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Servicebio Inc lung tissue sections
Lung Tissue Sections, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lung tissue sections/product/Servicebio Inc
Average 86 stars, based on 1 article reviews
lung tissue sections - by Bioz Stars, 2026-05
86/100 stars

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Proteintech lung tissue sections
Dfa-miR-276-3p as a prime exacerbates DFE-induced airway inflammation in vivo . ( A ) Schematic diagram for construction of AAV-dfa-miR-276-3p-overexpressing mouse models. ( B ) Immunofluorescence assay detects co-expression of EGFP (green) and Claudin-1 (red) in mouse <t>lung</t> <t>tissues,</t> and the nuclei are stained with DAPI (blue) ( n = 3). Scale bar = 50 μm. ( C ) qPCR assay quantifies EGFP mRNA expression in mouse lung tissues. ( D ) qPCR assay quantifies dfa-miR-276-3p expression in mouse lung tissues. ( E ) Schematic diagram for construction of a mouse model of airway sensitization following AAV-dfa-miR-276-3p overexpression in lungs. ( F ) Total cell counts in mouse BALF ( n = 3). ( G ) ELISA measures IL-4 levels in mouse BALF ( n = 3). ( H ) ELISA measures IL-5 levels in mouse BALF ( n = 3). ( I ) ELISA measures IgE <t>antibody</t> levels in mouse serum samples ( n = 6). ( J ) ELISA measures IL-10 levels in mouse BALF ( n = 3). ( K ) HE and PAS staining of representative lung <t>sections</t> ( n = 3). Scale bar = 100 μm. ns, not significant, * P < 0.05, ** P < 0.01, and *** P < 0.001. Data are presented as means ± SEM. Difference of means among groups is tested for statistical significance with ANOVA, followed by Tukey’s post hoc test.
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Servicebio Inc lung tissue sections
Dfa-miR-276-3p as a prime exacerbates DFE-induced airway inflammation in vivo . ( A ) Schematic diagram for construction of AAV-dfa-miR-276-3p-overexpressing mouse models. ( B ) Immunofluorescence assay detects co-expression of EGFP (green) and Claudin-1 (red) in mouse <t>lung</t> <t>tissues,</t> and the nuclei are stained with DAPI (blue) ( n = 3). Scale bar = 50 μm. ( C ) qPCR assay quantifies EGFP mRNA expression in mouse lung tissues. ( D ) qPCR assay quantifies dfa-miR-276-3p expression in mouse lung tissues. ( E ) Schematic diagram for construction of a mouse model of airway sensitization following AAV-dfa-miR-276-3p overexpression in lungs. ( F ) Total cell counts in mouse BALF ( n = 3). ( G ) ELISA measures IL-4 levels in mouse BALF ( n = 3). ( H ) ELISA measures IL-5 levels in mouse BALF ( n = 3). ( I ) ELISA measures IgE <t>antibody</t> levels in mouse serum samples ( n = 6). ( J ) ELISA measures IL-10 levels in mouse BALF ( n = 3). ( K ) HE and PAS staining of representative lung <t>sections</t> ( n = 3). Scale bar = 100 μm. ns, not significant, * P < 0.05, ** P < 0.01, and *** P < 0.001. Data are presented as means ± SEM. Difference of means among groups is tested for statistical significance with ANOVA, followed by Tukey’s post hoc test.
Lung Tissue Sections, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lung tissue sections/product/Servicebio Inc
Average 86 stars, based on 1 article reviews
lung tissue sections - by Bioz Stars, 2026-05
86/100 stars
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99
Beyotime lung tissue sections
Dfa-miR-276-3p as a prime exacerbates DFE-induced airway inflammation in vivo . ( A ) Schematic diagram for construction of AAV-dfa-miR-276-3p-overexpressing mouse models. ( B ) Immunofluorescence assay detects co-expression of EGFP (green) and Claudin-1 (red) in mouse <t>lung</t> <t>tissues,</t> and the nuclei are stained with DAPI (blue) ( n = 3). Scale bar = 50 μm. ( C ) qPCR assay quantifies EGFP mRNA expression in mouse lung tissues. ( D ) qPCR assay quantifies dfa-miR-276-3p expression in mouse lung tissues. ( E ) Schematic diagram for construction of a mouse model of airway sensitization following AAV-dfa-miR-276-3p overexpression in lungs. ( F ) Total cell counts in mouse BALF ( n = 3). ( G ) ELISA measures IL-4 levels in mouse BALF ( n = 3). ( H ) ELISA measures IL-5 levels in mouse BALF ( n = 3). ( I ) ELISA measures IgE <t>antibody</t> levels in mouse serum samples ( n = 6). ( J ) ELISA measures IL-10 levels in mouse BALF ( n = 3). ( K ) HE and PAS staining of representative lung <t>sections</t> ( n = 3). Scale bar = 100 μm. ns, not significant, * P < 0.05, ** P < 0.01, and *** P < 0.001. Data are presented as means ± SEM. Difference of means among groups is tested for statistical significance with ANOVA, followed by Tukey’s post hoc test.
Lung Tissue Sections, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lung tissue sections/product/Beyotime
Average 99 stars, based on 1 article reviews
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Dfa-miR-276-3p as a prime exacerbates DFE-induced airway inflammation in vivo . ( A ) Schematic diagram for construction of AAV-dfa-miR-276-3p-overexpressing mouse models. ( B ) Immunofluorescence assay detects co-expression of EGFP (green) and Claudin-1 (red) in mouse lung tissues, and the nuclei are stained with DAPI (blue) ( n = 3). Scale bar = 50 μm. ( C ) qPCR assay quantifies EGFP mRNA expression in mouse lung tissues. ( D ) qPCR assay quantifies dfa-miR-276-3p expression in mouse lung tissues. ( E ) Schematic diagram for construction of a mouse model of airway sensitization following AAV-dfa-miR-276-3p overexpression in lungs. ( F ) Total cell counts in mouse BALF ( n = 3). ( G ) ELISA measures IL-4 levels in mouse BALF ( n = 3). ( H ) ELISA measures IL-5 levels in mouse BALF ( n = 3). ( I ) ELISA measures IgE antibody levels in mouse serum samples ( n = 6). ( J ) ELISA measures IL-10 levels in mouse BALF ( n = 3). ( K ) HE and PAS staining of representative lung sections ( n = 3). Scale bar = 100 μm. ns, not significant, * P < 0.05, ** P < 0.01, and *** P < 0.001. Data are presented as means ± SEM. Difference of means among groups is tested for statistical significance with ANOVA, followed by Tukey’s post hoc test.

Journal: Microbiology Spectrum

Article Title: A novel role of Dermatophagoides farinae -derived miR-276-3p in aggravating mite-induced allergic airway inflammation

doi: 10.1128/spectrum.01923-25

Figure Lengend Snippet: Dfa-miR-276-3p as a prime exacerbates DFE-induced airway inflammation in vivo . ( A ) Schematic diagram for construction of AAV-dfa-miR-276-3p-overexpressing mouse models. ( B ) Immunofluorescence assay detects co-expression of EGFP (green) and Claudin-1 (red) in mouse lung tissues, and the nuclei are stained with DAPI (blue) ( n = 3). Scale bar = 50 μm. ( C ) qPCR assay quantifies EGFP mRNA expression in mouse lung tissues. ( D ) qPCR assay quantifies dfa-miR-276-3p expression in mouse lung tissues. ( E ) Schematic diagram for construction of a mouse model of airway sensitization following AAV-dfa-miR-276-3p overexpression in lungs. ( F ) Total cell counts in mouse BALF ( n = 3). ( G ) ELISA measures IL-4 levels in mouse BALF ( n = 3). ( H ) ELISA measures IL-5 levels in mouse BALF ( n = 3). ( I ) ELISA measures IgE antibody levels in mouse serum samples ( n = 6). ( J ) ELISA measures IL-10 levels in mouse BALF ( n = 3). ( K ) HE and PAS staining of representative lung sections ( n = 3). Scale bar = 100 μm. ns, not significant, * P < 0.05, ** P < 0.01, and *** P < 0.001. Data are presented as means ± SEM. Difference of means among groups is tested for statistical significance with ANOVA, followed by Tukey’s post hoc test.

Article Snippet: Sections or cell culture slides were blocked with 10% goat serum at room temperature, and the cell culture slides were incubated with the primary anti-NF-κB p65 antibody (Cell Signaling Technology, Inc.), while the lung tissue sections were incubated with the primary anti-claudin 1 antibody (Proteintech, Manchester, UK).

Techniques: In Vivo, Immunofluorescence, Expressing, Staining, Over Expression, Enzyme-linked Immunosorbent Assay

Dfa-miR-276-3p promotes DFE-induced airway inflammation through inhibiting STC1 expression to regulate ROS/NF-κB pathway in vivo . ( A ) Schematic diagram for different treatments of mice. ( B ) Total cell counts in mouse BALF ( n = 3). ( C ) ELISA measures IL-4 levels in mouse BALF ( n = 3). ( D ) ELISA measures IL-5 levels in mouse BALF ( n = 3). ( E ) ELISA measures IgE antibody levels in mouse serum samples ( n = 6). ( F ) ELISA measures IL-10 levels in mouse BALF ( n = 3). ( G ) HE and PAS staining of representative lung sections ( n = 3). Scale bar = 100 μm. ( H ) ROS levels in mouse lung tissues ( n = 6). ( I and J ) Western blotting determines STC1, NF-κB p65, and p-p65 protein expression in mouse lung tissues ( n = 3). ns, not significant, * P < 0.05, ** P < 0.01, and *** P < 0.001. Data are presented as means ± SEM. Difference of means among groups was tested for statistical significance with ANOVA, followed by Tukey’s post hoc test.

Journal: Microbiology Spectrum

Article Title: A novel role of Dermatophagoides farinae -derived miR-276-3p in aggravating mite-induced allergic airway inflammation

doi: 10.1128/spectrum.01923-25

Figure Lengend Snippet: Dfa-miR-276-3p promotes DFE-induced airway inflammation through inhibiting STC1 expression to regulate ROS/NF-κB pathway in vivo . ( A ) Schematic diagram for different treatments of mice. ( B ) Total cell counts in mouse BALF ( n = 3). ( C ) ELISA measures IL-4 levels in mouse BALF ( n = 3). ( D ) ELISA measures IL-5 levels in mouse BALF ( n = 3). ( E ) ELISA measures IgE antibody levels in mouse serum samples ( n = 6). ( F ) ELISA measures IL-10 levels in mouse BALF ( n = 3). ( G ) HE and PAS staining of representative lung sections ( n = 3). Scale bar = 100 μm. ( H ) ROS levels in mouse lung tissues ( n = 6). ( I and J ) Western blotting determines STC1, NF-κB p65, and p-p65 protein expression in mouse lung tissues ( n = 3). ns, not significant, * P < 0.05, ** P < 0.01, and *** P < 0.001. Data are presented as means ± SEM. Difference of means among groups was tested for statistical significance with ANOVA, followed by Tukey’s post hoc test.

Article Snippet: Sections or cell culture slides were blocked with 10% goat serum at room temperature, and the cell culture slides were incubated with the primary anti-NF-κB p65 antibody (Cell Signaling Technology, Inc.), while the lung tissue sections were incubated with the primary anti-claudin 1 antibody (Proteintech, Manchester, UK).

Techniques: Expressing, In Vivo, Enzyme-linked Immunosorbent Assay, Staining, Western Blot