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inverted microscope nikon eclipse te2000–5  (Nikon)


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    Structured Review

    Nikon inverted microscope nikon eclipse te2000–5
    Inverted Microscope Nikon Eclipse Te2000–5, supplied by Nikon, 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+microscope+nikon+eclipse+te2000%E2%80%935/pmc11587867-90-2-3
    Average 90 stars, based on 1 article reviews
    inverted microscope nikon eclipse te2000–5 - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Inverted Microscopy:

    Article Title: The role of clonal communication and heterogeneity in breast cancer
    Article Snippet: Sphere invasion was analyzed by measuring the invaded area at 24 and 48 h using the inverted microscope NIKON Eclipse TE2000–5 and ImageJ software.

    Article Title: Scaling of deterministic lateral displacement devices to a single column of bumping obstacles
    Article Snippet: An inverted microscope (Nikon Eclipse TE2000–5) was used to image the movement of particles and flow pattern within the device, with a blue-LED light (as the excitation source) with a fluorescence filter set (FITC, 467–498 nm excitation, 513–556 nm emission).

    Article Title: Human adipose tissue mesenchymal stem cells as a novel treatment modality for correcting obesity induced metabolic dysregulation.
    Article Snippet: Objective Obesity induced metabolic dysregulation results in cluster of chronic conditions mainly hyperglycemia, hyperinsulinemia, dyslipidemia, diabetes, cardiovascular complications and insulin resistance.. To investigate the effect of i.m. injection of human adipose tissue derived mesenchymal stem cells and its secretome in correcting obesity induced metabolic dysregulation in high fat diet fed obese model of mice and understand its mechanism of action.. Subjects We injected human adipose tissue derived mesenchymal stem cells (ADMSCs) suspension (CS), conditioned medium (CM) and the cell lysate (CL) intramuscularly in high fat diet (HFD)-induced C57BL/6 mice.

    Fluorescence:

    Article Title: The role of clonal communication and heterogeneity in breast cancer
    Article Snippet: Sphere invasion was analyzed by measuring the invaded area at 24 and 48 h using the inverted microscope NIKON Eclipse TE2000–5 and ImageJ software.

    Article Title: Scaling of deterministic lateral displacement devices to a single column of bumping obstacles
    Article Snippet: An inverted microscope (Nikon Eclipse TE2000–5) was used to image the movement of particles and flow pattern within the device, with a blue-LED light (as the excitation source) with a fluorescence filter set (FITC, 467–498 nm excitation, 513–556 nm emission).

    Article Title: Human adipose tissue mesenchymal stem cells as a novel treatment modality for correcting obesity induced metabolic dysregulation.
    Article Snippet: Objective Obesity induced metabolic dysregulation results in cluster of chronic conditions mainly hyperglycemia, hyperinsulinemia, dyslipidemia, diabetes, cardiovascular complications and insulin resistance.. To investigate the effect of i.m. injection of human adipose tissue derived mesenchymal stem cells and its secretome in correcting obesity induced metabolic dysregulation in high fat diet fed obese model of mice and understand its mechanism of action.. Subjects We injected human adipose tissue derived mesenchymal stem cells (ADMSCs) suspension (CS), conditioned medium (CM) and the cell lysate (CL) intramuscularly in high fat diet (HFD)-induced C57BL/6 mice.

    Software:

    Article Title: The role of clonal communication and heterogeneity in breast cancer
    Article Snippet: Sphere invasion was analyzed by measuring the invaded area at 24 and 48 h using the inverted microscope NIKON Eclipse TE2000–5 and ImageJ software.

    Article Title: Scaling of deterministic lateral displacement devices to a single column of bumping obstacles
    Article Snippet: An inverted microscope (Nikon Eclipse TE2000–5) was used to image the movement of particles and flow pattern within the device, with a blue-LED light (as the excitation source) with a fluorescence filter set (FITC, 467–498 nm excitation, 513–556 nm emission).

    Article Title: Human adipose tissue mesenchymal stem cells as a novel treatment modality for correcting obesity induced metabolic dysregulation.
    Article Snippet: Objective Obesity induced metabolic dysregulation results in cluster of chronic conditions mainly hyperglycemia, hyperinsulinemia, dyslipidemia, diabetes, cardiovascular complications and insulin resistance.. To investigate the effect of i.m. injection of human adipose tissue derived mesenchymal stem cells and its secretome in correcting obesity induced metabolic dysregulation in high fat diet fed obese model of mice and understand its mechanism of action.. Subjects We injected human adipose tissue derived mesenchymal stem cells (ADMSCs) suspension (CS), conditioned medium (CM) and the cell lysate (CL) intramuscularly in high fat diet (HFD)-induced C57BL/6 mice.



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    Nikon inverted uv microscope nikon eclipse te2000-5 microscope coupled with a nikon hb-10101af super high-pressure mercury lamp
    H protein production and trafficking is inhibited in PPRV-infected BST2-overexpressing cells. PPRV H distribution is modified in BST2-transfected infected cells. ( A ) Vero cSLAM cells were transfected with plasmids expressing the indicated BST2 protein (or mock transfected) before being infected with PPRV Tu00 at an MOI of 0.1. Cells were fixed at 16 h post infection before staining with relevant antibodies (PPRV H, red and BST2, green). Micrographs were taken on a Leica confocal <t>microscope</t> with line of interest analysis of colocalization performed using the inbuilt software. The white boxed insets in the merged panels reflect the region chosen for analysis in the “zoom” panel (right), with the x-axis on the colocalization graphs representing the 15 µm white lines indicated on the adjacent zoomed images. ( B ) A zoomed image of a single large BST2-expressing syncytia indicating the approximate position of the plasma membrane.
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    Image Search Results


    H protein production and trafficking is inhibited in PPRV-infected BST2-overexpressing cells. PPRV H distribution is modified in BST2-transfected infected cells. ( A ) Vero cSLAM cells were transfected with plasmids expressing the indicated BST2 protein (or mock transfected) before being infected with PPRV Tu00 at an MOI of 0.1. Cells were fixed at 16 h post infection before staining with relevant antibodies (PPRV H, red and BST2, green). Micrographs were taken on a Leica confocal microscope with line of interest analysis of colocalization performed using the inbuilt software. The white boxed insets in the merged panels reflect the region chosen for analysis in the “zoom” panel (right), with the x-axis on the colocalization graphs representing the 15 µm white lines indicated on the adjacent zoomed images. ( B ) A zoomed image of a single large BST2-expressing syncytia indicating the approximate position of the plasma membrane.

    Journal: Viruses

    Article Title: BST2/Tetherin Overexpression Modulates Morbillivirus Glycoprotein Production to Inhibit Cell–Cell Fusion

    doi: 10.3390/v11080692

    Figure Lengend Snippet: H protein production and trafficking is inhibited in PPRV-infected BST2-overexpressing cells. PPRV H distribution is modified in BST2-transfected infected cells. ( A ) Vero cSLAM cells were transfected with plasmids expressing the indicated BST2 protein (or mock transfected) before being infected with PPRV Tu00 at an MOI of 0.1. Cells were fixed at 16 h post infection before staining with relevant antibodies (PPRV H, red and BST2, green). Micrographs were taken on a Leica confocal microscope with line of interest analysis of colocalization performed using the inbuilt software. The white boxed insets in the merged panels reflect the region chosen for analysis in the “zoom” panel (right), with the x-axis on the colocalization graphs representing the 15 µm white lines indicated on the adjacent zoomed images. ( B ) A zoomed image of a single large BST2-expressing syncytia indicating the approximate position of the plasma membrane.

    Article Snippet: For phase-contrast microscopy, MeV-GFP infected cells were visualized by phase-contrast microscopy using an inverted UV microscope (Nikon Eclipse TE2000-5 microscope coupled with a Nikon HB-10101AF super high-pressure mercury lamp) equipped with a Hamamatsu C472-95 digital camera (Sony, Minato-ku, Japan).

    Techniques: Infection, Modification, Transfection, Expressing, Staining, Microscopy, Software, Clinical Proteomics, Membrane