Review



axiovert 200m fluorescence micro-scope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss axiovert 200m fluorescence micro-scope
    (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss <t>Axiovert</t> <t>200M</t> <t>Fluorescence</t> Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.
    Axiovert 200m Fluorescence Micro Scope, 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/axiovert+200m+scope/micro+scope/pmc11667565-115-9-13
    Average 90 stars, based on 1 article reviews
    axiovert 200m fluorescence micro-scope - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Therapeutic Potential of Feline Adipose-Derived Stem Cell Exosomes in the Treatment of Feline Idiopathic Cystitis: A Characterization and Functional Analysis of miRNA Content"

    Article Title: Therapeutic Potential of Feline Adipose-Derived Stem Cell Exosomes in the Treatment of Feline Idiopathic Cystitis: A Characterization and Functional Analysis of miRNA Content

    Journal: Nanotheranostics

    doi: 10.7150/ntno.99383

    (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss Axiovert 200M Fluorescence Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.
    Figure Legend Snippet: (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss Axiovert 200M Fluorescence Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.

    Techniques Used: Imaging, Derivative Assay, Staining, Fluorescence, Microscopy

    Related Articles

    Software:

    Article Title: Central role of T helper 17 cells in chronic hypoxia-induced pulmonary hypertension
    Article Snippet: Lung sections (5 μm) were stained with rabbit anti-smooth muscle α-actin (Ab5694; Abcam, Cambridge, MA) ( 39 , 52 ) antibody or rabbit IgG control (negative) followed by DyLight 549-donkey anti-rabbit (Thermo Fisher Scientific). .. Sections were examined using a ×20 or ×40 objective on a Zeiss Axiovert 200M scope and images acquired with a Cool Snap EZ camera using NIS-Elements F 3.0 software. ..

    Article Title: Nitric Oxide Modulates TGF-?-Directive Signals To Suppress Foxp3 + Regulatory T Cell Differentiation and Potentiate Th1 Development
    Article Snippet: .. Coverslips were mounted with FluorSave (Calbiochem) reagent, and immunofluorescence was analyzed under the Zeiss Axiovert 200M scope (Carl Zeiss), integrated with 3i’s Slidebook 4.2 software (Intelligent Imaging Innovations). ..

    Fluorsave:

    Article Title: Nitric Oxide Modulates TGF-?-Directive Signals To Suppress Foxp3 + Regulatory T Cell Differentiation and Potentiate Th1 Development
    Article Snippet: .. Coverslips were mounted with FluorSave (Calbiochem) reagent, and immunofluorescence was analyzed under the Zeiss Axiovert 200M scope (Carl Zeiss), integrated with 3i’s Slidebook 4.2 software (Intelligent Imaging Innovations). ..

    Immunofluorescence:

    Article Title: Nitric Oxide Modulates TGF-?-Directive Signals To Suppress Foxp3 + Regulatory T Cell Differentiation and Potentiate Th1 Development
    Article Snippet: .. Coverslips were mounted with FluorSave (Calbiochem) reagent, and immunofluorescence was analyzed under the Zeiss Axiovert 200M scope (Carl Zeiss), integrated with 3i’s Slidebook 4.2 software (Intelligent Imaging Innovations). ..



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    (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss <t>Axiovert</t> <t>200M</t> <t>Fluorescence</t> Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.
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    (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss <t>Axiovert</t> <t>200M</t> <t>Fluorescence</t> Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.
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    (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss <t>Axiovert</t> <t>200M</t> <t>Fluorescence</t> Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.
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    Image Search Results


    (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss Axiovert 200M Fluorescence Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.

    Journal: Nanotheranostics

    Article Title: Therapeutic Potential of Feline Adipose-Derived Stem Cell Exosomes in the Treatment of Feline Idiopathic Cystitis: A Characterization and Functional Analysis of miRNA Content

    doi: 10.7150/ntno.99383

    Figure Lengend Snippet: (a) fADSCs observation: fADSCs showed their typical elongated morphology. Picture was captured using 4x objective of EVOS™ XL Core Imaging System. (b) Internalization of fADSCs-derived exosomes by fADSCs. Stained exosomes with PKH26 were internalized by fADSCs and are visible as red spots inside cytoplasmic region of cells (white circles). Zeiss Axiovert 200M Fluorescence Microscope was used to capture the images (63x oil objective). Nuclei of the cells are labeledin blue; Actine filaments are stained in green.

    Article Snippet: At the end, all images were acquired using Zeiss Axiovert 200M Fluorescence Micro-scope (Zeiss, Oberkochen, Germany) equipped with a 63x oil objective.

    Techniques: Imaging, Derivative Assay, Staining, Fluorescence, Microscopy