Fluo-3AM (solution)

Guide (The following is our recommended protocol. This protocol is only a guide and should be modified according to your specific needs).
1. Preparation of Fluo-3 AM working solution
1.1 Preparation of Fluo-3 AM working solution
Dilute the stock solution in HBSS to obtain 1-10 μM of working solution.
Note: Please adjust the concentration of Fluo-3 AMworking solution according to the actual situation.
2. Cell staining
2.1 Suspension cells (6-well plate)
2.1.1 Centrifuge at 1000 g at 4°C for 3-5 minutes and then discard the supernatant. Wash twice with PBS, 5 minutes each time. The cell density is 1×10⁶/mL
2.1.2 Add 1 mL of working solution, and then incubate at room temperature for 5-30 minutes.
2.1.3 Centrifuge at 400 g at 4°C for 3-4 minutes and then discard the supernatant.
2.1.4 Wash twice with PBS, 5 minutes each time.
2.1.5 Resuspend cells with serum-free cell culture medium or PBS. Observation by fluorescence microscopy or flow cytometry.
2.2 Adherent cells
2.2.1 Culture adherent cells on sterile coverslips.
2.2.2 Remove the coverslip from the medium and aspirate excess medium.
2.2.3 Add 100 μL of working solution, gently shake it to completely cover the cells, and then incubate at room temperature for 5-30 minutes.
2.2.4 Wash twice with medium, 5 minutes each time. Observation by fluorescence microscopy.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.