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inverted axioobserver colibri fluorescent microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss inverted axioobserver colibri fluorescent microscope
    Inverted Axioobserver Colibri Fluorescent 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/axioobserver+fluorescence+microscope/colibri+microscope/pm40619066-232-5-4
    Average 90 stars, based on 1 article reviews
    inverted axioobserver colibri fluorescent microscope - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Fluorescence:

    Article Title: Posterior Limbal Mesenchymal Stromal Cells Promote Proliferation and Stemness of Transition Zone Cells: A Novel Insight Into Corneal Endothelial Rejuvenation.
    Article Snippet: The nuclei were labeled by DAPI, and the slides were mounted with Citifluor antifadent solution (Electron Microscopy Sciences, Hatfield, PA, USA). .. Images were taken under a Zeiss Colibri 7 fluorescence microscope. ..

    Microscopy:

    Article Title: Posterior Limbal Mesenchymal Stromal Cells Promote Proliferation and Stemness of Transition Zone Cells: A Novel Insight Into Corneal Endothelial Rejuvenation.
    Article Snippet: The nuclei were labeled by DAPI, and the slides were mounted with Citifluor antifadent solution (Electron Microscopy Sciences, Hatfield, PA, USA). .. Images were taken under a Zeiss Colibri 7 fluorescence microscope. ..

    Article Title: The Role of Complement Activation in IgM M-Protein–Associated Neuropathies
    Article Snippet: .. We analyzed the slides using a Zeiss Z1 microscope with Colibri LEDs with the following settings: ×20 magnification, ;1.75 V, 10 ms transmitted light differential interference contrast, 25% LED, 100 ms for the allophycocyanin channel. ..

    Article Title: PRIMDEx: Prototyping Rapid Innovation of Microfluidics Devices for Experimentation.
    Article Snippet: .. Micrographs taken with a Zeiss inverted AxioObserver Colibri fluorescent microscope to demonstrate image clarity and fluorescent intensity when imaging through a commercial MFD (used as a positive control) when compared to a PRIMDEx MFD (test sample). b) The graphical analysis of mean fluorescent intensity of the commercial MFD when compared to the PRIMDEx MFD demonstrating comparable functionality when used for fluorescent assays. c) The graphical analysis of mean fluorescent intensity of the MFDs at various injection parameters along the tested parameter array. ..

    other:

    Article Title: Development of the First Shuttle Vector System and Optimization of Transformation in Selenomonas sputigena .
    Article Snippet: Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea Institute of Endemic Diseases, Seoul National University Medical Research Center, Seoul 03080, Republic of Korea Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, Republic of Korea Integrated Biomedical and Life Science, Graduate School, Korea University, Seoul 02841, Republic of Korea School of Biosystems and Biomedical Sciences, Korea University, Seoul 02841, Republic of Korea

    Article Title: The effect of nanoceria on the alginate-gum arabic crosslinking mechanism and in vitro behavior as a wound dressing.
    Article Snippet: Medical practice has proven that chronic wounds can be treated successfully if the dressing is chosen according to the healing phase of the wound.. Correct intervention from the hemostasis and inflammatory phase can prevent oxidative stress and ensure optimal conditions for healing.. It is important to design a new wound dressing that does not cause additional injury, has an antioxidant effect, removes dead cells, and promotes wound healing.

    Article Title: Propylene glycol alginate sodium sulfate suppressed lung metastasis by blocking P-selectin to recruit CD4 regulatory T cells.
    Article Snippet: P-selectin has been shown to enhance growth and metastasis of mouse tumors by promoting regulatory T cell (Treg) infiltration into the tumors.. Theoretically, a P-selectin antagonist could suppress the process.. Popylene glycol alginate sodium sulfate (PSS) is a heparin-like marine drug, which was originally approved to treat cardiovascular disease in China.

    Article Title: Astrocytes and the tumor microenvironment inflammatory state dictate the killing of glioblastoma cells by Smac mimetic compounds.
    Article Snippet: Slides were mounted and IHC images acquired using Zeiss AxioImager Z2 widefield microscope with Colibri 5/7 and Apotome at 10x.

    Inverted Epifluorescence:

    Article Title: Correlation between evoked neurotransmitter release and adaptive functions in SYT1-associated neurodevelopmental disorder.
    Article Snippet: Coverslips were then rinsed twice in fresh double-distilled H2O, then mounted on glass slides using Dako Mounting Medium. .. Fixed, immunolabelled cells or live neuronal cultures were imaged on a Zeiss Axio Observer 7 inverted epifluorescence microscope with a Colibri 7 LED light source. ..

    Imaging:

    Article Title: PRIMDEx: Prototyping Rapid Innovation of Microfluidics Devices for Experimentation.
    Article Snippet: .. Micrographs taken with a Zeiss inverted AxioObserver Colibri fluorescent microscope to demonstrate image clarity and fluorescent intensity when imaging through a commercial MFD (used as a positive control) when compared to a PRIMDEx MFD (test sample). b) The graphical analysis of mean fluorescent intensity of the commercial MFD when compared to the PRIMDEx MFD demonstrating comparable functionality when used for fluorescent assays. c) The graphical analysis of mean fluorescent intensity of the MFDs at various injection parameters along the tested parameter array. ..

    Positive Control:

    Article Title: PRIMDEx: Prototyping Rapid Innovation of Microfluidics Devices for Experimentation.
    Article Snippet: .. Micrographs taken with a Zeiss inverted AxioObserver Colibri fluorescent microscope to demonstrate image clarity and fluorescent intensity when imaging through a commercial MFD (used as a positive control) when compared to a PRIMDEx MFD (test sample). b) The graphical analysis of mean fluorescent intensity of the commercial MFD when compared to the PRIMDEx MFD demonstrating comparable functionality when used for fluorescent assays. c) The graphical analysis of mean fluorescent intensity of the MFDs at various injection parameters along the tested parameter array. ..

    Injection:

    Article Title: PRIMDEx: Prototyping Rapid Innovation of Microfluidics Devices for Experimentation.
    Article Snippet: .. Micrographs taken with a Zeiss inverted AxioObserver Colibri fluorescent microscope to demonstrate image clarity and fluorescent intensity when imaging through a commercial MFD (used as a positive control) when compared to a PRIMDEx MFD (test sample). b) The graphical analysis of mean fluorescent intensity of the commercial MFD when compared to the PRIMDEx MFD demonstrating comparable functionality when used for fluorescent assays. c) The graphical analysis of mean fluorescent intensity of the MFDs at various injection parameters along the tested parameter array. ..



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    Carl Zeiss axioobserver d1 fluorescence microscope
    (A) Hippocampal neurons from ZH3 (Prnp -/- ) mice were transduced at DIV6 with a lentivirus encoding eGFP under control of the synapsin promoter to achieve neuron-specific expression. Cultures were then imaged on DIV21 using the EVOS Live Cell Imaging <t>Microscope</t> with transillumination ( Trans ) or <t>fluorescence</t> illumination ( GFP ). Merge shows a superposition of the two images. (B) Prnp -/- neurons were untransduced, or were transduced with lentiviruses encoding WT, G126V, or V208M PrP. Cells were fixed and stained with Alexa488-phalloidin (green) to visualize F-actin in dendritic spines and with D18 antibody (red) to detect PrP. Neurons from ZH3 (Prnp -/- ) and C57BL/6 (Prnp +/+ ) mice were used as negative and positive controls, respectively. Scale bar = 20 µm. (C) Higher magnification images of neurons showing dendritic shafts with protruding spines. Scale bar = 5 µm. (D) Dendritic spines of 12-15 neurons (each having 3-5 dendrites/neuron) from 2 independent experiments were counted in randomly selected areas, and statistical comparisons made using a one-way ANOVA multiple comparison test. Spine number is expressed per µm length of dendrite. Prnp -/- vs WT, p=0.4802; Prnp -/- vs G126V, p=0.9493; Prnp -/- vs V208M, p=0.2103. ns = not significant.
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    Carl Zeiss inverted axioobserver colibri fluorescent microscope
    (A) Hippocampal neurons from ZH3 (Prnp -/- ) mice were transduced at DIV6 with a lentivirus encoding eGFP under control of the synapsin promoter to achieve neuron-specific expression. Cultures were then imaged on DIV21 using the EVOS Live Cell Imaging <t>Microscope</t> with transillumination ( Trans ) or <t>fluorescence</t> illumination ( GFP ). Merge shows a superposition of the two images. (B) Prnp -/- neurons were untransduced, or were transduced with lentiviruses encoding WT, G126V, or V208M PrP. Cells were fixed and stained with Alexa488-phalloidin (green) to visualize F-actin in dendritic spines and with D18 antibody (red) to detect PrP. Neurons from ZH3 (Prnp -/- ) and C57BL/6 (Prnp +/+ ) mice were used as negative and positive controls, respectively. Scale bar = 20 µm. (C) Higher magnification images of neurons showing dendritic shafts with protruding spines. Scale bar = 5 µm. (D) Dendritic spines of 12-15 neurons (each having 3-5 dendrites/neuron) from 2 independent experiments were counted in randomly selected areas, and statistical comparisons made using a one-way ANOVA multiple comparison test. Spine number is expressed per µm length of dendrite. Prnp -/- vs WT, p=0.4802; Prnp -/- vs G126V, p=0.9493; Prnp -/- vs V208M, p=0.2103. ns = not significant.
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    Average 90 stars, based on 1 article reviews
    inverted axioobserver colibri fluorescent microscope - by Bioz Stars, 2026-10
    90/100 stars
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    Image Search Results


    (A) Hippocampal neurons from ZH3 (Prnp -/- ) mice were transduced at DIV6 with a lentivirus encoding eGFP under control of the synapsin promoter to achieve neuron-specific expression. Cultures were then imaged on DIV21 using the EVOS Live Cell Imaging Microscope with transillumination ( Trans ) or fluorescence illumination ( GFP ). Merge shows a superposition of the two images. (B) Prnp -/- neurons were untransduced, or were transduced with lentiviruses encoding WT, G126V, or V208M PrP. Cells were fixed and stained with Alexa488-phalloidin (green) to visualize F-actin in dendritic spines and with D18 antibody (red) to detect PrP. Neurons from ZH3 (Prnp -/- ) and C57BL/6 (Prnp +/+ ) mice were used as negative and positive controls, respectively. Scale bar = 20 µm. (C) Higher magnification images of neurons showing dendritic shafts with protruding spines. Scale bar = 5 µm. (D) Dendritic spines of 12-15 neurons (each having 3-5 dendrites/neuron) from 2 independent experiments were counted in randomly selected areas, and statistical comparisons made using a one-way ANOVA multiple comparison test. Spine number is expressed per µm length of dendrite. Prnp -/- vs WT, p=0.4802; Prnp -/- vs G126V, p=0.9493; Prnp -/- vs V208M, p=0.2103. ns = not significant.

    Journal: bioRxiv

    Article Title: Membrane-anchored PrP Sc is the trigger for prion synaptotoxicity

    doi: 10.1101/2025.07.11.664221

    Figure Lengend Snippet: (A) Hippocampal neurons from ZH3 (Prnp -/- ) mice were transduced at DIV6 with a lentivirus encoding eGFP under control of the synapsin promoter to achieve neuron-specific expression. Cultures were then imaged on DIV21 using the EVOS Live Cell Imaging Microscope with transillumination ( Trans ) or fluorescence illumination ( GFP ). Merge shows a superposition of the two images. (B) Prnp -/- neurons were untransduced, or were transduced with lentiviruses encoding WT, G126V, or V208M PrP. Cells were fixed and stained with Alexa488-phalloidin (green) to visualize F-actin in dendritic spines and with D18 antibody (red) to detect PrP. Neurons from ZH3 (Prnp -/- ) and C57BL/6 (Prnp +/+ ) mice were used as negative and positive controls, respectively. Scale bar = 20 µm. (C) Higher magnification images of neurons showing dendritic shafts with protruding spines. Scale bar = 5 µm. (D) Dendritic spines of 12-15 neurons (each having 3-5 dendrites/neuron) from 2 independent experiments were counted in randomly selected areas, and statistical comparisons made using a one-way ANOVA multiple comparison test. Spine number is expressed per µm length of dendrite. Prnp -/- vs WT, p=0.4802; Prnp -/- vs G126V, p=0.9493; Prnp -/- vs V208M, p=0.2103. ns = not significant.

    Article Snippet: 10-15 neurons were randomly selected and imaged using a Zeiss AxioObserver D1 Fluorescence Microscope and/or a Zeiss LSM 700 Laser Scanning Confocal Microscope with 63X oil objectives.

    Techniques: Control, Expressing, Live Cell Imaging, Microscopy, Fluorescence, Transduction, Staining, Comparison