The process known as Polymerase Chain Reaction or PCR is a ubiquitous and simple procedure in molecular biology for augmenting DNA segments into a range of copies. It is essential not just for basic research, but also in forensics, medical and diagnostics applications.
Quantitative virtual PCR is an advanced version that includes fluorescencebranding to cumulatively calculate DNA amplification and not just than supervising it at the end of the procedure, as in traditional PCR. Existing PCR therefore allows sensitive quantification of the volume of the initial DNA template. But, present techniques may reveal bias through pipetting inaccuracies, sequence errors or disproportionate binding of fluorescent probes or hybridization.
A scientific team headquartered in Nagoya University has now introduced a new technique of estimating real-time DNA amplification that is label-free and thus avoids the bias troubles linked with other procedures.
Real-time label-free identification systems depend on surface immobilization of target molecules that is extremely costly, ineffective and laborious over-time. It is a novel technique that introduced an element of hybridization instead identifies alterations in the intensity of diffracted light from a beam of laser passing via miniscule 200 nm (0.0002 nm) – extensive nanochannels occupied with analytical sample liquids.
The 532-nm beam of laser is engrossed by a lens and then shifted by routing through the nanochannel and identified by a photodiode. The substrates if Silica were utilized to prepare the nanochannels and the bigger difference between refractive indices of silica and sample liquids, the smaller is the alteration in diffracted light intensity and vice versa.
“We utilized this procedure to offer the very first label-free identification of individual papillomavirus and the microorganism responsible for causing tuberculosis,’ says Takao Yasui, the first author of the report. “The technique is extremely sensitive and enables quantification of an extensive assortment of initial DNA concentrations, from 1 pm to 1 fM, so is bigger to the current fluorescence – based identification systems.”
“Our process also calculates DNA amplification at the moderately low temperature of 34 Degree Celsius without the requirement for thermal cycles,” says the co-author Noritada Kaji. “Since it has the ability to be constructed as a sole chip and can identify sample volumes as tiny as 1 ul, which is approximately 100 to 1000 times less than the traditional detectors are potential of, it is specifically ideal to the improvementas a miniaturized type of diagnostics and microbe detection.” In all, it appears a highly beneficial and a promising research for the diagnostics industry spanned across the world.
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