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fluorescence inverted microscope  (Nikon)


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    Structured Review

    Nikon fluorescence inverted microscope
    Fluorescence Inverted Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 14758 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+ni-e+fluorescent+microscope/Inverted+Microscopes/pm40077620-55-35-38
    Average 99 stars, based on 14758 article reviews
    fluorescence inverted microscope - by Bioz Stars, 2026-10
    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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    a Phase contrast and H&E staining of NC- and BA-MBOs. Three experiments were repeated with similar results. b Immunostaining of CK19 (green), CD31 (white), VIM (red) and Nucleus (blue; DAPI) in MBOs. Abundance of CK19 + cells ( n = 12 fields for NC or 14 fields for BA examined over 3 independent samples) and average size of gland-like structures ( n = 11 fields for NC or 7 fields for BA examined over 3 independent samples) were quantified (Mean ± SD). c Immunostaining of ZO1 (green), β-catenin (red), CK19 (white) and nucleus (blue; DAPI) in MBOs. Graphs show CK19 + cells exhibiting apical-basal polarity (Mean ± SD; n = 12 fields per 3 organoids). d Alcian Blue staining for MBOs. Mucin production in epithelium was determined by ratio of Alcian Blue + areas in CK19 + (from separately examined <t>immunofluorescence</t> data) areas (Mean ± SD; n = 15 fields [for NC] or 12 fields [for BA] examined over 3 independent samples). e Heatmap (left) and Volcano plot (right) of differentially expressed genes between NC- and BA-MBOs (up in BA: 350; down in BA: 851). f DAB staining of MBOs for MMP-7 and OPN. The staining intensities were quantified by imaging analysis (Mean ± SD; n = 12 fields per 3 organoids). g Representative plots and quantification of FACS for hybrid cells (pan-CK + /VIM + ) and cholangiocytes (pan-CK + /VIM − ) in Mono and MBO. The number and cell ratio were quantified (Mean ± SD; n = 6). For b – d , f , g , the p -values were shown in plots and were determined using two-tailed Welch’s t -test.
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    Image Search Results


    a Phase contrast and H&E staining of NC- and BA-MBOs. Three experiments were repeated with similar results. b Immunostaining of CK19 (green), CD31 (white), VIM (red) and Nucleus (blue; DAPI) in MBOs. Abundance of CK19 + cells ( n = 12 fields for NC or 14 fields for BA examined over 3 independent samples) and average size of gland-like structures ( n = 11 fields for NC or 7 fields for BA examined over 3 independent samples) were quantified (Mean ± SD). c Immunostaining of ZO1 (green), β-catenin (red), CK19 (white) and nucleus (blue; DAPI) in MBOs. Graphs show CK19 + cells exhibiting apical-basal polarity (Mean ± SD; n = 12 fields per 3 organoids). d Alcian Blue staining for MBOs. Mucin production in epithelium was determined by ratio of Alcian Blue + areas in CK19 + (from separately examined immunofluorescence data) areas (Mean ± SD; n = 15 fields [for NC] or 12 fields [for BA] examined over 3 independent samples). e Heatmap (left) and Volcano plot (right) of differentially expressed genes between NC- and BA-MBOs (up in BA: 350; down in BA: 851). f DAB staining of MBOs for MMP-7 and OPN. The staining intensities were quantified by imaging analysis (Mean ± SD; n = 12 fields per 3 organoids). g Representative plots and quantification of FACS for hybrid cells (pan-CK + /VIM + ) and cholangiocytes (pan-CK + /VIM − ) in Mono and MBO. The number and cell ratio were quantified (Mean ± SD; n = 6). For b – d , f , g , the p -values were shown in plots and were determined using two-tailed Welch’s t -test.

    Journal: Nature Communications

    Article Title: Cellular crosstalk mediated by TGF-β drives epithelial-mesenchymal transition in patient-derived multi-compartment biliary organoids

    doi: 10.1038/s41467-025-61442-5

    Figure Lengend Snippet: a Phase contrast and H&E staining of NC- and BA-MBOs. Three experiments were repeated with similar results. b Immunostaining of CK19 (green), CD31 (white), VIM (red) and Nucleus (blue; DAPI) in MBOs. Abundance of CK19 + cells ( n = 12 fields for NC or 14 fields for BA examined over 3 independent samples) and average size of gland-like structures ( n = 11 fields for NC or 7 fields for BA examined over 3 independent samples) were quantified (Mean ± SD). c Immunostaining of ZO1 (green), β-catenin (red), CK19 (white) and nucleus (blue; DAPI) in MBOs. Graphs show CK19 + cells exhibiting apical-basal polarity (Mean ± SD; n = 12 fields per 3 organoids). d Alcian Blue staining for MBOs. Mucin production in epithelium was determined by ratio of Alcian Blue + areas in CK19 + (from separately examined immunofluorescence data) areas (Mean ± SD; n = 15 fields [for NC] or 12 fields [for BA] examined over 3 independent samples). e Heatmap (left) and Volcano plot (right) of differentially expressed genes between NC- and BA-MBOs (up in BA: 350; down in BA: 851). f DAB staining of MBOs for MMP-7 and OPN. The staining intensities were quantified by imaging analysis (Mean ± SD; n = 12 fields per 3 organoids). g Representative plots and quantification of FACS for hybrid cells (pan-CK + /VIM + ) and cholangiocytes (pan-CK + /VIM − ) in Mono and MBO. The number and cell ratio were quantified (Mean ± SD; n = 6). For b – d , f , g , the p -values were shown in plots and were determined using two-tailed Welch’s t -test.

    Article Snippet: Bright field images were captured using a light microscope (Olympus, BX43) and immunofluorescence images were captured using either fluorescence (Olympus, BX51; Nikon, ECLIPSE Ni-E) or confocal (Nikon, ECLIPSE Ti; Zeiss, LSM880) microscopes.

    Techniques: Staining, Immunostaining, Immunofluorescence, Imaging, Two Tailed Test

    a Overview of in vitro A8301-mediated TGF-β signal inhibition in BA-MBOs. Created in BioRender. Ayabe, H. (2025) https://BioRender.com/q1pk62z . b Representative plots and quantification of FACS of day 14 MBOs treated with A8301. Number of hybrid (pan-CK + /VIM + ), cholangiocyte (pan-CK + /VIM - ) and mesenchymal (pan-CK − /VIM + ) cells were quantified (Mean ± SD; n = 12 organoids). c Images of MBOs treated with A8301 captured before collection and after whole-mount immunostaining (CK19: red, CD31: green, VIM: white). Abundance of CK19 + structures (Mean ± SD; n = 9 organoids examined over 3 independent experiments) and size distribution of PBG-like structures were quantified ( n = 39-104 clusters examined over 3 independent experiments). d Immunostaining of ECAD (green), CK19 (red) and Nucleus (blue; DAPI) in MBOs treated with A8301. ECAD + cells in CK19 + cells in the field were quantified (Mean ± SD; n = 12 fields from 3 organoids). e Immunostaining of ZO1 (green), CK19 (red) and Nucleus (blue; DAPI) in MBO treated with A8301. ZO1 + cells in CK19 + cells per field were quantified (Mean ± SD; n = 12 fields from 3 organoids). f Alcian blue staining of MBOs treated with A8301. Mucin production was determined by ratio of Alcian Blue + areas in CK19 + (from separately examined immunofluorescence data) areas (Mean ± SD; n = 12 fields from 3 organoids). g Top enriched terms of MSigDB Hallmark 2020 , and GO , sets in serum proteins (reanalyzed from Lertudomphonwanit et al. ) upregulated in BA subjects ( n = 175 patients) vs age-matched normal controls ( n = 9). MF: Molecular Function, BP: Biological Process. h Heatmap of enriched proteins in the EMT pathway in MSigDB Hallmark 2020 sets. ( n = 9 NC and 175 BA subjects). i Serum TGF-β/Activin ligand levels represented by the relative fluorescent unit (RFU; Mean ± SD). ( n = 9 NC and 175 BA subjects). The p -values were shown in plots and were determined using one-way ANOVA with Tukey’s test ( b – f ) and two-tailed Welch’s t -test ( i ).

    Journal: Nature Communications

    Article Title: Cellular crosstalk mediated by TGF-β drives epithelial-mesenchymal transition in patient-derived multi-compartment biliary organoids

    doi: 10.1038/s41467-025-61442-5

    Figure Lengend Snippet: a Overview of in vitro A8301-mediated TGF-β signal inhibition in BA-MBOs. Created in BioRender. Ayabe, H. (2025) https://BioRender.com/q1pk62z . b Representative plots and quantification of FACS of day 14 MBOs treated with A8301. Number of hybrid (pan-CK + /VIM + ), cholangiocyte (pan-CK + /VIM - ) and mesenchymal (pan-CK − /VIM + ) cells were quantified (Mean ± SD; n = 12 organoids). c Images of MBOs treated with A8301 captured before collection and after whole-mount immunostaining (CK19: red, CD31: green, VIM: white). Abundance of CK19 + structures (Mean ± SD; n = 9 organoids examined over 3 independent experiments) and size distribution of PBG-like structures were quantified ( n = 39-104 clusters examined over 3 independent experiments). d Immunostaining of ECAD (green), CK19 (red) and Nucleus (blue; DAPI) in MBOs treated with A8301. ECAD + cells in CK19 + cells in the field were quantified (Mean ± SD; n = 12 fields from 3 organoids). e Immunostaining of ZO1 (green), CK19 (red) and Nucleus (blue; DAPI) in MBO treated with A8301. ZO1 + cells in CK19 + cells per field were quantified (Mean ± SD; n = 12 fields from 3 organoids). f Alcian blue staining of MBOs treated with A8301. Mucin production was determined by ratio of Alcian Blue + areas in CK19 + (from separately examined immunofluorescence data) areas (Mean ± SD; n = 12 fields from 3 organoids). g Top enriched terms of MSigDB Hallmark 2020 , and GO , sets in serum proteins (reanalyzed from Lertudomphonwanit et al. ) upregulated in BA subjects ( n = 175 patients) vs age-matched normal controls ( n = 9). MF: Molecular Function, BP: Biological Process. h Heatmap of enriched proteins in the EMT pathway in MSigDB Hallmark 2020 sets. ( n = 9 NC and 175 BA subjects). i Serum TGF-β/Activin ligand levels represented by the relative fluorescent unit (RFU; Mean ± SD). ( n = 9 NC and 175 BA subjects). The p -values were shown in plots and were determined using one-way ANOVA with Tukey’s test ( b – f ) and two-tailed Welch’s t -test ( i ).

    Article Snippet: Bright field images were captured using a light microscope (Olympus, BX43) and immunofluorescence images were captured using either fluorescence (Olympus, BX51; Nikon, ECLIPSE Ni-E) or confocal (Nikon, ECLIPSE Ti; Zeiss, LSM880) microscopes.

    Techniques: In Vitro, Inhibition, Immunostaining, Staining, Immunofluorescence, Two Tailed Test