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airway epithelial cells  (Cell Applications Inc)


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    Structured Review

    Cell Applications Inc airway epithelial cells
    Bovine primary respiratory and immortalized mammary gland cells infected with different swine and avian IAVs. (A) Bovine primary nasal turbinate and tracheal <t>epithelial</t> cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at a multiplicity of infection (MOI) of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of the integrated fluorescence density from three separate biological repeats were compared among bovine cells infected with different IAVs. The result was analyzed by using a one-way ANOVA followed by Tukey’s multiple comparison. (C) Four bovine cells were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at an MOI of 0.1. The supernatants were collected at 12 and 36 h post-infection and were titrated on MDCK cells. The result was analyzed by using a two-way ANOVA (* P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001).
    Airway Epithelial Cells, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gi+epithelial+cell+coating+solution/GI+Epithelial+Cell+Coating+Solution/pmc12239592-166-0-19
    Average 94 stars, based on 1 article reviews
    airway epithelial cells - by Bioz Stars, 2026-09
    94/100 stars

    Images

    1) Product Images from "Outcomes of experimental infection of calves with swine influenza H3N2 virus"

    Article Title: Outcomes of experimental infection of calves with swine influenza H3N2 virus

    Journal: mBio

    doi: 10.1128/mbio.03957-24

    Bovine primary respiratory and immortalized mammary gland cells infected with different swine and avian IAVs. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at a multiplicity of infection (MOI) of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of the integrated fluorescence density from three separate biological repeats were compared among bovine cells infected with different IAVs. The result was analyzed by using a one-way ANOVA followed by Tukey’s multiple comparison. (C) Four bovine cells were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at an MOI of 0.1. The supernatants were collected at 12 and 36 h post-infection and were titrated on MDCK cells. The result was analyzed by using a two-way ANOVA (* P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001).
    Figure Legend Snippet: Bovine primary respiratory and immortalized mammary gland cells infected with different swine and avian IAVs. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at a multiplicity of infection (MOI) of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of the integrated fluorescence density from three separate biological repeats were compared among bovine cells infected with different IAVs. The result was analyzed by using a one-way ANOVA followed by Tukey’s multiple comparison. (C) Four bovine cells were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at an MOI of 0.1. The supernatants were collected at 12 and 36 h post-infection and were titrated on MDCK cells. The result was analyzed by using a two-way ANOVA (* P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001).

    Techniques Used: Infection, Staining, Fluorescence, Comparison

    Bovine primary respiratory and immortalized mammary gland cells infected with PR8 and rgH5N1/PR8. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with the PR8 or rgH5N1/PR8 at a multiplicity of infection of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of integrated fluorescence density from three separate biological repeats were compared in each bovine cell line infected with PR8 or rgH5N1/PR8. The result was analyzed by using a Student’s t test (** P < 0.01, *** P < 0.001, and **** P < 0.0001).
    Figure Legend Snippet: Bovine primary respiratory and immortalized mammary gland cells infected with PR8 and rgH5N1/PR8. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with the PR8 or rgH5N1/PR8 at a multiplicity of infection of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of integrated fluorescence density from three separate biological repeats were compared in each bovine cell line infected with PR8 or rgH5N1/PR8. The result was analyzed by using a Student’s t test (** P < 0.01, *** P < 0.001, and **** P < 0.0001).

    Techniques Used: Infection, Staining, Fluorescence

    Related Articles

    other:

    Article Title: Compositions and methods for organ-protective expression and modulation of coding ribonucleic acids
    Article Snippet: 96-well microplate wells were pretreated with GI Epithelial Cell Coating Solution (Cell Applications, Inc., reference 025-05) and 60,000 cells per well were seeded.

    Article Title: Compositions and methods for organ-protective expression and modulation of coding ribonucleic acids
    Article Snippet: 96-well microplate wells were pretreated with GI Epithelial Cell Coating Solution (Cell Applications, Inc., reference 025-05) and 60,000 cells per well were seeded.

    Article Title: Compositions and methods for organ-protective expression and modulation of coding ribonucleic acids
    Article Snippet: 96-well microplate wells were pretreated with GI Epithelial Cell Coating Solution (Cell Applications, Inc., reference 025-05) and 60,000 cells per well were seeded.



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    Image Search Results


    Bovine primary respiratory and immortalized mammary gland cells infected with different swine and avian IAVs. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at a multiplicity of infection (MOI) of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of the integrated fluorescence density from three separate biological repeats were compared among bovine cells infected with different IAVs. The result was analyzed by using a one-way ANOVA followed by Tukey’s multiple comparison. (C) Four bovine cells were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at an MOI of 0.1. The supernatants were collected at 12 and 36 h post-infection and were titrated on MDCK cells. The result was analyzed by using a two-way ANOVA (* P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001).

    Journal: mBio

    Article Title: Outcomes of experimental infection of calves with swine influenza H3N2 virus

    doi: 10.1128/mbio.03957-24

    Figure Lengend Snippet: Bovine primary respiratory and immortalized mammary gland cells infected with different swine and avian IAVs. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at a multiplicity of infection (MOI) of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of the integrated fluorescence density from three separate biological repeats were compared among bovine cells infected with different IAVs. The result was analyzed by using a one-way ANOVA followed by Tukey’s multiple comparison. (C) Four bovine cells were infected with swine H3N2, avian rgH5N1/PR8, or avian H9N2 viruses at an MOI of 0.1. The supernatants were collected at 12 and 36 h post-infection and were titrated on MDCK cells. The result was analyzed by using a two-way ANOVA (* P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001).

    Article Snippet: Airway epithelial cells were incubated at 37°C with 5% CO 2 and maintained using bronchia/trachea epithelial cell basal medium (Cell Applications, Inc.) supplemented with 10% FBS (Gibco, Waltham, MA, USA).

    Techniques: Infection, Staining, Fluorescence, Comparison

    Bovine primary respiratory and immortalized mammary gland cells infected with PR8 and rgH5N1/PR8. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with the PR8 or rgH5N1/PR8 at a multiplicity of infection of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of integrated fluorescence density from three separate biological repeats were compared in each bovine cell line infected with PR8 or rgH5N1/PR8. The result was analyzed by using a Student’s t test (** P < 0.01, *** P < 0.001, and **** P < 0.0001).

    Journal: mBio

    Article Title: Outcomes of experimental infection of calves with swine influenza H3N2 virus

    doi: 10.1128/mbio.03957-24

    Figure Lengend Snippet: Bovine primary respiratory and immortalized mammary gland cells infected with PR8 and rgH5N1/PR8. (A) Bovine primary nasal turbinate and tracheal epithelial cells, as well as immortalized mammary gland epithelial cells and fibroblasts, were infected with the PR8 or rgH5N1/PR8 at a multiplicity of infection of 1. At 24 h post-infection, cells were fixed and stained with an anti-IAV NP monoclonal antibody. (B) Mean values of integrated fluorescence density from three separate biological repeats were compared in each bovine cell line infected with PR8 or rgH5N1/PR8. The result was analyzed by using a Student’s t test (** P < 0.01, *** P < 0.001, and **** P < 0.0001).

    Article Snippet: Airway epithelial cells were incubated at 37°C with 5% CO 2 and maintained using bronchia/trachea epithelial cell basal medium (Cell Applications, Inc.) supplemented with 10% FBS (Gibco, Waltham, MA, USA).

    Techniques: Infection, Staining, Fluorescence