04-22-2015, 07:09 PM
Hello Amoeba,
I think before running gel electrophoresis, you should quantify DNA for each sample along with the negative control. Also, take blank buffer/distilled water as a negative control. For samples, showing negative for DNA, you can take more number of colonies, to ensure sufficient amount of DNA extraction.
--AD
I think before running gel electrophoresis, you should quantify DNA for each sample along with the negative control. Also, take blank buffer/distilled water as a negative control. For samples, showing negative for DNA, you can take more number of colonies, to ensure sufficient amount of DNA extraction.
--AD