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zeiss axioobserver z1  (Carl Zeiss)


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    Carl Zeiss zeiss axioobserver z1
    Figure 1. Matrigel Branching Assays using Endometrial Tissue Conditioned Media. A, B, and C: Media only control. Cells treated with conditioned media endometrium supplying the closest to mean litter weight fetus (CTMLW) (D, E, and F) and lightest fetus (G, H, and I) at gestational day (GD) 45. Cells treated with conditioned media from endometrium supplying the CTMLW (J, K, and L) or lightest fetus (M, N, and O) at GD60. All conditioned media collected after 18 hours of tissue explant culture. The CTMLW and lightest fetuses within GD were from the same litter. Scale bars represent 10 μM. Representative images taken using the Zeiss <t>AxioObserver</t> <t>Z1</t> at ×5 magnification at 2, 6, and 10 hours post-seeding of the endothelial cells.
    Zeiss Axioobserver Z1, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 571 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/axioobserver+d1+microscope/pm31093645-168-5-5?v=Carl+Zeiss
    Average 97 stars, based on 571 article reviews
    zeiss axioobserver z1 - by Bioz Stars, 2026-08
    97/100 stars

    Images

    1) Product Images from "Novel relationships between porcine fetal size, sex, and endometrial angiogenesis†."

    Article Title: Novel relationships between porcine fetal size, sex, and endometrial angiogenesis†.

    Journal: Biology of reproduction

    doi: 10.1093/biolre/ioz068

    Figure 1. Matrigel Branching Assays using Endometrial Tissue Conditioned Media. A, B, and C: Media only control. Cells treated with conditioned media endometrium supplying the closest to mean litter weight fetus (CTMLW) (D, E, and F) and lightest fetus (G, H, and I) at gestational day (GD) 45. Cells treated with conditioned media from endometrium supplying the CTMLW (J, K, and L) or lightest fetus (M, N, and O) at GD60. All conditioned media collected after 18 hours of tissue explant culture. The CTMLW and lightest fetuses within GD were from the same litter. Scale bars represent 10 μM. Representative images taken using the Zeiss AxioObserver Z1 at ×5 magnification at 2, 6, and 10 hours post-seeding of the endothelial cells.
    Figure Legend Snippet: Figure 1. Matrigel Branching Assays using Endometrial Tissue Conditioned Media. A, B, and C: Media only control. Cells treated with conditioned media endometrium supplying the closest to mean litter weight fetus (CTMLW) (D, E, and F) and lightest fetus (G, H, and I) at gestational day (GD) 45. Cells treated with conditioned media from endometrium supplying the CTMLW (J, K, and L) or lightest fetus (M, N, and O) at GD60. All conditioned media collected after 18 hours of tissue explant culture. The CTMLW and lightest fetuses within GD were from the same litter. Scale bars represent 10 μM. Representative images taken using the Zeiss AxioObserver Z1 at ×5 magnification at 2, 6, and 10 hours post-seeding of the endothelial cells.

    Techniques Used: Control



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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