cells (C), pore (P), and basolateral (B) side at each yz plane.
    Upright Brightfield Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 88/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/upright brightfield microscope/product/Olympus
    Average 88 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    upright brightfield microscope - by Bioz Stars, 2020-08
    88/100 stars
      Buy from Supplier

    85
    Olympus bx 51 upright epifluorescence microscope
    Transmitted light and confocal epifluorescence microscopy revealed MNP aggregates on cell monolayers and pores of the polyester membrane after 90 min transport studies with MNPs at high MNP concentration (0.659 mg Fe/ml). MNPs showed different aggregation patterns, depending on the magnetic field conditions (NMF, CMF, or PMF). (a) Images of supported cell monolayers captured by Olympus <t>BX-51</t> upright light microscope under bright field illumination at 1000 × magnifications (scale bar = 10 μm). (b) Images of TRITC-labeled MNPs acquired with a confocal fluorescence microscope, showing the pores of the membrane stained with LysoTracker® Green dyes after 30 min incubation under NMF, CMF, or PMF conditions (scale bar = 10 μm). The top image corresponds to a confocal plane across the PET membrane of the Transwell ™ insert, parallel to the plane of the cell monolayer. The bottom image corresponds to an orthogonal yz plane cutting across the cells and the membrane, perpendicularly to the plane of the cell monolayer. Solid bidirectional arrows indicate cytoplasm of the cells (C), pore (P), and basolateral (B) side at each yz plane.
    Bx 51 Upright Epifluorescence Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bx 51 upright epifluorescence microscope/product/Olympus
    Average 85 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    bx 51 upright epifluorescence microscope - by Bioz Stars, 2020-08
    85/100 stars
      Buy from Supplier

    Image Search Results


    Transmitted light and confocal epifluorescence microscopy revealed MNP aggregates on cell monolayers and pores of the polyester membrane after 90 min transport studies with MNPs at high MNP concentration (0.659 mg Fe/ml). MNPs showed different aggregation patterns, depending on the magnetic field conditions (NMF, CMF, or PMF). (a) Images of supported cell monolayers captured by Olympus BX-51 upright light microscope under bright field illumination at 1000 × magnifications (scale bar = 10 μm). (b) Images of TRITC-labeled MNPs acquired with a confocal fluorescence microscope, showing the pores of the membrane stained with LysoTracker® Green dyes after 30 min incubation under NMF, CMF, or PMF conditions (scale bar = 10 μm). The top image corresponds to a confocal plane across the PET membrane of the Transwell ™ insert, parallel to the plane of the cell monolayer. The bottom image corresponds to an orthogonal yz plane cutting across the cells and the membrane, perpendicularly to the plane of the cell monolayer. Solid bidirectional arrows indicate cytoplasm of the cells (C), pore (P), and basolateral (B) side at each yz plane.

    Journal: ACS nano

    Article Title: Pulsed Magnetic Field Improves the Transport of Iron Oxide Nanoparticles through Cell Barriers

    doi: 10.1021/nn3057565

    Figure Lengend Snippet: Transmitted light and confocal epifluorescence microscopy revealed MNP aggregates on cell monolayers and pores of the polyester membrane after 90 min transport studies with MNPs at high MNP concentration (0.659 mg Fe/ml). MNPs showed different aggregation patterns, depending on the magnetic field conditions (NMF, CMF, or PMF). (a) Images of supported cell monolayers captured by Olympus BX-51 upright light microscope under bright field illumination at 1000 × magnifications (scale bar = 10 μm). (b) Images of TRITC-labeled MNPs acquired with a confocal fluorescence microscope, showing the pores of the membrane stained with LysoTracker® Green dyes after 30 min incubation under NMF, CMF, or PMF conditions (scale bar = 10 μm). The top image corresponds to a confocal plane across the PET membrane of the Transwell ™ insert, parallel to the plane of the cell monolayer. The bottom image corresponds to an orthogonal yz plane cutting across the cells and the membrane, perpendicularly to the plane of the cell monolayer. Solid bidirectional arrows indicate cytoplasm of the cells (C), pore (P), and basolateral (B) side at each yz plane.

    Article Snippet: Then, cell monolayers were washed with cold DPBS buffer, and the cells were examined using an Olympus BX-51 upright light microscope under bright field illumination.

    Techniques: Epifluorescence Microscopy, Concentration Assay, Peptide Mass Fingerprinting, Light Microscopy, Labeling, Fluorescence, Microscopy, Staining, Incubation, Positron Emission Tomography