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For instance, if I do serial dilution of microbiology culture with 10^-6 with (100/900 microliter) in place of 1mL/9mL volumes, is it acceptable or is it a bad practise?
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I am aware that ellipsometry, OWLS and QCM are some of the methods. Which will be the suitable method to analyze the deposition profile? Also, can I carry out analysis on the textile fabric?
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