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普通荞麦染色体的原位PCR技术研究 被引量:2
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作者 李分龙 陈庆富 《安徽农业科学》 CAS 北大核心 2011年第17期10135-10138,共4页
[目的]探索一种适合荞麦的简单易行的染色体原位PCR技术。[方法]采用16S套式引物、4.5S套式引物与psbA引物,以栽培甜荞为材料,进行染色体原位PCR、原位套式PCR与多次原位PCR试验。[结果]高温干燥可以起到与包埋类似的作用;染色体的原位... [目的]探索一种适合荞麦的简单易行的染色体原位PCR技术。[方法]采用16S套式引物、4.5S套式引物与psbA引物,以栽培甜荞为材料,进行染色体原位PCR、原位套式PCR与多次原位PCR试验。[结果]高温干燥可以起到与包埋类似的作用;染色体的原位套式PCR效果比原位PCR明显,多次原位PCR次数为5~6效果较佳。16S引物和4.5S引物均显示了4对信号,但位置不同;而psbA引物是单拷贝的,仅显示出1对信号。根据这些信号的位置差异可以区分普通荞麦的5对染色体。[结论]所使用的荞麦染色体原位PCR技术简单易行。 展开更多
关键词 栽培甜荞 IS-PCR 16S RDNA 4.5S RDNA psbA.
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The In Situ PCR Technology on Chromosome of Common Buckwheat
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作者 李分龙 陈庆富 《Agricultural Science & Technology》 CAS 2011年第4期493-496,545,共5页
[Objective] The paper aimed to explore a simple in situ PCR technology for buckwheat.[Method] By using 16S and 4.5S nested primers and psbA primer,the in situ PCR,nested in situ PCR,and multiple in situ PCR were carri... [Objective] The paper aimed to explore a simple in situ PCR technology for buckwheat.[Method] By using 16S and 4.5S nested primers and psbA primer,the in situ PCR,nested in situ PCR,and multiple in situ PCR were carried out on common buckwheat,respectively.[Result] High-temperature drying treatment had the effects similar to that of embedding method.The effect of the nested in situ PCR is better than conventional in situ PCR.A better result could be obtained till the multiple in situ PCR was performed as many as 5-6 times.Four pair of signals could be obtained by using both 16S and 4.5S primers,but their sites differed from each other;psbA primer as a single copy only showed a pair of signals.A total of five pairs of common buckwheat chromosome could be identified according to the difference of the signal's location.[Conclusion] The chromosome in situ PCR technique for buckwheat was simple and feasible. 展开更多
关键词 Fagopyrum esculentum IS-PCR 16S rDNA 4.5S rDNA PSBA
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