Amplite® Colorimetric Beta-Galactosidase Assay Kit

1. Prepare stable or transient transfected cells with LacZ gene
2. Incubate cells (samples) with test compounds
3. Lyse the cells
4. Transfer the lysate to a microtiter plate
5. Add FDG working solution
6. Incubate at room temperature or 37°C for at least 5 minutes depending on cell type
7. Add stopping solution
8. Measure the OD ratio at the wavelength of 580 nm to 460 nm (Ab₅₈₀/Ab₄₆₀)

Thaw all the kit components to room temperature before use.

For guidelines on cell sample preparation, please visit https://www.aatbio.com/resources/guides/cell-sample-preparation.html

Unless otherwise noted, all unused stock solutions should be divided into single-use aliquots and stored at -20 °C after preparation. Avoid repeated freeze-thaw cycles

Add 50 µL of DMSO (Component E) into the vial of Resorfuin β-D-Galactosidase (Component A) to make 200X Resorufin β-D-Galactosidase stock solution.

Note: 25 µL of this stock solution is enough for one 96-well plate. Keep from light.

Add 30 µL of β-mercaptoethanol (Component F) to 10 mL of Reaction Buffer (Component B), and mix well.

Note:Additional buffer is needed for preparing enzyme dilution buffer, which is used to generate a standard curve.

Add 25 µL of Resorufin β-D-Galactosidase stock solution (200X) into 5 mL of 0.3 % β-mercaptoethanol assay buffer.

Note:This working solution is enough for one 96-well plate.

Add 5 µL of β-mercaptoethanol (Component F) to 5 mL of Lysis Buffer (Component D) before use.

Note: Always add 0.1% β-mercaptoethanol into lysis buffer before lysing the cells.

Table 1. Recommended Lysis Buffer working solution volumes for cell culture plates.

1. Treat cells containing LacZ gene with test compounds for a desired period of time.
2. Wash the cells twice with 1X PBS. Do not dislodge the cells.

3. Lyse cells accordingly with Lysis Buffer working solution.

   For adherent cells: Add Lysis Buffer working solution to the culture plates. See table 1 for recommended volumes.

   For non-adherent cells: Pellet the cells into centrifuge tube, and add 50 - 2000 µL (depending on the size of the cell pellet) of Lysis Buffer working solution to the tube.

4. Incubate cells from previous step at room temperature for 10 - 15 minutes, and gently swirl the plates or tubes several times to ensure complete lysis.

5. Proceed to the β-galactosidase assay or freeze the sample at -80 °C until use.
   
   Note: A good lysis can also be obtained by a quick freeze-and-thaw cycle (freeze 1 - 2 hours at -20°C to -80°C and thaw at room temperature). Alternatively, centrifuge the cell lysis for 2 - 3 minutes to pellet the insoluble material, and then assay the supernatant.

1. Thaw the tube or plate of lysed cells at room temperature if needed. Perform the assay directly on the 96-well plate if the cells were seeded in a 96-well plate.

2. Add 50 µL of cell extracts into each well of the 96-well plate. Save some control wells for the standard curve (50 uL/well) if a standard curve is desired.
   
   Note: If necessary, dilute the lysate in Lysis Buffer working solution when transfection efficiency is very high or reduce the volume of lysis buffer when transfection efficiency is low. If the transfection is performed in a 96-well plate, or a stable cell line was seeded into a 96-well plate, perform the assay directly on the plate. For endogenous β-galactosidase activity control, add 50 µL of cell lysate from non-transfected cells. For blank control, add 50 µL of Lysis Buffer working solution.

3. Add 50 µL of Resorufin βDG working solution to each well. Incubate the plate at room temperature or 37°C for approximately 10 min to 4 hr depending on the cell type.
4. Add 50 µL of Stop Buffer (Component C) to each well.
5. Monitor the absorbance increase by measuring the OD ratio at the wavelength of 580 nm to 460 nm (Ab₅₈₀/Ab₄₆₀) using an absorbance microplate reader.