In gel electrophoresis, the anode is positively charged. DNA is a negatively charged molecule, which attracts different charges, so DNA migrates towards the anode during gel electrophoresis.
Gel electrophoresis is the experimental method for the separating mixtures of the DNA, RNA, or the proteins by the molecular size. In gel the electrophoresis, the molecules to be separated are to be forced into the gel containing small pores by the electric field. What is the Principle of Gel Electrophoresis? Gel Electrophoresis and DNA DNA is negatively charged, so when an electric current is passed through the gel, the DNA migrates towards the positively charged electrode. Fragments are ordered by size because short DNA strands migrate through the gel faster than long strands.
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