|Product name||MTT-Cell Based Proliferation/Toxicity Assay Kit|
Measurement of cell viability and proliferation forms the basis for numerous in vitro assays of a cell population’s response to external factors. The reduction of tetrazolium salts is now widely accepted as a reliable way to examine cell proliferation. The key substrate of the kit is: 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide or MTT. MTT is a yellowish solution when dissolved in balanced salt solutions without phenol red and is taken up by cells due to its net positive charge. The tetrazolium ring of MTT (yellow) is reduced to purple formazan crystals by intracellular NAD(P)H-oxidoreductases. The formazan crystals are insoluble in aqueous solution, but become solubilized in the provided Solubilization Buffer. After solubilization, the resulting purple solution is spectrophotometrically measured. The MTT Cell Proliferation Assay measures the cell proliferation rate and conversely, when metabolic events lead to apoptosis or necrosis, the reduction in cell viability. The number of assay steps has been minimized as much as possible to expedite sample processing. The MTT Reagent yields low background absorbance values in the absence of cells. For each cell type the linear relationship between cell number and signal produced is established, thus allowing an accurate quantification of changes in the rate of cell proliferation.
|Materials Required but Not Supplied|
|Procedure: 96 Well Format||If you are familiar with the procedure and know the cell count to use in your specific assay, you may follow this basic protocol.|
Seed cells in a 96-well plate at a density of 2000 cells/well (for proliferation Assay ) or 5000 cells/well (Toxicity Assay ) in 100 ul of culture medium (depending on cell type)
Incubate for appropriate time according to the experiments and treated with the substance to be assayed.
Add 10 μl MTT Reagent
Incubate the cells for 3-4 hours in the incubator. Dark brown formazan crystals are formed in the cells. For higher cell density, the incubation time can be shortened accordingly.
Add 100 μl Formazan Dissolving Solution.
Incubate for about 4 hours at 37°C when the purple precipitate is absolutely dissolved.
Record absorbance at 560-600 nm.Note:
Due to the use of 96 - well plates for testing, if the cells are cultured for a long time, the problem of evaporation should be attention. On the one hand, because a circle around the orifice of 96 well is the most easy to evaporate, the circle around can be deprecated or use PBS, water or nutrient solution; On the other hand, the 96 plates can be placed near the water in the cabinet, to alleviate the evaporation.
If the Formazan is frozen or produce precipitation, 56 ℃ water bath can be maintained to promote dissolving, and must be used after dissolving and blending absolutely.
MTT solution is yellow, need to avoid light preservation, long light can lead to failure. When the color turned into a sage green, it would not be used.
|Performing an assay||The plot of the data obtained in Step 7(absorbance against number of cells) should provide a curve with a linear portion. The optimal number of cells for the assay should fall within the linear portion of the curve and give an absorbance value between 0.75 and 1.25.Then both stimulation and inhibition of cell proliferation can be measured. For best results, cells in log phase of growth should be employed and the final cell number should not exceed 106 cells/cm2 Each experiment should include a blank containing all of the reagents in a well without cells. Assays will include:|
Blank wells containing medium only.
Untreated control cells.
Test cells treated with the substance to be assayed.If more than 100 μl of medium is used per well, increase the amount of MTT Reagent accordingly; e.g., for 250 μl of medium use 25 μl of MTT Reagent.
|Data interpretation||Absorbance values that are lower than the control cells indicate a reduction in the rate of cell proliferation. Conversely a higher absorbance rate indicates an increase in cell proliferation. Rarely, an increase in proliferation may be offset by cell death; evidence of cell death may be inferred from morphological changes.|