Why can I not see bands in my agarose gel after running my PCR product of sediment DNA?

crude DNA was1:10 diluted and used as template for PCR in a 50uL mixture and 4uL of the amplified product was mixed with 1uL of 6x gel loading buffer and run in a 0.8% agarose gel using 1x TE...

03 June 2015 1,355 10 View