Estrogen Receptor-Reporter Activity Assay to Screen Phytoestrogen Estrogenic Activity
DEŞİFRE METNİ
Vortex the samples. Then, add 4 microliters of each sample to 496 microliters of compound-screening medium, to yield a 0.8% DMSO solution.
Disinfect the outside surface of a pre-warmed cell recovery medium tube with 70% ethanol, and transfer 10 milliliters of the medium into a tube of frozen reporter cells to thaw them. Close the tube of reporter cells, and place it in a 37-degree Celsius water bath for 5 to 10 minutes.
After retrieving the cells from the water bath, gently invert the tube several times to break up aggregates of cells, and produce a homogeneous suspension. Then, clean the surface of the tube with 70% ethanol.
Use a multi-channel pipette to dispense 100 microliters of the reporter cell suspension into each well of a 96-well plate. Then, dispense 100 microliters of samples in triplicate into the appropriate wells. Incubate the plate at 37 degrees Celsius and 5% carbon dioxide for 22 to 24 hours.
Just prior to the end of the plate incubation, remove detection substrate and detection buffer from the refrigerator, and place them in a low-light area until equilibrated to room temperature. Then, gently invert each tube to mix the solutions.
Immediately before the plate incubation is complete, pour the entire contents of the detection buffer into the tube of detection substrate, to create luciferase detection reagent. Mix the tube gently, so as not to produce foam.
Discard the contents of the sample plate into an appropriate waste container, and gently tap it on a clean absorbent paper towel to remove the last droplets from the wells. Add 100 microliters of the luciferase detection reagent to each well, and allow the assay plate to rest at room temperature for 15 minutes. Then, quantify the luminescence using a 96-well-plate-reading luminometer.
