2014
DOI: 10.1007/s12686-014-0221-9
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Development of 21 microsatellite primers for Camellia pingguoensis (Theaceae) using 454 sequencing

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“…Microsatellite markers were selected from previously developed microsatellites in Camellia pingguoensis D. Fang ( Lu et al., 2014 ) and Camellia flavida H. T. Chang ( Liufu et al., 2014 ). PCR amplification was carried out in 20 μL reactions containing 2 μL 10 × PCR buffer (Mg 2+ plus), 0.4 μL dNTP mix (10 mM), 0.2 μL each primer (50 μM), 0.2 μL rTaq DNA Polymerase (all reagents from TaKaRa, China), 1.0 μL DNA (20 ng) and 16 μL double-distilled water.…”
Section: Methodsmentioning
confidence: 99%
“…Microsatellite markers were selected from previously developed microsatellites in Camellia pingguoensis D. Fang ( Lu et al., 2014 ) and Camellia flavida H. T. Chang ( Liufu et al., 2014 ). PCR amplification was carried out in 20 μL reactions containing 2 μL 10 × PCR buffer (Mg 2+ plus), 0.4 μL dNTP mix (10 mM), 0.2 μL each primer (50 μM), 0.2 μL rTaq DNA Polymerase (all reagents from TaKaRa, China), 1.0 μL DNA (20 ng) and 16 μL double-distilled water.…”
Section: Methodsmentioning
confidence: 99%