Difference between revisions of "SDx Protocol 1"
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#Withdraw 200 µL of the old test solution from the tethaPlate well. | #Withdraw 200 µL of the old test solution from the tethaPlate well. | ||
#Replace with 200 µL of the PBS buffer. | #Replace with 200 µL of the PBS buffer. | ||
| − | #Repeat | + | #Repeat steps 8 - 9 every minute three times, and observe whether the ionophore can be 'washed out'. |
Prepare a graph of conductivity vs log of ionophore concentration. | Prepare a graph of conductivity vs log of ionophore concentration. | ||
It is usual to find that there is a sudden rise in conductivity over a single decade of concentartion increase. If you want better resolution on your graph | It is usual to find that there is a sudden rise in conductivity over a single decade of concentartion increase. If you want better resolution on your graph | ||
Revision as of 18:29, 7 August 2013
Membrane formation
Assemble the tethaPlate as per its instructions. To each well add 8-10 µL AM199 lipid mixture, and incubate for 2 minutes to allow the phospholipid bilayer membrane to form. Now add 200 µL PBS per well followed immediately by three 200 µL PBS rinses.
Stock solution
Make a 1 mM stock solution of the ionophore in methanol. Using the method of serial dilution prepare a series of solutions in decade concentration increments, allowing 200 uL per test well so that you have solutions of 1, 10, 100, 1000, 10000 nM. The 10000 nM solution will still contain only 1% methanol, which means that the solution is mainly water. Higher methanol concentrations can disrupt the membrane, or allow incomplete partitioning of the ionophore into the lipophillic membrane.
If you need to use more concentrated test solutions then you will need to make a more concentrated stock solution (eg 10 or even 100 mM) and dilute these down to the desired levels.
Compound Addition
Ensure all solutions are thermally equilibrated at room temperature before starting.
Start recording with the tethaPlate fitted to the tethaPod unit, proceed for several minutes until stable baseline signals are obtained for each of the sample wells.
- Withdraw 200 µL of the PBS buffer from the tethaPlate well.
- Note the time and replace with 200 µL test solution at lowest concentration.
- Record the membrane conductivity for at least 5 minutes, or until the signal plateaus.
- Withdraw 200 µL of the old test solution from the tethaPlate well.
- Note the time and replace with 200 µL test solution at the next lowest concentration.
- Record the membrane conductivity for at least 5 minutes, or until the signal plateaus.
- Repeat from step 4 to step 6, until the highest concentrations ir reached (or until the membrane ruptures)
- Withdraw 200 µL of the old test solution from the tethaPlate well.
- Replace with 200 µL of the PBS buffer.
- Repeat steps 8 - 9 every minute three times, and observe whether the ionophore can be 'washed out'.
Prepare a graph of conductivity vs log of ionophore concentration.
It is usual to find that there is a sudden rise in conductivity over a single decade of concentartion increase. If you want better resolution on your graph
