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envision plate reader  (Revvity)


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    Structured Review

    Revvity envision plate reader
    Envision Plate Reader, supplied by Revvity, used in various techniques. Bioz Stars score: 96/100, based on 14032 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/envision+xcite+multimode+plate+reader/EnVision+XCite+multimode+plate+reader/pm42778593-590-26-29
    Average 96 stars, based on 14032 article reviews
    envision plate reader - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    CCK-8 Assay:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Control:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Incubation:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Infection:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Oligomer Restriction:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Spectrophotometry:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Lysis:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Fluorescence:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Concentration Assay:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    High Performance Liquid Chromatography:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Purification:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Synthesized:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Luciferase:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Centrifugation:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Irradiation:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole

    Staining:

    Article Title: MMEJ repair of breaks at TA repeats maintains ecDNA and cancer fitness.
    Article Snippet: 1 h incubation at room temperature. 30 μl of Detection reagent was then added per well, the plates were incubated for 45 min at room temperature, and luminescence was read on an Envision plate reader (Revvity). The forked DNA substrate was prepared as follows: oligos 1–3 were mixed (1:1:1) in a buffer containing 10 mM Tris-HCl, pH 7.5, 50 mM NaCl, and 1 mM EDTA, heated to 95 °C for 5 min, and coole



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