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Questions related from Michael Jeffrey Cimorelli
I am trying to image liposomes in a confocal and EPI fluoroscence wide-field microscope. I have labeled two species of interest and when I tried to image them and capture images, I had...
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I am working with samples that are approximately 10-12.5 mL after preparation of vesicles ranging in size from 400 nm to 6 um. I believe I have different structures being formulated that is...
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I have several microscope images taken from a confocal microscope that I plan to analyze further, but I was wondering if anyone had suggestions on how to enhance the image quality with an online...
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