Hi all,

I am facing some practical issues in subculturing of the SH-SY5Y human Neuroblastoma cell line.

I've already followed the protocol related to differentiation of the SH-SY5Y human Neuroblastoma cell line, however, the number of attached cells in the plates after transferring the cells to the new plates and changing media with differentiation Media #2 become decreased significantly and have not improved yet.

I would like to know that can I make a modification in the protocol and keep the cells for more days in the same plates and do not transfer them to the new Poly-D-Lysine coated plates based on the protocol? or I have to follow the protocol exactly step by step?

My concern is that after using Trypsin 1X, and transfer cells to the fresh plate, I will loss all of remaining attached cells.

I am Looking for experts advice on handling of this issue. Thank you.

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