Hello,
I ran RFLP gel where I noticed that the ladder ran faster than the sample. When the ladder dye crossed the plate, I took the gel out and visualized. Now, I don't understand why this happened. I followed our standardized protocol. I ran this gel for other samples before and it came out well.
Please suggest what might have went wrong, Is it with gel composition or something else.
I diluted the ladder with loading dye and water (as per the protocol) and kept at 4degree a day before. Can this be an issue? Please suggest.