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Hello Why I am getting a red dot( or false satining)when I stain my primary cultures only with DAPI?This spots looks red in DAPI filter and looks green in FITC filter and red in TRITC filter...
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Can somebody share a protocol on how to do Environmental Scanning Electron microscopy on culture cells grown on silicon chips. I want to do immuno labelling in SEM using gold label secondary...
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thankyou for your help
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