Hi
I am trying to extract RNA from Fibrin gels for qPCR and subsequently RNA sequence. My gels are small volume (250ul).
I have had significant issues with getting high values for ng/ul for these gels using a variety of extractions - Trizol, Dispase then Trizol, Dispase then Trizol the chloroform.
The gels seem not fibrous enough to warrant homogenisation (I attempted this and it didn't seem to improve anything). The quality of the gels is fine, just not the Quantity of the RNA.
Does anyone have any similar experiences or useful protocols they may be able to share to help with this?
With Best Wishes
Rob