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iressa  (Bio-Techne corporation)


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    Structured Review

    Bio-Techne corporation iressa
    Iressa, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 369 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/biacore+3000+optical+biosensor/Iressa/custom%403000%4041663757
    Average 94 stars, based on 369 article reviews
    iressa - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Incubation:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Transfection:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Cell Culture:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Electroporation:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Milk:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Staining:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Positive Control:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Immunostaining:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Control:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo

    Inhibition:

    Article Title: An integrin beta-1-anchored bicaudal C1-polycystin-1 module essential for tubular morphogenesis in polycystic kidney disease
    Article Snippet: nson, UK), plated into 96 well plates in triplicate and incubated for 30 min at 37°C to facilitate gel formation. Cells were then cultured for 12days in the presence of vehicle (DMSO) or 50 μM CK-666 (Tocris, UK). Media was replaced every 2 days. The percentage of tubular structures was calculated from 3 independent wells per treatment. Cells were transfected using Lipofectamine 3000 (Life Technolo



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