I want to measure ATP release ex vivo, but fear that ATP is broken down too quickly. Any experiences? Thanks!
You can inhibited enzyme degradation of ATP by adding EDTA. Whether your cells will stand this treatment I don't know. If not you have to separate the cells by centrifugation or filtration. Good luck!
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I want to apply fluids to ex vivo samples and measure ATP in them after some time. I was wondering if I can heat the fluid samples after taking them off the tissue to say 70 deg C, to inactivate...
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I want to shake cells to mechanically stimulate ATP release, but am afraid that some cells will burst. Is there a good test to check the supernatant afterwards for that?
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How to calculate the RMSD values for a MD simulation using MOE?
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