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Cck 8 assay kit

Manufactured by Transgene
Sourced in China

The CCK-8 assay kit is a colorimetric assay used to measure cell proliferation and cytotoxicity. It utilizes the water-soluble tetrazolium salt WST-8, which is reduced by cellular dehydrogenases to produce a colored formazan dye. The amount of formazan dye is directly proportional to the number of living cells, allowing for quantification of cell viability and proliferation.

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4 protocols using cck 8 assay kit

1

Cell Proliferation Evaluation via CCK-8 Assay

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Cellular proliferation was evaluated using the CCK-8 assay kit (Transgen, China). Cells were plated in 96-well plates at a concentration of 3 × 103 cells per well. Post-seeding, cells were incubated for specific durations:12, 24, 48, and 72 h. After each interval, CCK-8 reagent was added to the wells, and the plates were incubated at 37 °C for an additional 3 h. The optical density of each well was subsequently recorded at 450 nm using a microplate spectrophotometer.
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2

CCK-8 Assay for DCAF13 Impact

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A CCK-8 assay kit (TransGen Biotech # FC101-03, Beijing, China) was used to determine the effect of DCAF13 on cell proliferative abilities. Three siRNAs and siControl were transfected to knock down the expression of DCAF13 according to the manufacturer’s protocol. Cells were used for plate spreading 48 h after transfection. 2 × 10^3 transfected cells with 100 μl of culture medium were seeded and grown in 96-well plates, followed by incubation with CCK-8 solutions for 1 h at indicated periods (0, 2, 4, and 6 days). Subsequently, the absorbance value (450 nm) was measured using a microplate reader.
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3

Cell Proliferation Assay using CCK-8

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Cell proliferation was determined using the CCK 8 assay kit (Transgen, China). 96-well plates were seeded with 3 × 103 cells per well. The cells were cultured for 24, 48, 72 and 96 h before being treated with CCK8 at 37 °C for 3 h. The absorbance at 450 nm was measured using a microplate reader.
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4

Luteolin Cytotoxicity Assessment

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To measure luteolin cytotoxicity, MDCK (2.5 × 10 4 ), Vero (3 × 10 4 ) and Calu-3 (2 × 10 4 ) cells were grown in 96-well plates. After being cultured for overnight, cells were incubated with various concentrations of luteolin that ranged from 3.75 to 240 μM for an additional 48 h. Cell viability was measured using a CCK-8 assay kit (TransGen, Beijing, China) following the manufacturer's instructions. The absorbance of each well was recorded at 450 nm using a Multiskan MK3 microplate reader.
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