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microscope equipped with an image analyzer zen 2 blue edition  (Carl Zeiss)


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    Structured Review

    Carl Zeiss microscope equipped with an image analyzer zen 2 blue edition
    Microscope Equipped With An Image Analyzer Zen 2 Blue Edition, 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/image+analyzer+2+microscope/analyzer+image/pmc07425232-68-19-29
    Average 90 stars, based on 1 article reviews
    microscope equipped with an image analyzer zen 2 blue edition - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Tomography:

    Article Title: Clinical Outcomes of XEN45 Gel Stent Implantation ( Ab Externo , Open Conjunctival Approach) versus Trabeculectomy: A Real-World Study
    Article Snippet: .. Biometric assessments were performed using a swept-source optical coherence tomography–based optical biometer (IOL Master-700, Carl Zeiss Meditec), and Humphrey field analyzer was used for detecting information of monocular visual field. ..

    Microscopy:

    Article Title: Neural Markers Predict Tendon Healing Outcomes in an Ovine Achilles Tendon Injury Model: Spontaneous Repair Versus Amniotic Epithelial Cell-Induced Regeneration.
    Article Snippet: Moreover, quantitative analyses were carried on immunohistochemical images to measure cell alignment and angle deviation, tendon morphometric parameters that indirectly indicate ECM organization [14,56], using the directionality plugin in ImageJ 1.53 k (NIH, Bethesda, MD, USA) software to assess the extent of tissue reorganization, as detailed in a previously published report [14,56]. .. Cell alignment analyses were performed with an Axioscop 2plus epifluorescence microscope (Zeiss, Oberkochen, Germany) equipped with a cooled color charge-coupled device camera (CCD; Axiovision Cam, Zeiss) interfaced with an interactive and automatic image analyzer (Axiovision, Zeiss) at 20× magnification by acquiring 5 randomly selected fields from each area, starting from area 1 and continuing throughout the repairing areas (areas 2 and 3). ..

    Article Title: Diversity and biological activities of endophytic fungi: insights from in-silico docking studies.
    Article Snippet: A study was conducted to understand the diversity of endophytic fungi from various natural hosts and their antimicrobial and alkali-tolerance activity with bioactive metabolite profiling and in-silico docking.. A total of 176 endophytic fungi were isolated from nine hosts from India, and classified into 31 genera based on their morphology and molecular analysis of the ITS rDNA gene region.. The endophytic community was dominated by fungi belonging to the genus Colletotrichum (20.5%), followed by Nigrospora (14.03%), Pestalotiopsis (9.35%), Lasiodiplodia (8.2%) and lastly by Hypoxylon (7.01%).

    Article Title: Discovery of Alanomyces manoharacharyi : A Novel Fungus Identified Using Genome Sequencing and Metabolomic Analysis.
    Article Snippet: .. Microscopic structures of the isolates were recorded from pure culture using a staining cum-mounting medium, lactophenol cotton blue, under a Carl Zeiss Image Analyzer 2 (Oberkochen, Germany) microscope. .. Measurements and photomicrographs of the fungal structures were recorded using Axiovision Rel 4.8 software and Digi-Cam attached with the Carl Zeiss Image Analyzer 2 microscope.

    Software:

    Article Title: Analysis of Mechanoreceptors and Free Nerve Endings in the Lateral Collateral Ligament of the Elbow Using Immunofluorescence and Confocal Microscopy.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Article Title: A new target for drug repositioning: CEBPα elicits LL-37 expression in a vitamin D-independent manner promoting Mtb clearance.
    Article Snippet: Tuberculosis is an infectious disease caused by Mycobacterium tuberculosis (Mtb) and is a growing public health problem worldwide.. Within the innate immune response, we highlight the secretion of the antimicrobial peptide LL-37, which is crucial for Mtb elimination in infected cells.. Previous reports have shown that CEBPα activation induces LL-37 independently of its main inducer, vitamin D, under endoplasmic reticulum (ER) stress.

    Article Title: Structural and Distribution Analysis of Mechanoreceptors and Free Nerve Endings in the Annular Pulleys of the Flexor Tendons of the Hand.
    Article Snippet: Background: The hand is essential in enabling physical interaction with the environment, with the annular pulleys playing a key role in its functionality.. These fibrocartilaginous structures, located along the flexor tendons, are vascularized and may contain nerve endings and mechanoreceptors, aligning tendons with the bones to optimize finger flexion.. However, their innervation remains poorly understood, limiting therapeutic advancements for flexor tendon conditions, such as stenosing tenosynovitis (trigger finger).

    Staining:

    Article Title: Discovery of Alanomyces manoharacharyi : A Novel Fungus Identified Using Genome Sequencing and Metabolomic Analysis.
    Article Snippet: .. Microscopic structures of the isolates were recorded from pure culture using a staining cum-mounting medium, lactophenol cotton blue, under a Carl Zeiss Image Analyzer 2 (Oberkochen, Germany) microscope. .. Measurements and photomicrographs of the fungal structures were recorded using Axiovision Rel 4.8 software and Digi-Cam attached with the Carl Zeiss Image Analyzer 2 microscope.



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    (A) Isolation from liposuction sample. (B) Upper and lower left, ASCs and mature differentiated adipocytes, both stained with red oil (×100): upper left figure shows ASCs stained, negative for red oil test, and adherent in plasticware plate; lower left shows mature differentiated adipocytes stained, positive for red oil test, and adherent in plasticware plate. (B) Upper and lower right, differential interference contrast (DIC-Nomarski) combined with DAPI (×400) for ASCs and mature differentiated adipocytes is shown. (C) Mature differentiated adipocytes with red oil staining (magnification at ×100, ×200, ×400, and ×630, scale bar = 40 μm) are shown. Axioskop-2-Zeiss <t>microscope.</t>
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    Carl Zeiss microscope equipped with an image analyzer zen 2 blue edition
    (A) Isolation from liposuction sample. (B) Upper and lower left, ASCs and mature differentiated adipocytes, both stained with red oil (×100): upper left figure shows ASCs stained, negative for red oil test, and adherent in plasticware plate; lower left shows mature differentiated adipocytes stained, positive for red oil test, and adherent in plasticware plate. (B) Upper and lower right, differential interference contrast (DIC-Nomarski) combined with DAPI (×400) for ASCs and mature differentiated adipocytes is shown. (C) Mature differentiated adipocytes with red oil staining (magnification at ×100, ×200, ×400, and ×630, scale bar = 40 μm) are shown. Axioskop-2-Zeiss <t>microscope.</t>
    Microscope Equipped With An Image Analyzer Zen 2 Blue Edition, 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/image+analyzer+2+microscope/analyzer+image/pmc07425232-68-19-29
    Average 90 stars, based on 1 article reviews
    microscope equipped with an image analyzer zen 2 blue edition - by Bioz Stars, 2026-10
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    Image Search Results


    (A) Isolation from liposuction sample. (B) Upper and lower left, ASCs and mature differentiated adipocytes, both stained with red oil (×100): upper left figure shows ASCs stained, negative for red oil test, and adherent in plasticware plate; lower left shows mature differentiated adipocytes stained, positive for red oil test, and adherent in plasticware plate. (B) Upper and lower right, differential interference contrast (DIC-Nomarski) combined with DAPI (×400) for ASCs and mature differentiated adipocytes is shown. (C) Mature differentiated adipocytes with red oil staining (magnification at ×100, ×200, ×400, and ×630, scale bar = 40 μm) are shown. Axioskop-2-Zeiss microscope.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Leptin and TGF-β1 Downregulate PREP1 Expression in Human Adipose-Derived Mesenchymal Stem Cells and Mature Adipocytes

    doi: 10.3389/fcell.2021.700481

    Figure Lengend Snippet: (A) Isolation from liposuction sample. (B) Upper and lower left, ASCs and mature differentiated adipocytes, both stained with red oil (×100): upper left figure shows ASCs stained, negative for red oil test, and adherent in plasticware plate; lower left shows mature differentiated adipocytes stained, positive for red oil test, and adherent in plasticware plate. (B) Upper and lower right, differential interference contrast (DIC-Nomarski) combined with DAPI (×400) for ASCs and mature differentiated adipocytes is shown. (C) Mature differentiated adipocytes with red oil staining (magnification at ×100, ×200, ×400, and ×630, scale bar = 40 μm) are shown. Axioskop-2-Zeiss microscope.

    Article Snippet: The percentage of cells undergoing adipogenesis was calculated by image analyzer microscope (Axioskop-2-Zeiss, Jena, Germany).

    Techniques: Isolation, Staining, Microscopy

    (A) Flow cytometry analysis on ASCs and on mature differentiated adipocytes for antigen surface markers: the results are shown as box-plots with medians (lines inside the boxes), mature differentiated adipocytes significantly expressed CD105, CD73, and CD90 in comparison with ASCs (* p = 0.0272 for CD105, ** p < 0.0001 for CD73, and CD90; n = 3 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis in ASCs and in adipocytes. The numbers indicate the percentage of double positive cells for CD73 and CD90. (B) Representative immunofluorescence for antigen surface markers on mature differentiated adipocytes is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence; negative, CD34 (green), CD73 (red), and CD90 (green) (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Leptin and TGF-β1 Downregulate PREP1 Expression in Human Adipose-Derived Mesenchymal Stem Cells and Mature Adipocytes

    doi: 10.3389/fcell.2021.700481

    Figure Lengend Snippet: (A) Flow cytometry analysis on ASCs and on mature differentiated adipocytes for antigen surface markers: the results are shown as box-plots with medians (lines inside the boxes), mature differentiated adipocytes significantly expressed CD105, CD73, and CD90 in comparison with ASCs (* p = 0.0272 for CD105, ** p < 0.0001 for CD73, and CD90; n = 3 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis in ASCs and in adipocytes. The numbers indicate the percentage of double positive cells for CD73 and CD90. (B) Representative immunofluorescence for antigen surface markers on mature differentiated adipocytes is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence; negative, CD34 (green), CD73 (red), and CD90 (green) (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Article Snippet: The percentage of cells undergoing adipogenesis was calculated by image analyzer microscope (Axioskop-2-Zeiss, Jena, Germany).

    Techniques: Flow Cytometry, Comparison, Immunofluorescence, Fluorescence, Microscopy

    (A) Flow cytometry analysis on ASCs for PREP1: both leptin (0.05 μM) and TGF-β1 (400 nM) significantly reduced PREP1 expression (* p = 0.0149 and ** p = 0.0318, respectively); the results are shown as box-plots with medians (lines inside the boxes), 25th and 75th percentiles (limits of boxes), and the 10th and 90th percentiles (whiskers) ( n = 7 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis. The numbers indicate the percentage of positive cells for PREP1. (B) Representative immunofluorescence for PREP1 (green) on ASCs is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Leptin and TGF-β1 Downregulate PREP1 Expression in Human Adipose-Derived Mesenchymal Stem Cells and Mature Adipocytes

    doi: 10.3389/fcell.2021.700481

    Figure Lengend Snippet: (A) Flow cytometry analysis on ASCs for PREP1: both leptin (0.05 μM) and TGF-β1 (400 nM) significantly reduced PREP1 expression (* p = 0.0149 and ** p = 0.0318, respectively); the results are shown as box-plots with medians (lines inside the boxes), 25th and 75th percentiles (limits of boxes), and the 10th and 90th percentiles (whiskers) ( n = 7 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis. The numbers indicate the percentage of positive cells for PREP1. (B) Representative immunofluorescence for PREP1 (green) on ASCs is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Article Snippet: The percentage of cells undergoing adipogenesis was calculated by image analyzer microscope (Axioskop-2-Zeiss, Jena, Germany).

    Techniques: Flow Cytometry, Expressing, Immunofluorescence, Fluorescence, Microscopy

    (A) Flow cytometry analysis on mature differentiated adipocytes for PREP1: both leptin (0.05 μM) and TGF-β1 (400 nM) significantly reduced PREP1 expression (* p = 0.0138 and ** p = 0.0461, respectively); the results are shown as box-plots with medians (lines inside the boxes), 25th and 75th percentiles (limits of boxes), and the 10th and 90th percentiles (whiskers) ( n = 6 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis. The numbers indicate the percentage of positive cells for PREP1. (B) Representative immunofluorescence for PREP1 (green) on mature differentiated adipocytes is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Leptin and TGF-β1 Downregulate PREP1 Expression in Human Adipose-Derived Mesenchymal Stem Cells and Mature Adipocytes

    doi: 10.3389/fcell.2021.700481

    Figure Lengend Snippet: (A) Flow cytometry analysis on mature differentiated adipocytes for PREP1: both leptin (0.05 μM) and TGF-β1 (400 nM) significantly reduced PREP1 expression (* p = 0.0138 and ** p = 0.0461, respectively); the results are shown as box-plots with medians (lines inside the boxes), 25th and 75th percentiles (limits of boxes), and the 10th and 90th percentiles (whiskers) ( n = 6 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis. The numbers indicate the percentage of positive cells for PREP1. (B) Representative immunofluorescence for PREP1 (green) on mature differentiated adipocytes is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Article Snippet: The percentage of cells undergoing adipogenesis was calculated by image analyzer microscope (Axioskop-2-Zeiss, Jena, Germany).

    Techniques: Flow Cytometry, Expressing, Immunofluorescence, Fluorescence, Microscopy

    (A) Flow cytometry analysis on mature differentiated adipocytes for TLR4: both leptin (0.05 μM) and TGF-β1 (400 nM) significantly increased TLR4 expression (* p = 0.0178 and ** p = 0.0325, respectively); the results are shown as box-plots with medians (lines inside the boxes) ( n = 4 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis. The numbers indicate the percentage of positive cells for TLR4. (B) Representative immunofluorescence for TLR4 (red) on mature differentiated adipocytes is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Leptin and TGF-β1 Downregulate PREP1 Expression in Human Adipose-Derived Mesenchymal Stem Cells and Mature Adipocytes

    doi: 10.3389/fcell.2021.700481

    Figure Lengend Snippet: (A) Flow cytometry analysis on mature differentiated adipocytes for TLR4: both leptin (0.05 μM) and TGF-β1 (400 nM) significantly increased TLR4 expression (* p = 0.0178 and ** p = 0.0325, respectively); the results are shown as box-plots with medians (lines inside the boxes) ( n = 4 experiments). Analysis of variance (ANOVA), Fisher’s PLSD. Right, representative examples of flow cytometric analysis. The numbers indicate the percentage of positive cells for TLR4. (B) Representative immunofluorescence for TLR4 (red) on mature differentiated adipocytes is shown: higher, differential interference contrast (DIC-Nomarski) combined with DAPI and fluorescence; lower, DAPI with fluorescence (magnification at ×400, scale bar = 40 μm). Axioskop-2-Zeiss microscope.

    Article Snippet: The percentage of cells undergoing adipogenesis was calculated by image analyzer microscope (Axioskop-2-Zeiss, Jena, Germany).

    Techniques: Flow Cytometry, Expressing, Immunofluorescence, Fluorescence, Microscopy