Hi,
I'm an MD/PhD student at Northwestern. I recently learned about your smFISH technique from a Biosearch Rep at SfN this past week. I'm interested in attempting to use this technique to study neurons and neuron-like cells (SY5Y, NT2).
My lab currently has the right set-up for doing the imaging. However, we do not use LabTek chambers, but we instead always plate cells on coverslips in standard 6- or 12-well plates, and then mount the coverslips on standard slides for imaging. I would like having to avoid making an investment in LabTek chambers if possible.
Has anyone tried doing using coverslips on standard slides before with this technique? Are there any caveats/pitfalls with this protocol change that I should be careful about?
Thank you,
Warren