Cut out the area with DNA in to as small a piece as possible. Put in an eppendorf. Add~50ul TE (or H2O). Use pipette tip to agitate paper and buffer. Remove 5ul buffer and transform bacteria. Make sure you use very clean scissors/ tweezers etc to prevent contamination.
Cut out the area with DNA in to as small a piece as possible. Put in an eppendorf. Add~50ul TE (or H2O). Use pipette tip to agitate paper and buffer. Remove 5ul buffer and transform bacteria. Make sure you use very clean scissors/ tweezers etc to prevent contamination.