BODIPY 493/503 (Pyrromethene 546) is a lipophilic fluorescent probe with Ex/Em of 493/503 nm. BODIPY 493/503 localizes to polar lipids and can be used to label cellular neutral lipid contents and for live and fixed cell applications.

METHODS: Flow cytometry was used to detect cellular lipid droplets:
1. BODIPY 493/503 is dissolved in 5 mM DMSO stock solution and diluted 1:2500 in PBS to a 2 µM working solution prior to use.
2. Cultivate cells under culture conditions relevant to the study, e.g. 50,000 A498 cells in 35 mm wells. Overnight incubation of cells with 30 µM oleic acid serves as a positive control for increased neutral lipid content.
3. At the time point of interest, prepare a 2 µM BODIPY staining solution in PBS. The volume of staining solution required for each sample corresponds to the volume of medium used to incubate the cells.
4. Rapidly rinse the cells with 3 mL of PBS to remove the medium/serum. Incubate in BODIPY Staining Solution for 15 min at 37°C in the dark.
5. Rapidly rinse the cells with 3 mL of PBS to remove the staining solution. Trypsinize the cells to produce a single-cell suspension. Add 5 mL of PBS and transfer the cell suspension to a 15 mL conical tube.
6. Centrifuge cells at 250×g for 5 min at 4°C. Remove the supernatant, quickly rinse the cell sediment with 3 mL of PBS, and centrifuge again, 250 × g, 5 min, 4°C.
7. Remove the supernatant and resuspend the cells in 300 µL of 1× flow cytometry buffer for flow cytometry assay. [1]
METHODS: Fluorescent microscopy to detect cellular lipid droplets:
1. Dissolve BODIPY 493/503 into 1 mg/mL DMSO stock solution, and add 10 µL of 1 mg/ml BODIPY 492/503 stock solution to 10 mL of 150 mM NaCl to prepare a working solution before use.
2. One or two days before staining, culture the cells on sterile glass coverslips. Plate the cells at 50%-70% fusion to keep them semi-fused during staining.
3. To enhance lipid droplet formation and facilitate detection, supplement cell growth medium with 400 µM sodium oleate for 6-24 h prior to fixation and lipid droplet staining.
4. Rinse cells twice with 2 mL of PBS. Fix cells by incubating with 2 mL of 3% (w/v) paraformaldehyde for 30 min at room temperature.
5. Rinse the cells three times with 2 mL PBS. Cells were covered with 1 mL of BODIPY 493/503 working solution and incubated for 10 min at room temperature, protected from ambient light.
6. Wash cells three times with 2 mL PBS. Mount coverslips onto slides using 20-40 µL of anti-fade mounting medium.
7. Detect BODIPY 493/503 staining of lipid droplets using fluorescence microscopy.

The above information is based on published literature. Experimental procedures should be appropriately modified to meet specific research demands.

I. Flow cytometry detection of cell lipid droplets:
1. Dissolve BODIPY 493/503 into a 5 mM DMSO stock solution and dilute it to a 2 µM working solution at 1:2500 with PBS before use.
2. Culture cells under culture conditions relevant to the study, such as 50,000 A498 cells in a 35 mm well. Overnight incubation of cells with 30 µM oleic acid can serve as a positive control for increased neutral lipid content.
3. At the time point of interest, prepare a 2 µM BODIPY staining solution in PBS. The volume of staining solution required for each sample corresponds to the volume of culture medium used to culture cells.
4. Quickly rinse cells with 3 mL PBS to remove culture medium/serum. Incubate with BODIPY staining solution for 15 min in the dark at 37°C.
5. Quickly rinse cells with 3 mL PBS to remove staining solution. Trypsinize cells to produce a single cell suspension. Add 5 mL PBS and transfer the cell suspension to a 15 mL conical tube.
6. Centrifuge the cells at 250×g for 5 min at 4°C. Remove the supernatant, quickly rinse the cell pellet with 3 mL PBS, and centrifuge again at 250×g for 5 min at 4°C.
7. Remove the supernatant and resuspend the cells in 300 µL 1× flow cytometry buffer for flow cytometry detection. [1]
II. Fluorescent microscopy to detect cell lipid droplets:
1. Dissolve BODIPY 493/503 into a 1 mg/mL DMSO stock solution. Before use, add 10 µL of 1 mg/ml BODIPY 492/503 stock solution to 10 mL of 150mM NaCl to prepare a working solution.
2. One or two days before staining, culture the cells on sterile glass coverslips. Plate cells at a confluency of 100 μL and keep them semi-confluent during staining.
3. To enhance lipid droplet formation and facilitate detection, supplement cell growth medium with 400 μM sodium oleate for 6-24 h before fixation and lipid droplet staining.
4. Rinse cells twice with 2 mL PBS. Fix cells by incubating with 2 mL 3% (w/v) paraformaldehyde for 30 min at room temperature.
5. Rinse cells three times with 2 mL PBS. Cover cells with 1 mL BODIPY 493/503 working solution and incubate at room temperature for 10 min, protected from ambient light.
6. Wash cells three times with 2 mL PBS. Mount coverslips onto slides using 20-40 μL antifade mounting medium.
7. Detect BODIPY 493/503 staining of lipid droplets using fluorescence microscopy.

The above information is based on published literature. Experimental procedures should be appropriately modified to meet specific research demands.

DMF: Soluble

Chloroform: Soluble

Methanol: Soluble

Ethanol: 0.24 mg/mL (0.92 mM), Sonication is recommended.

DMSO: 2.00 mg/mL (7.63 mM), Sonication is recommended.