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eclipse te300 inverted fluorescence phase contrast microscope  (Nikon)


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    Structured Review

    Nikon eclipse te300 inverted fluorescence phase contrast microscope
    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse <t>TE300</t> Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
    Eclipse Te300 Inverted Fluorescence Phase Contrast Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59714 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/inverted+microscope+eclipse+te300/Objectives/pmc12811465-194-7-6
    Average 99 stars, based on 59714 article reviews
    eclipse te300 inverted fluorescence phase contrast microscope - by Bioz Stars, 2026-09
    99/100 stars

    Images

    1) Product Images from "Comparative analysis of Borrelia’s Defence mechanisms and their impact on genetic manipulation of low-passage isolates of Borrelia afzelii and Borrelia garinii"

    Article Title: Comparative analysis of Borrelia’s Defence mechanisms and their impact on genetic manipulation of low-passage isolates of Borrelia afzelii and Borrelia garinii

    Journal: Current Research in Microbial Sciences

    doi: 10.1016/j.crmicr.2025.100543

    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
    Figure Legend Snippet: Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.

    Techniques Used: Fluorescence, Transformation Assay, Plasmid Preparation, In Vitro, Methylation, Modification, Microscopy

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    Article Title: Identification of TSSK1 and TSSK2 as Novel Targets for Male Contraception
    Article Snippet: The slides were imaged on an inverted microscope (Eclipse TE300; Nikon) with epifluorescence and DIC images were taken with a 60x PlanApo/DIC objective (NA 1.49; Nikon).

    Article Title: The pair ceramide 1-phosphate/ceramide kinase regulates intracellular calcium and progesterone-induced human sperm acrosomal exocytosis.
    Article Snippet: Male gametes were immobilized on poly-L-lysine-coated coverslips, mounted on a chamber, and placed on the stage of an inverted microscope (Eclipse TE300 Nikon).

    Article Title: H3.1/3.2 regulate the initial progression of the gene expression program.
    Article Snippet: Microinjection was performed using an inverted microscope (Eclipse TE300, Nikon, Tokyo, Japan), a micromanipulator (MO-202U, Narishige, Tokyo, Japan), and a microinjector (IM300, Narishige).

    Article Title: Development of a Water-Soluble Nanomicellar Formulation Loaded with Trans-Resveratrol Using Polyethylene Glycol Monostearate for the Treatment of Intracerebral Hemorrhage
    Article Snippet: Bright-field images were captured randomly using an inverted microscope (ECLIPSE TE300; Nikon, Tokyo, Japan) with a camera (DS-Ri2; Nikon).

    Article Title: Identification of TSSK1 and TSSK2 as Novel Targets for Male Contraception
    Article Snippet: The slides were imaged on an inverted microscope (Eclipse TE300; Nikon, Melville, NY, USA) with a 40× objective (NA 1.49; Nikon).

    Article Title: Stress response mechanisms in protein misfolding diseases: Profiling a cellular model of Huntington's disease.
    Article Snippet: Cells were live imaged in a customised Nikon-Prior-Hamamatsu (NPH) Imaging System, composed by an inverted microscope (Eclipse TE300, Nikon), a motorized stage (ProScan, Prior), a CCD camera (ORCA-ER, Hamamatsu), and a monochromator (Polychrome II, Photonics), all controlled by the open-source software Micro-Manager (v. 2.0; https://micro-manager.org).

    Inverted Microscopy:

    Article Title: Resolvin E1 attenuates doxorubicin-induced endothelial senescence by modulating NLRP3 inflammasome activation.
    Article Snippet: Endothelial cell senescence contributes to chronic inflammation and endothelial dysfunction, while favoring cardiovascular disorders and frailty.. Senescent cells acquire a pro-inflammatory secretory phenotype that further propagates inflammation and senescence to neighboring cells.. Cell senescence can be provoked by plethora of stressors, including inflammatory molecules and chemotherapeutic drugs.

    Article Title: DPP4 Promotes Human Endothelial Cell Senescence and Dysfunction via the PAR2–COX-2–TP Axis and NLRP3 Inflammasome Activation
    Article Snippet: .. ASC specks per field were quantified by manual blind scoring of 17 radial distributed fields in each sample, under an inverted microscope Eclipse TE300 (Nikon). .. Representative images were acquired with a TCS SPE confocal microscope (Leica, Wetzlar, Germany).



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    Nikon eclipse te300 inverted fluorescence phase contrast microscope
    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse <t>TE300</t> Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
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    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse <t>TE300</t> Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
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    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse <t>TE300</t> Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
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    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse <t>TE300</t> Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
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    Image Search Results


    Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.

    Journal: Current Research in Microbial Sciences

    Article Title: Comparative analysis of Borrelia’s Defence mechanisms and their impact on genetic manipulation of low-passage isolates of Borrelia afzelii and Borrelia garinii

    doi: 10.1016/j.crmicr.2025.100543

    Figure Lengend Snippet: Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.

    Article Snippet: All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.

    Techniques: Fluorescence, Transformation Assay, Plasmid Preparation, In Vitro, Methylation, Modification, Microscopy