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transepithelial electrical resistance teer  (World Precision Instruments)


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    World Precision Instruments transepithelial electrical resistance teer
    Effect of Pseudomonas aeruginosa infection in mono- and dual-cell culture models. (A) IL-8 quantification (pg/mL) after 16 h of infection with (P) aeruginosa. (B) Fold change of <t>Transepithelial</t> <t>Electrical</t> Resistance <t>(TEER)</t> (Ω·cm 2 ) in both models after infection with (P) aeruginosa for 16 h. (C) Bacterial load in colony-forming units (CFU/mL) across the different compartments of the dual-cell air-liquid-interface model, apical, attached (bacteria present within the epithelial cells or firmly attached to the surface), and the basolateral compartment. (D) Orthogonal and cross-sectional views of the mono- and dual-cell culture model after 16 h of infection with (P) aeruginosa (scale bar: 100 µm). Left image, a mono-cell culture infection model showing ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), and cell nuclei (blue, DAPI); right image shows a dual-cell culture model with ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), cell nuclei (blue, DAPI), and macrophages (yellow, CD14). All Images were taken at 40X magnification. Data represent mean ± SD from three biological replicates, each with three technical replicates. Statistical significance was determined by one-way ANOVA with Tukey ’ s multiple comparisons test for IL-8, TEER and CFU comparisons, and is indicated as *p ≤ 0.05, **p ≤ 0.001, *** p ≤ 0.0001, and ****p < 0.0001.
    Transepithelial Electrical Resistance Teer, supplied by World Precision Instruments, used in various techniques. Bioz Stars score: 97/100, based on 3724 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/transepithelial electrical resistance teer/product/World Precision Instruments
    Average 97 stars, based on 3724 article reviews
    transepithelial electrical resistance teer - by Bioz Stars, 2026-05
    97/100 stars

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    1) Product Images from "Host-pathogen-immune interactions in an air-liquid interface airway model"

    Article Title: Host-pathogen-immune interactions in an air-liquid interface airway model

    Journal: Frontiers in Cellular and Infection Microbiology

    doi: 10.3389/fcimb.2026.1788554

    Effect of Pseudomonas aeruginosa infection in mono- and dual-cell culture models. (A) IL-8 quantification (pg/mL) after 16 h of infection with (P) aeruginosa. (B) Fold change of Transepithelial Electrical Resistance (TEER) (Ω·cm 2 ) in both models after infection with (P) aeruginosa for 16 h. (C) Bacterial load in colony-forming units (CFU/mL) across the different compartments of the dual-cell air-liquid-interface model, apical, attached (bacteria present within the epithelial cells or firmly attached to the surface), and the basolateral compartment. (D) Orthogonal and cross-sectional views of the mono- and dual-cell culture model after 16 h of infection with (P) aeruginosa (scale bar: 100 µm). Left image, a mono-cell culture infection model showing ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), and cell nuclei (blue, DAPI); right image shows a dual-cell culture model with ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), cell nuclei (blue, DAPI), and macrophages (yellow, CD14). All Images were taken at 40X magnification. Data represent mean ± SD from three biological replicates, each with three technical replicates. Statistical significance was determined by one-way ANOVA with Tukey ’ s multiple comparisons test for IL-8, TEER and CFU comparisons, and is indicated as *p ≤ 0.05, **p ≤ 0.001, *** p ≤ 0.0001, and ****p < 0.0001.
    Figure Legend Snippet: Effect of Pseudomonas aeruginosa infection in mono- and dual-cell culture models. (A) IL-8 quantification (pg/mL) after 16 h of infection with (P) aeruginosa. (B) Fold change of Transepithelial Electrical Resistance (TEER) (Ω·cm 2 ) in both models after infection with (P) aeruginosa for 16 h. (C) Bacterial load in colony-forming units (CFU/mL) across the different compartments of the dual-cell air-liquid-interface model, apical, attached (bacteria present within the epithelial cells or firmly attached to the surface), and the basolateral compartment. (D) Orthogonal and cross-sectional views of the mono- and dual-cell culture model after 16 h of infection with (P) aeruginosa (scale bar: 100 µm). Left image, a mono-cell culture infection model showing ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), and cell nuclei (blue, DAPI); right image shows a dual-cell culture model with ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), cell nuclei (blue, DAPI), and macrophages (yellow, CD14). All Images were taken at 40X magnification. Data represent mean ± SD from three biological replicates, each with three technical replicates. Statistical significance was determined by one-way ANOVA with Tukey ’ s multiple comparisons test for IL-8, TEER and CFU comparisons, and is indicated as *p ≤ 0.05, **p ≤ 0.001, *** p ≤ 0.0001, and ****p < 0.0001.

    Techniques Used: Infection, Cell Culture, Bacteria



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    transepithelial electrical resistance teer  (World Precision Instruments)
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    World Precision Instruments transepithelial electrical resistance teer
    Effect of Pseudomonas aeruginosa infection in mono- and dual-cell culture models. (A) IL-8 quantification (pg/mL) after 16 h of infection with (P) aeruginosa. (B) Fold change of <t>Transepithelial</t> <t>Electrical</t> Resistance <t>(TEER)</t> (Ω·cm 2 ) in both models after infection with (P) aeruginosa for 16 h. (C) Bacterial load in colony-forming units (CFU/mL) across the different compartments of the dual-cell air-liquid-interface model, apical, attached (bacteria present within the epithelial cells or firmly attached to the surface), and the basolateral compartment. (D) Orthogonal and cross-sectional views of the mono- and dual-cell culture model after 16 h of infection with (P) aeruginosa (scale bar: 100 µm). Left image, a mono-cell culture infection model showing ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), and cell nuclei (blue, DAPI); right image shows a dual-cell culture model with ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), cell nuclei (blue, DAPI), and macrophages (yellow, CD14). All Images were taken at 40X magnification. Data represent mean ± SD from three biological replicates, each with three technical replicates. Statistical significance was determined by one-way ANOVA with Tukey ’ s multiple comparisons test for IL-8, TEER and CFU comparisons, and is indicated as *p ≤ 0.05, **p ≤ 0.001, *** p ≤ 0.0001, and ****p < 0.0001.
    Transepithelial Electrical Resistance Teer, supplied by World Precision Instruments, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/transepithelial electrical resistance teer/product/World Precision Instruments
    Average 97 stars, based on 1 article reviews
    transepithelial electrical resistance teer - by Bioz Stars, 2026-05
    97/100 stars
    		  Buy from Supplier
    transepithelial electric resistance teer values  (World Precision Instruments)
    97
    World Precision Instruments transepithelial electric resistance teer values
    Effect of Pseudomonas aeruginosa infection in mono- and dual-cell culture models. (A) IL-8 quantification (pg/mL) after 16 h of infection with (P) aeruginosa. (B) Fold change of <t>Transepithelial</t> <t>Electrical</t> Resistance <t>(TEER)</t> (Ω·cm 2 ) in both models after infection with (P) aeruginosa for 16 h. (C) Bacterial load in colony-forming units (CFU/mL) across the different compartments of the dual-cell air-liquid-interface model, apical, attached (bacteria present within the epithelial cells or firmly attached to the surface), and the basolateral compartment. (D) Orthogonal and cross-sectional views of the mono- and dual-cell culture model after 16 h of infection with (P) aeruginosa (scale bar: 100 µm). Left image, a mono-cell culture infection model showing ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), and cell nuclei (blue, DAPI); right image shows a dual-cell culture model with ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), cell nuclei (blue, DAPI), and macrophages (yellow, CD14). All Images were taken at 40X magnification. Data represent mean ± SD from three biological replicates, each with three technical replicates. Statistical significance was determined by one-way ANOVA with Tukey ’ s multiple comparisons test for IL-8, TEER and CFU comparisons, and is indicated as *p ≤ 0.05, **p ≤ 0.001, *** p ≤ 0.0001, and ****p < 0.0001.
    Transepithelial Electric Resistance Teer Values, supplied by World Precision Instruments, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/transepithelial electric resistance teer values/product/World Precision Instruments
    Average 97 stars, based on 1 article reviews
    transepithelial electric resistance teer values - by Bioz Stars, 2026-05
    97/100 stars
    		  Buy from Supplier

    Image Search Results


    Effect of Pseudomonas aeruginosa infection in mono- and dual-cell culture models. (A) IL-8 quantification (pg/mL) after 16 h of infection with (P) aeruginosa. (B) Fold change of Transepithelial Electrical Resistance (TEER) (Ω·cm 2 ) in both models after infection with (P) aeruginosa for 16 h. (C) Bacterial load in colony-forming units (CFU/mL) across the different compartments of the dual-cell air-liquid-interface model, apical, attached (bacteria present within the epithelial cells or firmly attached to the surface), and the basolateral compartment. (D) Orthogonal and cross-sectional views of the mono- and dual-cell culture model after 16 h of infection with (P) aeruginosa (scale bar: 100 µm). Left image, a mono-cell culture infection model showing ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), and cell nuclei (blue, DAPI); right image shows a dual-cell culture model with ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), cell nuclei (blue, DAPI), and macrophages (yellow, CD14). All Images were taken at 40X magnification. Data represent mean ± SD from three biological replicates, each with three technical replicates. Statistical significance was determined by one-way ANOVA with Tukey ’ s multiple comparisons test for IL-8, TEER and CFU comparisons, and is indicated as *p ≤ 0.05, **p ≤ 0.001, *** p ≤ 0.0001, and ****p < 0.0001.

    Journal: Frontiers in Cellular and Infection Microbiology

    Article Title: Host-pathogen-immune interactions in an air-liquid interface airway model

    doi: 10.3389/fcimb.2026.1788554

    Figure Lengend Snippet: Effect of Pseudomonas aeruginosa infection in mono- and dual-cell culture models. (A) IL-8 quantification (pg/mL) after 16 h of infection with (P) aeruginosa. (B) Fold change of Transepithelial Electrical Resistance (TEER) (Ω·cm 2 ) in both models after infection with (P) aeruginosa for 16 h. (C) Bacterial load in colony-forming units (CFU/mL) across the different compartments of the dual-cell air-liquid-interface model, apical, attached (bacteria present within the epithelial cells or firmly attached to the surface), and the basolateral compartment. (D) Orthogonal and cross-sectional views of the mono- and dual-cell culture model after 16 h of infection with (P) aeruginosa (scale bar: 100 µm). Left image, a mono-cell culture infection model showing ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), and cell nuclei (blue, DAPI); right image shows a dual-cell culture model with ciliated cells (red, acetylated alpha-tubulin), (P) aeruginosa (green, sfGFP), cell nuclei (blue, DAPI), and macrophages (yellow, CD14). All Images were taken at 40X magnification. Data represent mean ± SD from three biological replicates, each with three technical replicates. Statistical significance was determined by one-way ANOVA with Tukey ’ s multiple comparisons test for IL-8, TEER and CFU comparisons, and is indicated as *p ≤ 0.05, **p ≤ 0.001, *** p ≤ 0.0001, and ****p < 0.0001.

    Article Snippet: In addition, Transepithelial electrical resistance (TEER) was measured using a voltohmmeter (e.g., EVOM2, World Precision Instruments) with STX electrodes according to the manufacturer’s instructions.

    Techniques: Infection, Cell Culture, Bacteria