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Methyl thiazolyl tetrazolium (mtt)

Manufactured by Bioswamp
Sourced in China

MTT is a colorimetric assay used to measure the metabolic activity of cells. It is a widely used method for determining cell viability, proliferation, and cytotoxicity.

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2 protocols using methyl thiazolyl tetrazolium (mtt)

1

MTT Assay for Cell Viability

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Cells were seeded in 96-well plates at 2 × 103 cells per well. 20 μL of MTT (5 mg/mL) solution (Bioswamp, Wuhan, China) was added to each well, and the cells were incubated for 0, 12, 24, 48, or 72 h. Then, the medium was removed, and 150 μL of dimethyl sulfoxide (Sigma, CA, USA) was added into each well. After fully mixing, the optical density was measured at 490 nm using a plate reader (Multiskan FC, Thermo, Massachusetts, USA).
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2

MTT Assay for Cell Viability

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The cells in logarithmic phase were collected and the concentration of the cell suspension was adjusted. The cells were inoculated into 96-well plates at a density of 5 × 10 3 cells per well, allocating 180 µL to each well. We set up three replicate wells for each subgroup. The cells were cultured overnight in a 37 °C, 5% CO 2 incubator to facilitate cell adhesion to the well walls. Following this, the culture plate was removed and added 20 µL MTT (5 mg/mL, batch number: C1736, Bioswamp, Wuhan, China) to each well, continuing the culture for an additional 4 hours. After removing the culture medium, 150 µL dimethyl sulfoxide (DMSO) (batch number: D2650, Sigma-Aldrich, St. Louis, MO, USA) was added to each well, shaking at a low speed for 10 minutes. Lastly, the optical density (OD) value was measured at a wavelength of 490 nm, using an enzyme labeling instrument (batch number: AMR-100, Allsheng, Hangzhou, China).
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