Figure 1From: Multiplex qPCR for reliable detection and differentiation of Burkholderia mallei and Burkholderia pseudomallei Effect of increasing amounts of internal control on qPCR detection. A concentration range of genomic DNA from B. thuringiensis was mixed with a constant and low concentration of 14 fg B. mallei gDNA (A) or 48 B. pseudomallei DNA (B), and measured by using the developed multiplex qPCR.Back to article page