Cell Stimulation MIX Kit

Cell Stimulation MIX Kit

Introduction

Elabscience^® Cell Stimulation MIX Kit is a mixture of Phorbol 12-Myristate 13-Acetate (PMA) and Ionomycin, which can induce various cell activation and secrete cytokines. The activated cell supernatant can be used to detect cytokines by immunological methods. It is possible to add Protein Transport Inhibitor MIX [E-CK-A013] at an appropriate time to detect cytokines by flow cytometry.

Reagent Preparation

500×Cell Stimulation MIX: Add 100 μL Cell Stimulation MIX Solvent to dissolve a vial of Cell Stimulation MIX and mix fully.

Note: Centrifuge at 2000~10000×g for several seconds before use and then open the cover for use.

Experimental Procedure

Application 1: Cytokine content or activity detection in cell culture supernatant

1. Prepare the single cell suspension with complete medium (self-prepared), and adjust the cell density to 1~2×10⁶/mL.
   Note: The cell density should not be too high, and the maximum density should be less than 2×10⁶/mL, high cell density will affect cell activation efficiency. Make sure the cells are in good condition before stimulation, especially for freshly prepared primary cells.
2. Add 2 μL of 500× Cell Stimulation MIX to each 1 mL of cell suspension, and incubate the cells at 37°C, 5%CO₂ for 4~18 h (It is recommended to determine the optimal induction time by setting up a pre-experiment with different induction times for the cytokines to be tested. The common induction time can be refer to table 1).
3. Collect cell culture supernatant for the subsequent detection or store at -80°C for later use (the supernatant contains a variety of cytokines secreted by cells, which can be used to detect the content and activity of cytokines by ELISA or other biochemical reagents).

Application 2: Intracellular factor detection

1. Prepare the single cell suspension with complete medium (self-prepared), and adjust the cell density to 1~2×10⁶/mL.
   Note: The cell density should not be too high, and the maximum density should be less than 2×10⁶/mL, high cell density will affect cell activation efficiency. Make sure the cells are in good condition before stimulation, especially for freshly prepared primary cells.
2. Add 2 μL of 500× Cell Stimulation MIX to each 1mL of cell suspension, and incubate the cells at 37°C, 5%CO₂ for 1.5~1 h.
3. Add 1 μL of 1000×Protein Transport Inhibitor MIX [E-CK-A013] to each 1mL of cell suspension, and incubate the cells at 37°C, 5%CO₂ for 5~16 h (It is recommended to determine the optimal induction time by setting up a pre-experiment with different induction times for the cytokines to be tested. The common induction time can be refer to table 1).
4. Collect cell suspension, centrifuge at 200~300×g for 5 min, discard the supernatant and collect the cell pellet which could be used for subsequent intracellular factor detection after fixation.

Table 1: Reference of inducing condition of intracellular factors

Troubleshooting

Storage

1. Powder reagents can be stored for 1 year in the dark at -20°C and 2 years in the dark at -80°C.
2. The dissolved powder can be stored at -20°C for 6 months, or stored at -80°C for 1 year after subpackaged.

Notes

1. This kit is for research use only.
2. Due to the effect of Brefeldin A in Protein Transport Inhibitor MIX on CD69, it is recommended not to add Protein Transport Inhibitor MIX when detecting CD69. However, this operation may cause intracellular factors to be secreted outside the cell.
3. Please take safety precautions and follow the procedures of laboratory reagent operation.
4. Please store the product at the appropriate temperature to avoid failure.