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brdu cell proliferation enzyme  (Danaher Inc)


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    Danaher Inc brdu cell proliferation enzyme
    Brdu Cell Proliferation Enzyme, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 190 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/brdu+cell+proliferation+enzyme/BrdU+Cell+Proliferation+Assay+Kit+200+test/pmc10031244-49-12-20
    Average 99 stars, based on 190 article reviews
    brdu cell proliferation enzyme - by Bioz Stars, 2026-09
    99/100 stars

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    Enzyme-linked Immunosorbent Assay:

    Article Title: PTEN‐AKT pathway attenuates apoptosis and adverse remodeling in ponatinib‐induced skeletal muscle toxicity following BMP‐7 treatment
    Article Snippet: .. The effect of ponatinib and BMP‐7 on cell proliferation was determined by BrdU Cell Proliferation enzyme‐linked immunosorbent assay (ELISA) Kit (Abcam; cat# ab126556). .. Sol8 cells were plated in a 96‐well plate (10 4 cells/well) and treated with 8 μM ponatinib and 500 ng/mL of BMP‐7 (Bioclone; cat# PA‐0401) for 24 h, which was then replaced with fresh DMEM for 24 h. Manufacturer's protocol provided with the kit was used to perform the cell proliferation assay.



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    Cell clonogenic growth <t>and</t> <t>proliferation.</t> ( A ) Number of A498, KTCTL26, and 786O cell clones exposed to 1 µM sunitinib (ST), 5 µM sulforaphane (SFN), or both (DT). Cells were subjected to the assay shortly after drug exposure (short-term incubation) or after re-exposure following an 8 week pre-incubation (long-term incubation). Controls (C) are without drugs. Error bars indicate standard deviation, n = 3. * indicates significant difference to untreated controls. ( B ) Evaluation by <t>BrdU</t> incorporation. A498, Caki1, KTCTL26, and 786O cells were subjected to the assay immediately after drug application (short-term incubation) or following an 8 week pre-incubation (long-term incubation). Controls (C) are without drugs. Error bars indicate standard deviation. * Indicates significant down-regulation, # indicates significant up-regulation to untreated controls set to 100% (indicated by a black line). n = 3.
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    Cell clonogenic growth and proliferation. ( A ) Number of A498, KTCTL26, and 786O cell clones exposed to 1 µM sunitinib (ST), 5 µM sulforaphane (SFN), or both (DT). Cells were subjected to the assay shortly after drug exposure (short-term incubation) or after re-exposure following an 8 week pre-incubation (long-term incubation). Controls (C) are without drugs. Error bars indicate standard deviation, n = 3. * indicates significant difference to untreated controls. ( B ) Evaluation by BrdU incorporation. A498, Caki1, KTCTL26, and 786O cells were subjected to the assay immediately after drug application (short-term incubation) or following an 8 week pre-incubation (long-term incubation). Controls (C) are without drugs. Error bars indicate standard deviation. * Indicates significant down-regulation, # indicates significant up-regulation to untreated controls set to 100% (indicated by a black line). n = 3.

    Journal: Cancers

    Article Title: Concomitant Use of Sulforaphane Enhances Antitumor Efficacy of Sunitinib in Renal Cell Carcinoma In Vitro

    doi: 10.3390/cancers14194643

    Figure Lengend Snippet: Cell clonogenic growth and proliferation. ( A ) Number of A498, KTCTL26, and 786O cell clones exposed to 1 µM sunitinib (ST), 5 µM sulforaphane (SFN), or both (DT). Cells were subjected to the assay shortly after drug exposure (short-term incubation) or after re-exposure following an 8 week pre-incubation (long-term incubation). Controls (C) are without drugs. Error bars indicate standard deviation, n = 3. * indicates significant difference to untreated controls. ( B ) Evaluation by BrdU incorporation. A498, Caki1, KTCTL26, and 786O cells were subjected to the assay immediately after drug application (short-term incubation) or following an 8 week pre-incubation (long-term incubation). Controls (C) are without drugs. Error bars indicate standard deviation. * Indicates significant down-regulation, # indicates significant up-regulation to untreated controls set to 100% (indicated by a black line). n = 3.

    Article Snippet: Cell proliferation was measured using a BrdU (5-bromo-2′-deoxyuridine) cell proliferation enzyme-linked immunosorbent assay (ELISA) kit (Calbiochem/Merck Biosciences, Darmstadt, Germany).

    Techniques: Clone Assay, Incubation, Standard Deviation, BrdU Incorporation Assay