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Victor3 model

Manufactured by PerkinElmer
Sourced in United States

The Victor3 is a multi-mode microplate reader designed for a variety of applications, including absorbance, fluorescence, and luminescence measurements. It features high-performance optics and a sensitive detector to provide accurate and reliable results. The Victor3 supports a wide range of microplate formats and can be used in various research and diagnostic settings.

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2 protocols using victor3 model

1

Spectroscopic Analyses of Bioactive Compounds

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Colour measurements were made with a hand-held tristimulus reflectance spectrocolorimeter (Minolta Co., Model CM-508-d, Japan). For total anthocyanin and phenolic compound contents, and antioxidant capacity (TEAC assay), a UV- VIS spectrophotometer (model V-630, JASCO, Japan) was used. For the determination of antioxidant capacity evaluated by ORAC assay, fluorescence measurements were made by means of a Multilabel Microplate Reader (Perkin Elmer, Victor3 model, USA). Fluorescence measurements in Caenorhabditis elegans assays were performed in a Spark 20M Multimode Microplate Reader (Tecan, NC, USA).
AAPH (2,2′-Azobis (2-methylpropionamidine) dihydrochloride, ABTS (2,2 -azinobis (3-ethylbenzothiazoline)-6-sulfonate), fluorescein sodium salt, gallic acid (GA), Trolox (C14H18O4) and 2,7 – dichlorodihydrofluorescein diacetate (H2DCF-DA) were purchased from Sigma-Aldrich (St. Louis, USA). Ethyl alcohol, sodium acetate, sodium carbonate, and Tween 80 were from Biopack (Buenos Aires, Argentina). Folin Ciocalteau reagent, dipotassium hydrogen phosphate, potassium dihydrogen phosphate, disodium hydrogen phosphate, hydrochloric acid, potassium chloride, sodium chloride, sodium hydroxide, manganese sulphate, and malt extract agar (MEA) were purchased from Merck (Darmstadt, Germany).
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2

Cell Viability Assay Using MTT

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Cell viability was measured using the MTT assay. Cells were seeded at two densities of 1 × 104 and 1.5 × 104 cells per well in 96-well plates and maintained in the appropriate culture medium. After 24 h, the cells were cultured in serum-free medium for 24 h, followed by treatment with the indicated concentrations of each compound for 48 h. Cells were then washed with PBS and treated with MTT solution (final concentration, 5 mg/mL) for 3 h at 37 °C. The supernatant was removed, and the formazan crystals were dissolved in 100 µL of isopropanol. Absorbance at 540 nm was measured with a microplate reader VICTOR 3 Model (PerkinElmer, Waltham, MA, USA).
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