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inverted microscope  (Nikon)


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    Structured Review

    Nikon inverted microscope
    Inverted Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 14830 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+te2000+5+microscope/Inverted+Microscopes/pmc10785265-180-6-8
    Average 99 stars, based on 14830 article reviews
    inverted microscope - by Bioz Stars, 2026-11
    99/100 stars

    Images

    Related Articles

    Immunofluorescence:

    Article Title: Fejerin promotes autophagy via the PINK1-Parkin pathway and is protective against Parkinson’s disease pathology
    Article Snippet: The subsequent day, following a PBS wash, the cells were pairedwith suitably tagged secondary antibodies(1:100, BA1127orBA1126, Boster,Wuhan, China) and kept in the dark at 37 °C for 1 h. Finally, the coverslips were secured onto glass slides using an anti-fade mounting medium laced with DAPI (Abcam, Cambridge, UK) to highlight the cell nuclei. .. Finally, immunofluorescence snapshots were taken, and fluorescence intensity was measured with both a Nikon inverted fluorescence microscope and a confocal microscope. ..

    Fluorescence:

    Article Title: Fejerin promotes autophagy via the PINK1-Parkin pathway and is protective against Parkinson’s disease pathology
    Article Snippet: The subsequent day, following a PBS wash, the cells were pairedwith suitably tagged secondary antibodies(1:100, BA1127orBA1126, Boster,Wuhan, China) and kept in the dark at 37 °C for 1 h. Finally, the coverslips were secured onto glass slides using an anti-fade mounting medium laced with DAPI (Abcam, Cambridge, UK) to highlight the cell nuclei. .. Finally, immunofluorescence snapshots were taken, and fluorescence intensity was measured with both a Nikon inverted fluorescence microscope and a confocal microscope. ..

    Article Title: 3D-printed PLCL scaffolds for breast reconstructive tissue engineering: a pre-clinical study in a rabbit model
    Article Snippet: At day 7 of differentiation, cells were labelled for 20 min at 37 °C with two fluorescent dyes, 1 μg/ml each: Hoechst 33,342 (Invitrogen—H3570; Thermofisher) and BODIPY 493/503 (Invitrogen—D3922; Thermofisher). .. Following two PBS washes, visualization and quantification were carried out by fluorescence microscopy using a Nikon Eclipse Ts2 – FL inverted microscopes (Nikon; Amstelvee, The Netherlands) with a 10 X objective and NIS-Elements software (Nikon) for image acquisition and analysis. ..

    Article Title: Mechanism of luteolin in treating chronic heart failure by regulating HIF-1 signaling pathway-mediated mitochondrial damage to inhibit cardiomyocyte apoptosis
    Article Snippet: The next day, a fluorophore-conjugated secondary antibody (Servicebio, Wuhan, China) and DAPI nuclear counterstain (Servicebio, Wuhan, China) were added sequentially in the dark. .. Fluorescence images were captured using an inverted fluorescence microscope (Nikon, Tokyo, Japan), and the mean fluorescence intensity of HIF1A was quantified among groups. .. Following fixation, permeabilization, and blocking, H9C2 cells were stained using a Toluidine Blue Staining Kit (Servicebio, Wuhan, China) ( ) and a Sirius Red Staining Kit (Servicebio, Wuhan, China) , respectively.

    Article Title: Natural product-like phenanthroquinolizidines: asymmetric synthesis and anti-glioblastoma activity evaluation.
    Article Snippet: Phenanthroquinolizidine alkaloids exhibit exceptional potency and broad-spectrum antitumor activities against various human malignancies.. Here, utilizing a ring-expansion strategy based on phenanthroindolizidines, we report the substrate-controlled asymmetric synthesis of a pair of novel enantiomeric natural product-like phenanthroquinolizidines, S-CAT6 and R-CAT6.. The synthesis employs (L)or (D)-2-aminoadipic acid dimethyl ester as the chiral pool source, streamlining the sequence through a one-pot iodination/nucleophilic substitution, followed by E-ring cyclization, Friedel-Crafts acylation for D-ring annulation, and terminal deoxygenation.

    Article Title: Mechanistic insights into ultraviolet-crosslinked sulfonated hyaluronic acid microspheres for stable biointerfaces on biodegradable cerebrovascular magnesium implants
    Article Snippet: .. Optical microscopy analysis: All samles were examined using an inverted fluorescence Optical icroscope (Nikon Ti-S, Tokyo, Japan), assessing cellular adesion patterns and morphological alteration. .. Surface topogaphy and cellular adhesion patterns were characterized by a eld-emission scanning electron microscope (FE-SEM, ZEISS IGMA 300, Germany) at an accelerating voltage of 5 kV by econdary electron detection [ 26 ].

    Article Title: M2 Macrophage-Derived Small Extracellular Vesicle miR-106a-Loaded QCG Hydrogel Targets the RNF128-LXR Pathway to Reprogram Chondrocyte Cholesterol Metabolism for Osteoarthritis Therapy.
    Article Snippet: Nuclei were counterstained with Hoechst 33342 (C1022, Beyotime, China). .. Images were acquired with an inverted fluorescence microscope (Nikon, Japan), and EdU-positive cells were quantified using ImageJ software. .. Cell senescence was evaluated using the β-Galactosidase Staining Kit (C0602, Beyotime, China).

    Microscopy:

    Article Title: Fejerin promotes autophagy via the PINK1-Parkin pathway and is protective against Parkinson’s disease pathology
    Article Snippet: The subsequent day, following a PBS wash, the cells were pairedwith suitably tagged secondary antibodies(1:100, BA1127orBA1126, Boster,Wuhan, China) and kept in the dark at 37 °C for 1 h. Finally, the coverslips were secured onto glass slides using an anti-fade mounting medium laced with DAPI (Abcam, Cambridge, UK) to highlight the cell nuclei. .. Finally, immunofluorescence snapshots were taken, and fluorescence intensity was measured with both a Nikon inverted fluorescence microscope and a confocal microscope. ..

    Article Title: 3D-printed PLCL scaffolds for breast reconstructive tissue engineering: a pre-clinical study in a rabbit model
    Article Snippet: At day 7 of differentiation, cells were labelled for 20 min at 37 °C with two fluorescent dyes, 1 μg/ml each: Hoechst 33,342 (Invitrogen—H3570; Thermofisher) and BODIPY 493/503 (Invitrogen—D3922; Thermofisher). .. Following two PBS washes, visualization and quantification were carried out by fluorescence microscopy using a Nikon Eclipse Ts2 – FL inverted microscopes (Nikon; Amstelvee, The Netherlands) with a 10 X objective and NIS-Elements software (Nikon) for image acquisition and analysis. ..

    Article Title: Mechanism of luteolin in treating chronic heart failure by regulating HIF-1 signaling pathway-mediated mitochondrial damage to inhibit cardiomyocyte apoptosis
    Article Snippet: The next day, a fluorophore-conjugated secondary antibody (Servicebio, Wuhan, China) and DAPI nuclear counterstain (Servicebio, Wuhan, China) were added sequentially in the dark. .. Fluorescence images were captured using an inverted fluorescence microscope (Nikon, Tokyo, Japan), and the mean fluorescence intensity of HIF1A was quantified among groups. .. Following fixation, permeabilization, and blocking, H9C2 cells were stained using a Toluidine Blue Staining Kit (Servicebio, Wuhan, China) ( ) and a Sirius Red Staining Kit (Servicebio, Wuhan, China) , respectively.

    Article Title: Natural product-like phenanthroquinolizidines: asymmetric synthesis and anti-glioblastoma activity evaluation.
    Article Snippet: Phenanthroquinolizidine alkaloids exhibit exceptional potency and broad-spectrum antitumor activities against various human malignancies.. Here, utilizing a ring-expansion strategy based on phenanthroindolizidines, we report the substrate-controlled asymmetric synthesis of a pair of novel enantiomeric natural product-like phenanthroquinolizidines, S-CAT6 and R-CAT6.. The synthesis employs (L)or (D)-2-aminoadipic acid dimethyl ester as the chiral pool source, streamlining the sequence through a one-pot iodination/nucleophilic substitution, followed by E-ring cyclization, Friedel-Crafts acylation for D-ring annulation, and terminal deoxygenation.

    Article Title: A smart magneto-responsive ternary 3D platform for actively steering stereoscopic infiltration and chronological osteogenic differentiation of BMSCs.
    Article Snippet: The limited effective infiltration of cells into the interior of scaffolds remains a critical bottleneck limiting the therapeutic application of bone tissue engineering.. To address this challenge, this study developed a physically self-assembled ternary smart magneto-responsive composite platform (MGO/CS) based on chitosan, graphene oxide, and superparamagnetic iron oxide nanoparticles (SPIONs).. Although the incorporation of SPIONs reduced the mean pore size of the scaffold from 306.64 ± 52.25 μm to 185.39 ± 28.32 μm (p < 0.05), this smart platform, driven by a 3 mT weak static magnetic field (SMF), successfully mitigated the dependence of the threedimensional colonization of stem cells on pore size, thereby partially overcoming the constraints imposed by conventional geometric topography on deep cell infiltration.

    Article Title: Mechanistic insights into ultraviolet-crosslinked sulfonated hyaluronic acid microspheres for stable biointerfaces on biodegradable cerebrovascular magnesium implants
    Article Snippet: .. Optical microscopy analysis: All samles were examined using an inverted fluorescence Optical icroscope (Nikon Ti-S, Tokyo, Japan), assessing cellular adesion patterns and morphological alteration. .. Surface topogaphy and cellular adhesion patterns were characterized by a eld-emission scanning electron microscope (FE-SEM, ZEISS IGMA 300, Germany) at an accelerating voltage of 5 kV by econdary electron detection [ 26 ].

    Article Title: M2 Macrophage-Derived Small Extracellular Vesicle miR-106a-Loaded QCG Hydrogel Targets the RNF128-LXR Pathway to Reprogram Chondrocyte Cholesterol Metabolism for Osteoarthritis Therapy.
    Article Snippet: Nuclei were counterstained with Hoechst 33342 (C1022, Beyotime, China). .. Images were acquired with an inverted fluorescence microscope (Nikon, Japan), and EdU-positive cells were quantified using ImageJ software. .. Cell senescence was evaluated using the β-Galactosidase Staining Kit (C0602, Beyotime, China).

    Confocal:

    Article Title: Fejerin promotes autophagy via the PINK1-Parkin pathway and is protective against Parkinson’s disease pathology
    Article Snippet: The subsequent day, following a PBS wash, the cells were pairedwith suitably tagged secondary antibodies(1:100, BA1127orBA1126, Boster,Wuhan, China) and kept in the dark at 37 °C for 1 h. Finally, the coverslips were secured onto glass slides using an anti-fade mounting medium laced with DAPI (Abcam, Cambridge, UK) to highlight the cell nuclei. .. Finally, immunofluorescence snapshots were taken, and fluorescence intensity was measured with both a Nikon inverted fluorescence microscope and a confocal microscope. ..

    Software:

    Article Title: 3D-printed PLCL scaffolds for breast reconstructive tissue engineering: a pre-clinical study in a rabbit model
    Article Snippet: At day 7 of differentiation, cells were labelled for 20 min at 37 °C with two fluorescent dyes, 1 μg/ml each: Hoechst 33,342 (Invitrogen—H3570; Thermofisher) and BODIPY 493/503 (Invitrogen—D3922; Thermofisher). .. Following two PBS washes, visualization and quantification were carried out by fluorescence microscopy using a Nikon Eclipse Ts2 – FL inverted microscopes (Nikon; Amstelvee, The Netherlands) with a 10 X objective and NIS-Elements software (Nikon) for image acquisition and analysis. ..

    Analysis:

    Article Title: 3D-printed PLCL scaffolds for breast reconstructive tissue engineering: a pre-clinical study in a rabbit model
    Article Snippet: At day 7 of differentiation, cells were labelled for 20 min at 37 °C with two fluorescent dyes, 1 μg/ml each: Hoechst 33,342 (Invitrogen—H3570; Thermofisher) and BODIPY 493/503 (Invitrogen—D3922; Thermofisher). .. Following two PBS washes, visualization and quantification were carried out by fluorescence microscopy using a Nikon Eclipse Ts2 – FL inverted microscopes (Nikon; Amstelvee, The Netherlands) with a 10 X objective and NIS-Elements software (Nikon) for image acquisition and analysis. ..

    Article Title: Mechanistic insights into ultraviolet-crosslinked sulfonated hyaluronic acid microspheres for stable biointerfaces on biodegradable cerebrovascular magnesium implants
    Article Snippet: .. Optical microscopy analysis: All samles were examined using an inverted fluorescence Optical icroscope (Nikon Ti-S, Tokyo, Japan), assessing cellular adesion patterns and morphological alteration. .. Surface topogaphy and cellular adhesion patterns were characterized by a eld-emission scanning electron microscope (FE-SEM, ZEISS IGMA 300, Germany) at an accelerating voltage of 5 kV by econdary electron detection [ 26 ].

    Construct:

    Article Title: A smart magneto-responsive ternary 3D platform for actively steering stereoscopic infiltration and chronological osteogenic differentiation of BMSCs.
    Article Snippet: The limited effective infiltration of cells into the interior of scaffolds remains a critical bottleneck limiting the therapeutic application of bone tissue engineering.. To address this challenge, this study developed a physically self-assembled ternary smart magneto-responsive composite platform (MGO/CS) based on chitosan, graphene oxide, and superparamagnetic iron oxide nanoparticles (SPIONs).. Although the incorporation of SPIONs reduced the mean pore size of the scaffold from 306.64 ± 52.25 μm to 185.39 ± 28.32 μm (p < 0.05), this smart platform, driven by a 3 mT weak static magnetic field (SMF), successfully mitigated the dependence of the threedimensional colonization of stem cells on pore size, thereby partially overcoming the constraints imposed by conventional geometric topography on deep cell infiltration.

    Staining:

    Article Title: A smart magneto-responsive ternary 3D platform for actively steering stereoscopic infiltration and chronological osteogenic differentiation of BMSCs.
    Article Snippet: The limited effective infiltration of cells into the interior of scaffolds remains a critical bottleneck limiting the therapeutic application of bone tissue engineering.. To address this challenge, this study developed a physically self-assembled ternary smart magneto-responsive composite platform (MGO/CS) based on chitosan, graphene oxide, and superparamagnetic iron oxide nanoparticles (SPIONs).. Although the incorporation of SPIONs reduced the mean pore size of the scaffold from 306.64 ± 52.25 μm to 185.39 ± 28.32 μm (p < 0.05), this smart platform, driven by a 3 mT weak static magnetic field (SMF), successfully mitigated the dependence of the threedimensional colonization of stem cells on pore size, thereby partially overcoming the constraints imposed by conventional geometric topography on deep cell infiltration.

    Article Title: Allogeneic Human Bone Marrow‐Derived Mesenchymal Stem Cells Accelerate Diabetic Wound Healing via Inflammation Suppression and Angiogenesis Promotion: A Preclinical Study
    Article Snippet: After 16–18 h of incubation, HUVECs migrated to the bottom surface of the transwell membranes and were fixed with 4% Paraformaldehyde (PFA; ChemCruz Biochemicals, Netherlands) for 1 h at room temperature, followed by cell staining with 1% crystal violet dye. .. The remaining HUVECs in the upper chamber were scraped out by the swabs, and stained cells were captured by Nikon ECLIPSE Ti‐S Inverted Microscopes afterward. .. The average number of migrated cells was calculated in five random fields through the application of 4′,6‐diamidino‐2‐phenylindole (DAPI, Sigma‐Aldrich, St. Louis, MO) staining, Zeiss Axiovert 200 M Fluorescence Microscope, and Image J software.



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    Image Search Results


    (A) Representative epifluorescence images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Journal: PLOS Biology

    Article Title: The neurohormone tyramine stimulates the secretion of an insulin-like peptide from the Caenorhabditis elegans intestine to modulate the systemic stress response

    doi: 10.1371/journal.pbio.3002997

    Figure Lengend Snippet: (A) Representative epifluorescence images (20×) of L4 animals expressing Pins-3::GFP under basal conditions (20 °C on Nematode Growth Media plates seeded with OP50), under oxidative stress (1 mM FeSO 4, 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous tyramine (15 mM). Scale bar 50 µm. (B) Corresponding quantification of fluorescence levels per worm. Scatter dot plot with relative expression of Pins-3::GFP normalized to basal conditions of each independent experiment. Line at the median. n = 50−200 animals per condition (distributed across 3–4 independent experiments). One-way ANOVA and Dunn’s post hoc test vs. basal were used. * p < 0.05, **** p < 0.0001. (C) Log 2 fold-changes in ins-3 transcript levels in animals exposed to oxidative stress (1 mM FeSO 4 , 2 h) or heat stress (30 °C, 6 h) and in the presence of exogenous Tyramine (15 mM). Negative and positive values indicate down- and up-regulation of ins-3 , respectively. Fold change was calculated as ΔCt basal conditions/ΔCt test conditions. Results are shown as mean ± s.e.m. n = 4 independent experiments. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Article Snippet: For ins-3 and ins-4 expression levels analysis, animals containing the corresponding transcriptional GFP reporter ( Pins-3::GFP and Pins-4:GFP , respectively) were imaged using an epifluorescence microscope (Nikon Eclipse TE2000-5) coupled to a CCD camera (Nikon DS-Qi2) with 20× objective.

    Techniques: Expressing, Fluorescence

    Representative epifluorescence images (40×) of young not gravid adults expressing Pges-1::INS-3::VENUS in wild-type and tyra-3 null mutant background, in the absence or presence of exogenous tyramine (15 mM). Scale bar 25 µm. Fluorescence is observed in the two posterior coelomocytes of worms (inset). Right. Corresponding quantification of fluorescence intensity on the coelomocytes (normalized to wild-type animals without tyramine exposure). Line at the median. n = 35–40 animals per condition distributed across three independent experiments. For conditions with tyramine, a two-tailed Student’s t test vs. the same strain without tyramine was used. * p < 0.05. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Journal: PLOS Biology

    Article Title: The neurohormone tyramine stimulates the secretion of an insulin-like peptide from the Caenorhabditis elegans intestine to modulate the systemic stress response

    doi: 10.1371/journal.pbio.3002997

    Figure Lengend Snippet: Representative epifluorescence images (40×) of young not gravid adults expressing Pges-1::INS-3::VENUS in wild-type and tyra-3 null mutant background, in the absence or presence of exogenous tyramine (15 mM). Scale bar 25 µm. Fluorescence is observed in the two posterior coelomocytes of worms (inset). Right. Corresponding quantification of fluorescence intensity on the coelomocytes (normalized to wild-type animals without tyramine exposure). Line at the median. n = 35–40 animals per condition distributed across three independent experiments. For conditions with tyramine, a two-tailed Student’s t test vs. the same strain without tyramine was used. * p < 0.05. The data underlying this figure can be found at https://osf.io/wfgvs/ .

    Article Snippet: For ins-3 and ins-4 expression levels analysis, animals containing the corresponding transcriptional GFP reporter ( Pins-3::GFP and Pins-4:GFP , respectively) were imaged using an epifluorescence microscope (Nikon Eclipse TE2000-5) coupled to a CCD camera (Nikon DS-Qi2) with 20× objective.

    Techniques: Expressing, Mutagenesis, Fluorescence, Two Tailed Test