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axioobserver d1 inverted fluorescence microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss axioobserver d1 inverted fluorescence microscope
    Axioobserver D1 Inverted Fluorescence Microscope, supplied by Carl Zeiss, 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/inverted+fluorescence+microscope+axioobserver+d1/axio+microscope+observer+z1+%CE%B2/pm40497733-243-13-18
    Average 90 stars, based on 1 article reviews
    axioobserver d1 inverted fluorescence microscope - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Fluorescence:

    Article Title: Efficient entry of cell-penetrating peptide nona-arginine into adherent cells involves a transient increase in intracellular calcium
    Article Snippet: .. Images were acquired with an inverted fluorescence microscope (AxioObserver D1; Zeiss) equipped with a 20 × 0.8 numerical aperture (NA) Plan-Apochromat objective (Zeiss), LUDL filter wheels on both the epifluorescence illumination port and the image acquisition side port, CoolLed pE-2 LED illuminator (380, 490, 550 and 635 nm) and an Ixon 885 EMCCD camera (Andor). ..

    Article Title: The role of prospero homeobox 1 (PROX1) expression in follicular thyroid carcinoma cells
    Article Snippet: Approximately 3x10 5 cells were transiently transfected with 1 μg of YFP-expressing plasmid pIRES2-eYFP-PROX1 (pIRES-PROX1) or empty plasmid pIRES2-eYFP (pIRES; both plasmids kindly provided by Dr. J. Becker, Department of Anatomy and Cell Biology, Universitätsmedizin Göttingen UMG, Göttingen, Germany) using LIpofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. .. Cells were harvested at 48 hours following transfection, the transfection efficiency was verified under an inverted fluorescence microscope (AxioObserver D1, Zeiss, Germany), and the cells were used in functional assays. ..

    Article Title: Efficient entry of cell-penetrating peptide nona-arginine into adherent cells involves a transient increase in intracellular calcium
    Article Snippet: .. Images were acquired with an inverted fluorescence microscope (AxioObserver D1; Zeiss) equipped with a 20×0.8 numerical aperture (NA) Plan-Apochromat objective (Zeiss), LUDL filter wheels on both the epifluorescence illumination port and the image acquisition side port, CoolLed pE-2 LED illuminator (380, 490, 550 and 635 nm) and an Ixon 885 EMCCD camera (Andor). ..

    Article Title: Myosin-gelsolin cooperativity in actin filament severing and actomyosin motor activity
    Article Snippet: .. The fluorescence images of F-actin sliding on HMM were captured using an inverted fluorescence microscope (AxioObserver D1, Zeiss, Jena, Germany) with 63× planapochromat objective (Zeiss: 1.4 N.A). .. The image sequences were recorded using a digital CCD camera (C4742-95, Orca-ER, Hamamatsu Photonics, Hamamatsu, Japan) (Hamamatsu Photonics) or an EM-CCD camera (C9100, Hamamatsu Photonics) using HCImage software.

    Article Title: Myosin and gelsolin cooperate in actin filament severing and actomyosin motor activity
    Article Snippet: .. The fluorescence images of F-actin sliding on HMM were captured using an inverted fluorescence microscope (AxioObserver D1, Zeiss) with 63× plan apochromat objective (Zeiss: 1.4 N A). .. The image sequences were recorded using a digital CCD camera (C4742-95, Orca-ER, Hamamatsu Photonics) or an EM-CCD camera (C9100, Hamamatsu Photonics) using HCImage software.

    Article Title: Annexin A1 Deficiency does not Affect Myofiber Repair but Delays Regeneration of Injured Muscles
    Article Snippet: .. Images were acquired using an inverted fluorescence microscope AxioObserver D1 (Zeiss) equipped with 20 × 0.8 NA Plan-Apochromat objective (Zeiss), LUDL filter wheels on both epifluorescence illumination port and image acquisition side port, CoolLed pE-2 LED illuminator (380, 490, 550 and 635 nm), and Ixon 885 EMCCD camera (Andor). ..

    Article Title: Acoustofluidic Tweezers Integrated with Droplet Sensing Enable Multifunctional Closed-Loop Droplet Manipulation.
    Article Snippet: .. The SFITs device was then placed under an inverted fluorescence microscope (AxioObserver D1; ZEISS, Germany) for particle observation. .. Image-Based Visual Recognition: Droplet position identification was performed using MATLAB programming, based on grayscale image processing (“rgb2gray”), morphological operations (“imopen”), and connected component analysis (“regionprops”).

    Microscopy:

    Article Title: Efficient entry of cell-penetrating peptide nona-arginine into adherent cells involves a transient increase in intracellular calcium
    Article Snippet: .. Images were acquired with an inverted fluorescence microscope (AxioObserver D1; Zeiss) equipped with a 20 × 0.8 numerical aperture (NA) Plan-Apochromat objective (Zeiss), LUDL filter wheels on both the epifluorescence illumination port and the image acquisition side port, CoolLed pE-2 LED illuminator (380, 490, 550 and 635 nm) and an Ixon 885 EMCCD camera (Andor). ..

    Article Title: The role of prospero homeobox 1 (PROX1) expression in follicular thyroid carcinoma cells
    Article Snippet: Approximately 3x10 5 cells were transiently transfected with 1 μg of YFP-expressing plasmid pIRES2-eYFP-PROX1 (pIRES-PROX1) or empty plasmid pIRES2-eYFP (pIRES; both plasmids kindly provided by Dr. J. Becker, Department of Anatomy and Cell Biology, Universitätsmedizin Göttingen UMG, Göttingen, Germany) using LIpofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. .. Cells were harvested at 48 hours following transfection, the transfection efficiency was verified under an inverted fluorescence microscope (AxioObserver D1, Zeiss, Germany), and the cells were used in functional assays. ..

    Article Title: Efficient entry of cell-penetrating peptide nona-arginine into adherent cells involves a transient increase in intracellular calcium
    Article Snippet: .. Images were acquired with an inverted fluorescence microscope (AxioObserver D1; Zeiss) equipped with a 20×0.8 numerical aperture (NA) Plan-Apochromat objective (Zeiss), LUDL filter wheels on both the epifluorescence illumination port and the image acquisition side port, CoolLed pE-2 LED illuminator (380, 490, 550 and 635 nm) and an Ixon 885 EMCCD camera (Andor). ..

    Article Title: Myosin-gelsolin cooperativity in actin filament severing and actomyosin motor activity
    Article Snippet: .. The fluorescence images of F-actin sliding on HMM were captured using an inverted fluorescence microscope (AxioObserver D1, Zeiss, Jena, Germany) with 63× planapochromat objective (Zeiss: 1.4 N.A). .. The image sequences were recorded using a digital CCD camera (C4742-95, Orca-ER, Hamamatsu Photonics, Hamamatsu, Japan) (Hamamatsu Photonics) or an EM-CCD camera (C9100, Hamamatsu Photonics) using HCImage software.

    Article Title: Myosin and gelsolin cooperate in actin filament severing and actomyosin motor activity
    Article Snippet: .. The fluorescence images of F-actin sliding on HMM were captured using an inverted fluorescence microscope (AxioObserver D1, Zeiss) with 63× plan apochromat objective (Zeiss: 1.4 N A). .. The image sequences were recorded using a digital CCD camera (C4742-95, Orca-ER, Hamamatsu Photonics) or an EM-CCD camera (C9100, Hamamatsu Photonics) using HCImage software.

    Article Title: Annexin A1 Deficiency does not Affect Myofiber Repair but Delays Regeneration of Injured Muscles
    Article Snippet: .. Images were acquired using an inverted fluorescence microscope AxioObserver D1 (Zeiss) equipped with 20 × 0.8 NA Plan-Apochromat objective (Zeiss), LUDL filter wheels on both epifluorescence illumination port and image acquisition side port, CoolLed pE-2 LED illuminator (380, 490, 550 and 635 nm), and Ixon 885 EMCCD camera (Andor). ..

    Article Title: Acoustofluidic Tweezers Integrated with Droplet Sensing Enable Multifunctional Closed-Loop Droplet Manipulation.
    Article Snippet: .. The SFITs device was then placed under an inverted fluorescence microscope (AxioObserver D1; ZEISS, Germany) for particle observation. .. Image-Based Visual Recognition: Droplet position identification was performed using MATLAB programming, based on grayscale image processing (“rgb2gray”), morphological operations (“imopen”), and connected component analysis (“regionprops”).

    Transfection:

    Article Title: The role of prospero homeobox 1 (PROX1) expression in follicular thyroid carcinoma cells
    Article Snippet: Approximately 3x10 5 cells were transiently transfected with 1 μg of YFP-expressing plasmid pIRES2-eYFP-PROX1 (pIRES-PROX1) or empty plasmid pIRES2-eYFP (pIRES; both plasmids kindly provided by Dr. J. Becker, Department of Anatomy and Cell Biology, Universitätsmedizin Göttingen UMG, Göttingen, Germany) using LIpofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. .. Cells were harvested at 48 hours following transfection, the transfection efficiency was verified under an inverted fluorescence microscope (AxioObserver D1, Zeiss, Germany), and the cells were used in functional assays. ..

    Functional Assay:

    Article Title: The role of prospero homeobox 1 (PROX1) expression in follicular thyroid carcinoma cells
    Article Snippet: Approximately 3x10 5 cells were transiently transfected with 1 μg of YFP-expressing plasmid pIRES2-eYFP-PROX1 (pIRES-PROX1) or empty plasmid pIRES2-eYFP (pIRES; both plasmids kindly provided by Dr. J. Becker, Department of Anatomy and Cell Biology, Universitätsmedizin Göttingen UMG, Göttingen, Germany) using LIpofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. .. Cells were harvested at 48 hours following transfection, the transfection efficiency was verified under an inverted fluorescence microscope (AxioObserver D1, Zeiss, Germany), and the cells were used in functional assays. ..



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