Advancing forensic RNA profiling: Preventing noise signals in RNA profiling by adding the multiplex buffer last  Margreet van den Berge, Titia Sijen 

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Advancing forensic RNA profiling: Preventing noise signals in RNA profiling by adding the multiplex buffer last  Margreet van den Berge, Titia Sijen  Forensic Science International: Genetics Supplement Series  Volume 5, Pages e518-e519 (December 2015) DOI: 10.1016/j.fsigss.2015.09.205 Copyright © 2015 Elsevier Ireland Ltd Terms and Conditions

Fig. 1 Overlay electropherograms. (A) A skin sample amplified showing background noise. Red marker bins indicate locations for which no signals are expected; light green marker bins those of skin and housekeeping markers. The bars below the green bins indicate the fluorophore colour of the expected signal. (B) Blank controls amplified after primer mix and multiplex buffer stood combined in concentrated (no water added) for 60, 12 or 0min. (C) Blank control amplified after primer mix and multiplex buffer were combined in diluted form (water added) for 60min. (D) Blank control amplified when the multiplex buffer was added last, and the PCR was started immediately. Forensic Science International: Genetics Supplement Series 2015 5, e518-e519DOI: (10.1016/j.fsigss.2015.09.205) Copyright © 2015 Elsevier Ireland Ltd Terms and Conditions