Utilised to separate and isolate DNA fragments based on their size (length/number of bases)
An agarose gel is prepared and loaded into a gel tank filled with a buffer solution and connected to a power supply. DNA fragments are mixed with loading dye and pipetted into the wells.
A DNA ladder sample is placed in the first lane. This contains DNA fragments of known sizes to compare and help estimate the size of DNA fragments in various samples.
An electric current is applied causing the smaller fragments to travel further and faster through the gel than longer fragments. After a certain time, the gel is viewed under UV light.