It was until the beginning of the last 2 decades that Kary Mullis broke the silence among the scientists with the revolution of even more sophisticated device into our diagnostics laboratories. Before this invention, the diagnostics tools were very limited to conventional methods and these had created our inability to detect many viable but non-culturable pathogens. These days, both of Norovirus and Treponema pallidum can be diagnosed in the clinical laboratories without the use of electron microscope (EM) and culture plate methods respectively [1,2].Polymerase Chain Reaction is a deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) in a form of complimentary DNA (cDNA) amplification machine that can detect even the smallest amount of DNA present in the targeted cell or organism. The machine works with the principles of a thermostable DNA polymerase and this eliminate the use of olden system of water bath. Thermus aquaticus is a bacterium that can withstand the heat that provides the optimum temperature for the double stranded DNA to be unwound or denature into single stranded and be ready for the alignment of the nucleotide base sequences. The sensitivity and specificity of these methods laid its foundation and made it winning the upper handIn recent days; the mainstay of medical management and control of diseases (epidemiology) is in the hands of quantitative PCR.The detection of chronic viral infections and fastidious organisms and the accurate detection of an inflammatory bowel disease and bacterial vaginosis brought even more confidence to the research scientists [4,5].With the advent of series of PCR types that includes the quantitative real time PCR, the sectors such as food engineering, diagnostics laboratories (both clinics and research), forensic, genetics and infectious diseases, agricultural production, human genome sequencing projects and the list continues all experienced an overwhelming improvement. The old problematic adage that goes with the hypothesis that; drug-resistant tuberculosis or ventilator-associated pneumonia was difficult to be detected has surrendered to the quantitative PCR and in a real time [5]. In addition to discriminating DNA, in microarray research sectors and qPCR has been widely used for validating expression of miRNAs in whole genome analyses [6,7].Real time here implies that even during the reaction, the amplification and analysis as well is ongoing. This is the simultaneous advantages found in real time over conventional PCR that will only enable end product analysis by gel electrophoresis. While the conventional PCR relied on the end point analysis can be analyzed based on the base pair (bp) seen on the agar gel electrophoresis, real time PCR has its reaction on amplifying and analyzing the am-