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PrestoBlue™ Cell Viability Reagent Protocol

2019.4.22

实验概要

PrestoBlue™ Cell  Viability Reagent is a ready‐to‐use reagent for rapidly evaluating the  viability and proliferation of a wide range of cell types. PrestoBlue™  reagent is quickly reduced by metabolically active cells, providing a  quantitative measure of viability and cytotoxicity in as little as 10  minutes. Protect reagent from long term exposure to light and avoid  contamination, as this can reduce sensitivity.

实验步骤

1. PrestoBlue™  Cell Viability Reagent is supplied as a 10X solution. Add PrestoBlue™  Reagent directly to cells in culture medium. See below for example  volumes:

Format

Volume of cells   media

Volume of PrestoBlue™ Reagent

Cuvette

900 μL

100 µL

96-well plate

90 µL

10 µL

384-well plate

36 µL

4 µL

Note: Correct for background fluorescence by including control wells  containing only cell culture media (no cells) on each plate.

2. Incubate ≥10 minutes at 37º C. Longer incubation times will  increase sensitivity of detection. As this is a live cell assay,  readings may be taken at multiple time points to determine optimal  performance in your lab.

Format

Recommended Incubation Time

Bottom-read fluorescence

10 minutes – 2 hours

Top-read fluorescence

30 minutes – 2 hours

Absorbance

20 minutes – 2 hours

Room temperature incubation

10 minutes – 2 hours

Low cell number (< 5,000 cells/100 µL)

20 minutes – 24 hours

3. Read fluorescence or absorbance. Fluorescence is more sensitive than absorbance and is the preferred detection method.

Format

Excitation

Emission

General

540–570 nm

580–610 nm

Fluorescence
(Monochrometer)

560 nm (10 nm bandwidth)

590 nm (10 nm bandwidth)

Fluorescence (Filter)

535 nm (25 nm bandwidth)

615 nm (10 nm bandwidth)

Absorbance

570 nm

600 nm (reference wavelength for
normalization)

4. Calculate and plot the results. Higher fluorescence or absorbance values correlate to greater total metabolic activity.

Format

Instructions

Fluorescence

l  a. Optional: Average the fluorescence values of the no-cell control wells and
subtract from the fluorescence value of each experimental well.

l  b. Plot fluorescence vs. experimental condition (cell number, compound
concentration).

Absorbance

l  a. Normalize the 570 nm values to the 600 nm values for the experimental wells.

l  b. Plot the normalized 570 nm absorbance values vs. experimental condition (cell
number, compound concentration).


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