Internal Validation Guide of the Amp F_STR Identifiler PCR by Using Quantifiler™ Y Human Male DNA Quantification for Use Forensic Laboratories
Author(s) -
Mohammed Mahdi Al–Zubaidi
Publication year - 2015
Publication title -
journal of al-nahrain university-science
Language(s) - English
Resource type - Journals
eISSN - 2519-0881
pISSN - 1814-5922
DOI - 10.22401/jnus.18.4.15
Subject(s) - buccal swab , genomic dna , chromatography , forensic genetics , dna extraction , microbiology and biotechnology , dna , biology , polymerase chain reaction , analytical chemistry (journal) , chemistry , genetics , allele , gene , microsatellite
Fifty samples of buccal swabs were collected from male oral cavity, then genomic DNA was extracted from each sample by two methods, the manual organic phenol chloroform methods and prepfiler forensic extraction kit methods.The concentration of genomic DNA extracted was measured by using Quantifiler® Duo Kit throughout detection the SRY (FAM™-labeled probe), RPPH1(VIC®-labeled probe) and an Internal Positive Control-IPC (NED™-labeled probe).Results showed that the concentration of genomic DNA in buccal swab was ranged between 0.26 and 9.422 ng/ul. these samples work with a serial dilution decimal, as well as PCR .Then introduced to the device 3130xl Genetic Analyzer 16-capillary array system, The results showed that the concentrations is preferable which is located between 25-50 pg, as this did not appear in the concentrations of any problems and the emergence of the peaks clearly Compared with the ALLELIC ladder and positive control, After the election concentrations were chosen Thresholds, Peak amplitude thresholds.
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