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confocal fluorescence imaging system nikon d-eclipse c1  (Nikon)


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    Nikon confocal fluorescence imaging system nikon d-eclipse c1
    Confocal Fluorescence Imaging System Nikon D Eclipse C1, supplied by Nikon, 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/confocal+imaging+system+nikon+d-eclipse+c1/pm29341492-103-12-16
    Average 90 stars, based on 1 article reviews
    confocal fluorescence imaging system nikon d-eclipse c1 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Microscopy:

    Article Title: An NBD Derivative of the Selective Rat Toxicant Norbormide as a New Probe for Living Cell Imaging
    Article Snippet: Finally, coverslips were mounted on microscope slides using Mowiol 40–88 (Sigma Aldrich). .. Confocal images were acquired with a Laser Scanning Confocal Microscope (LSCM) D-Eclipse C1 SHV Nikon system equipped with a Nikon Eclipse E600 microscope and 3 laser diode modules (488/543/637 nm), using a CFI Plan Apochromat 60x NA 1.4 objective and analyzed using NIS Elements software (Nikon) and the open-source platform for biological-image analysis Fiji software. ..

    Article Title: Hedgehog signaling regulates ciliary localization of mouse odorant receptors
    Article Snippet: .. Imaging was done with Nikon D eclipse C1 confocal system equipped with Nikon eclipse 90i microscope using plan APO VC 60× 1.40 N.A. objective and with a Leica TCS SPE confocal system equipped with a Leica DM5500Q microscope using PL APO 63× 1.4 N.A. objective. .. Leica TCS SPE confocal images were acquired with 0.50-μm voxel size either with 0.10 × 0.10 or 0.07 × 0.07 μm 2 pixel size.

    Article Title: Winner of the society for biomaterials student award in the Ph.D. category for the annual meeting of the society for biomaterials, april 11-14, 2018, Atlanta, GA: Development of a bimodal, in situ crosslinking method to achieve multifactor release from electrospun gelatin.
    Article Snippet: 2 To better mimic native tissue microenvironments, current efforts have moved beyond single growth factor delivery to more complex multiple growth factor delivery with distinct release profiles.. Electrospun gelatin, a widely investigated drug delivery vehicle, requires postprocessing crosslinking techniques that generate a mesh with uniform crosslinking density, limiting the ability to deliver multiple factors at different rates.. Herein, we describe a method to independently control release of multiple factors from a single electrospun gelatin mesh.

    Article Title: κ-Opioid Receptor Is Colocalized in GnRH and KNDy Cells in the Female Ovine and Rat Brain
    Article Snippet: .. Confocal imaging Sections processed for dual immunofluorescence were imaged using a Nikon D-Eclipse C1 laser-scanning confocal system (Nikon Corp) attached to a Nikon Eclipse E800 microscope (Nikon Corp). ..

    Software:

    Article Title: An NBD Derivative of the Selective Rat Toxicant Norbormide as a New Probe for Living Cell Imaging
    Article Snippet: Finally, coverslips were mounted on microscope slides using Mowiol 40–88 (Sigma Aldrich). .. Confocal images were acquired with a Laser Scanning Confocal Microscope (LSCM) D-Eclipse C1 SHV Nikon system equipped with a Nikon Eclipse E600 microscope and 3 laser diode modules (488/543/637 nm), using a CFI Plan Apochromat 60x NA 1.4 objective and analyzed using NIS Elements software (Nikon) and the open-source platform for biological-image analysis Fiji software. ..

    Imaging:

    Article Title: Hedgehog signaling regulates ciliary localization of mouse odorant receptors
    Article Snippet: .. Imaging was done with Nikon D eclipse C1 confocal system equipped with Nikon eclipse 90i microscope using plan APO VC 60× 1.40 N.A. objective and with a Leica TCS SPE confocal system equipped with a Leica DM5500Q microscope using PL APO 63× 1.4 N.A. objective. .. Leica TCS SPE confocal images were acquired with 0.50-μm voxel size either with 0.10 × 0.10 or 0.07 × 0.07 μm 2 pixel size.

    Article Title: Kinetics of migration of colloidal particles in meat muscles in the absence and presence of a proteolytic enzyme to simulate non-motile bacteria penetration.
    Article Snippet: Contents lists available at ScienceDirect Food Research International j ourna l homepage: www.e lsev ie r .com/ locate / foodres Kinetics of migration of colloidal particles inmeat muscles in the absence and presence of a proteolytic enzyme to simulate non-motile bacteria penetration Ramona Bosse (née Danz) a, Monika Gibis a, Herbert Schmidt b, Jochen Weiss a,⁎ a Department of Food Physics and Meat Science, Institute of Food Science and Biotechnology, University of Hohenheim, 70593 Stuttgart, Germany b Department of Food Microbiology and Hygiene, Institute of Food Science and Biotechnology, University of Hohenheim, 70593 Stuttgart, Germany ⁎ Corresponding author.. E-mail address: j.weiss@uni-hohenheim.de (J. Weiss). http://dx.doi.org/10.1016/j.foodres.2015.05.054 0963-9969/© 2015 Published by Elsevier Ltd. a b s t r a c t a r t i c l e i n f o Article history: Received 20 March 2015 Received in revised form 22 May 2015 Accepted 27 May 2015 Available online 01 June 2015 Keywords: Particle distribution Bacteria simulation Spatial distribution Meat tissue Protease Microscopy In this study, migration rate and spatial distribution of colloidal particles with and without proteolytic enzymes were studied after injection in pork loinmuscle cubes for 5 days at 25 °C to simulate behavior of non-motile bacteria.. Samplesweremonitored daily by lightmicroscopy and confocal laser scanningmicroscopy and particle distribution andmovement analyzed by image analysis (MATLAB®).

    Article Title: Winner of the society for biomaterials student award in the Ph.D. category for the annual meeting of the society for biomaterials, april 11-14, 2018, Atlanta, GA: Development of a bimodal, in situ crosslinking method to achieve multifactor release from electrospun gelatin.
    Article Snippet: 2 To better mimic native tissue microenvironments, current efforts have moved beyond single growth factor delivery to more complex multiple growth factor delivery with distinct release profiles.. Electrospun gelatin, a widely investigated drug delivery vehicle, requires postprocessing crosslinking techniques that generate a mesh with uniform crosslinking density, limiting the ability to deliver multiple factors at different rates.. Herein, we describe a method to independently control release of multiple factors from a single electrospun gelatin mesh.

    Article Title: κ-Opioid Receptor Is Colocalized in GnRH and KNDy Cells in the Female Ovine and Rat Brain
    Article Snippet: .. Confocal imaging Sections processed for dual immunofluorescence were imaged using a Nikon D-Eclipse C1 laser-scanning confocal system (Nikon Corp) attached to a Nikon Eclipse E800 microscope (Nikon Corp). ..

    Inverted Microscopy:

    Article Title: Kinetics of migration of colloidal particles in meat muscles in the absence and presence of a proteolytic enzyme to simulate non-motile bacteria penetration.
    Article Snippet: Contents lists available at ScienceDirect Food Research International j ourna l homepage: www.e lsev ie r .com/ locate / foodres Kinetics of migration of colloidal particles inmeat muscles in the absence and presence of a proteolytic enzyme to simulate non-motile bacteria penetration Ramona Bosse (née Danz) a, Monika Gibis a, Herbert Schmidt b, Jochen Weiss a,⁎ a Department of Food Physics and Meat Science, Institute of Food Science and Biotechnology, University of Hohenheim, 70593 Stuttgart, Germany b Department of Food Microbiology and Hygiene, Institute of Food Science and Biotechnology, University of Hohenheim, 70593 Stuttgart, Germany ⁎ Corresponding author.. E-mail address: j.weiss@uni-hohenheim.de (J. Weiss). http://dx.doi.org/10.1016/j.foodres.2015.05.054 0963-9969/© 2015 Published by Elsevier Ltd. a b s t r a c t a r t i c l e i n f o Article history: Received 20 March 2015 Received in revised form 22 May 2015 Accepted 27 May 2015 Available online 01 June 2015 Keywords: Particle distribution Bacteria simulation Spatial distribution Meat tissue Protease Microscopy In this study, migration rate and spatial distribution of colloidal particles with and without proteolytic enzymes were studied after injection in pork loinmuscle cubes for 5 days at 25 °C to simulate behavior of non-motile bacteria.. Samplesweremonitored daily by lightmicroscopy and confocal laser scanningmicroscopy and particle distribution andmovement analyzed by image analysis (MATLAB®).

    Staining:

    Article Title: Kinetics of migration of colloidal particles in meat muscles in the absence and presence of a proteolytic enzyme to simulate non-motile bacteria penetration.
    Article Snippet: Contents lists available at ScienceDirect Food Research International j ourna l homepage: www.e lsev ie r .com/ locate / foodres Kinetics of migration of colloidal particles inmeat muscles in the absence and presence of a proteolytic enzyme to simulate non-motile bacteria penetration Ramona Bosse (née Danz) a, Monika Gibis a, Herbert Schmidt b, Jochen Weiss a,⁎ a Department of Food Physics and Meat Science, Institute of Food Science and Biotechnology, University of Hohenheim, 70593 Stuttgart, Germany b Department of Food Microbiology and Hygiene, Institute of Food Science and Biotechnology, University of Hohenheim, 70593 Stuttgart, Germany ⁎ Corresponding author.. E-mail address: j.weiss@uni-hohenheim.de (J. Weiss). http://dx.doi.org/10.1016/j.foodres.2015.05.054 0963-9969/© 2015 Published by Elsevier Ltd. a b s t r a c t a r t i c l e i n f o Article history: Received 20 March 2015 Received in revised form 22 May 2015 Accepted 27 May 2015 Available online 01 June 2015 Keywords: Particle distribution Bacteria simulation Spatial distribution Meat tissue Protease Microscopy In this study, migration rate and spatial distribution of colloidal particles with and without proteolytic enzymes were studied after injection in pork loinmuscle cubes for 5 days at 25 °C to simulate behavior of non-motile bacteria.. Samplesweremonitored daily by lightmicroscopy and confocal laser scanningmicroscopy and particle distribution andmovement analyzed by image analysis (MATLAB®).

    Fluorescence:

    Article Title: Winner of the society for biomaterials student award in the Ph.D. category for the annual meeting of the society for biomaterials, april 11-14, 2018, Atlanta, GA: Development of a bimodal, in situ crosslinking method to achieve multifactor release from electrospun gelatin.
    Article Snippet: 2 To better mimic native tissue microenvironments, current efforts have moved beyond single growth factor delivery to more complex multiple growth factor delivery with distinct release profiles.. Electrospun gelatin, a widely investigated drug delivery vehicle, requires postprocessing crosslinking techniques that generate a mesh with uniform crosslinking density, limiting the ability to deliver multiple factors at different rates.. Herein, we describe a method to independently control release of multiple factors from a single electrospun gelatin mesh.

    Immunofluorescence:

    Article Title: κ-Opioid Receptor Is Colocalized in GnRH and KNDy Cells in the Female Ovine and Rat Brain
    Article Snippet: .. Confocal imaging Sections processed for dual immunofluorescence were imaged using a Nikon D-Eclipse C1 laser-scanning confocal system (Nikon Corp) attached to a Nikon Eclipse E800 microscope (Nikon Corp). ..



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