Efficient Amplification of Purified DNA with Ready PCR Mix
Figure 1. Single copy targets were amplified from 50ng of pUC19 plasmid (A) or S. aureus genomic DNA (B) for 35 cycles. 10μl of each PCR reaction was directly loaded onto a 1% agarose gel and visualized with a Syngene HR gel doc system.
Direct Colony Screening with Ready PCR Mix
Figure 2. 10 distinct colonies were suspended into Ready PCR Mix in separate PCR tubes. 5 μl of the PCR reaction mix was plated on gridded LB plates with Kanamycin for 37ºC overnight growth. After 30 PCR cycles products were screened on a 1% agarose gel. Colonies 4, 8, 9 and 10 contained the desired sequences. Courtesy of Dr. Irene Lee, Case Western Reserve University, Cleveland, OH
DNA Amplification by Ready PCR Mix Outperforms a Competitor Master Mix
Figure 3. Amplification products from AMRESCO Ready PCR Mix (Lanes 5-8) and a competitor master mix (Lanes 1-4) were resolved on a TAE/1.5% agarose gel containing Ethidium Bromide. Ethidium Bromide was included in the gel to visualize the products from the competitor master mix which lacks a DNA dye. Lanes 1, 2, 3: Aliquots (5 µl) from triplicate reactions with competitor master mix. Lanes 5,6,7: Aliquots (5 µl) from triplicate reactions with AMRESCO Ready PCR mix. Lanes 4 & 8: Non-template controls (5 µl) from competitor master mix and AMRESCO Ready PCR mix respectively. Data courtesy of Norgen Biotek Corporation.