02 February 2019 3 4K Report

I have prepared a fungal suspension by scrapping out the fully grown fungal culture from the agar plate and homogenised them. i refered some of the literatures where they have used McFarland turbidity standard, 0.4 OD at 450 nm, 0.6 OD at 600m, 0.5 OD all these. can someone help me with this. what is the best way to optimise the initial inoculum before beginning the assay ?

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