I need to show stability of my gene delivery vector against cellular DNase. I tried the gel electrophoresis method but it is not working. Kindly suggest an alternative.
If your vector is damaged by the DNase action, you'll see different melting peaks or a different melting point . Melting analysis is a common procedure for qPCR customers. You only have to mix your product with the appropriate amount of dye and program an standard meeting analysis in your qPCR instrument.