生物
李子
等位基因
底漆(化妆品)
遗传学
基因分型
盐李
聚合酶链反应
放大器
种质资源
栽培
基因型
植物
基因
有机化学
化学
作者
B. G. Sutherland,Timothy P. Robbins,K. R. Tobutt,Wilhelm Weber
出处
期刊:Plant Breeding
[Wiley]
日期:2004-12-01
卷期号:123 (6): 582-584
被引量:94
标识
DOI:10.1111/j.1439-0523.2004.01016.x
摘要
Abstract Although various consensus polymerase chain reaction (PCR) primers have been reported for identifying Prunus S ‐alleles, they have been developed from and optimized on a limited set of alleles, which may limit their applicability to a broader allele range. To develop a primer set for use across the genus, degenerate consensus primers were designed from conserved regions of 27 S‐RNase sequences available from five Prunus species. The primers were tested in 15 previously genotyped cultivars of cherry, almond and apricot, representing alleles S 1 to S 6 in each crop and also S c in apricot. Comparisons were made with previously published primers tested in the same 15 cultivars under reported reaction conditions. The new primers generated an amplification product for each of the 19 S ‐alleles whereas those previously available amplified no more than 14. The primers will be useful for genotyping and genetic studies in cultivars and wild populations.
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