2004
DOI: 10.1016/j.forsciint.2003.10.008
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Real-time PCR designs to estimate nuclear and mitochondrial DNA copy number in forensic and ancient DNA studies

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Cited by 167 publications
(127 citation statements)
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“…[10][11][12][13] DNA was extracted from 200 mL of unfractionated sample by using the Plasma-9 Serum Circulating DNA Purification Mini kit (catalog number 50600; Norgen Biotek, Thorold, Ontario, Canada) according to published methods. 7 DNA was eluted in 100-mL final volume and stored at 220°C.…”
Section: Real-time Polymerase Chain Reactionmentioning
confidence: 99%
“…[10][11][12][13] DNA was extracted from 200 mL of unfractionated sample by using the Plasma-9 Serum Circulating DNA Purification Mini kit (catalog number 50600; Norgen Biotek, Thorold, Ontario, Canada) according to published methods. 7 DNA was eluted in 100-mL final volume and stored at 220°C.…”
Section: Real-time Polymerase Chain Reactionmentioning
confidence: 99%
“…13 We used iQ SYBR Green Supermix (BioRad) in a iCycler Thermal Cycler (BioRad). Primers and thermal cycling conditions were as previously specified.…”
Section: Real-time Pcr Quantificationmentioning
confidence: 99%
“…The primer sequences for the small fragment were: L16001 ACCATTAGCACCCAAAGCTAAGA and H16065 GCGGTTGTTGATGGGTGAGT, and for the larger one: L16088 TCACCCATCAACAACCGCTAT and H16344 GGGACGAGAAGGGATTTGACT. The probe oligonucleotide sequence for the small fragment was FAM-CAAGCAAGTACAGCAA-MGB and for the large was VIC-GAAGCAGATTTGGGTAC-MGB (Alonso et al 2004). Real-time PCR amplification was performed in a 20µl reaction with 1x reaction TaqMan Universal PCR Master Mix (Applied Biosystem), 0,5 µM each primer, 50nM probes, 1mg/ml BSA and 1 µl DNA extract.…”
Section: Quantitation Of Number Of Dna Template Moleculesmentioning
confidence: 99%