Recovery of genomic DNA from archived PCR product mixes for subsequent multiplex amplification and typing of additional loci: Forensic significance for older unsolved criminal cases

Journal of Forensic Sciences

Volumn 47, Issue 4, 2002, Pages 786-796

  Patchett, K L ^a   Cox, K J ^a   Burns, D M ^b  

^a Queensland and Scientific Services   (Australia)

^b GRIFFITH UNIVERSITY   (Australia)

Author keywords

Amelogenin; CSF1PO; D13S317; D18S51; D1S80; D21S11; D3S1358; D5S818; D7S8; D7S820; D8S1179; DNA typing; F13A; FES; FGA; Forensic science; Gc; Genomic DNA; GYPA; HBGG; HLA DQA1; LDLR; Multiplex amplification; Polymerase chain reaction; Short tandem repeat loci; THO1; TPOX; vWA

Indexed keywords

GENOMIC DNA;

CONFERENCE PAPER; CRIMINOLOGY; DNA FINGERPRINTING; ELECTROPHORESIS; GENE AMPLIFICATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 0036317885     PISSN: 00221198     EISSN: None     Source Type: Journal    
DOI: 10.1520/jfs15444j     Document Type: Conference Paper

References (4)

1. A method for the purification and recovery of genomic DNA from an HLA DQA1 amplification product and its subsequent amplification and typing using the Amplitype® PM PCR amplification and typing kit
2. Sequential multiplex amplification: Utility in forensic casework with minimal amounts of DNA and partially degraded samples
3. The re-use of genomic DNA remaining after PCR
4. Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material