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[AS-PCR amplification in identification of Sedum sarmentosum with its relative species].

Authors: Dong-mei, Xie; Lu-qi, Huang; Min-jian, Qin; De-qun, Wang; Chao, Jiang; Yuan, Yuan;

[AS-PCR amplification in identification of Sedum sarmentosum with its relative species].

Abstract

To develop a scientific and effective method for identification of Sedum sarmentosum and its relative materials easily confused.DNA templates were extracted from plants, and DNA fragments of cpDNA trnL (tRNA-Leu) gene and trnL-trnF intergenic spacer were amplified and sequenced subsequently. trnL-trnF sequences of all samples were aligned.The allele specific PCR method was studied with the designed allele-specific for distinguishing different samples. The result indicated that 300 bp and 500 bp DNA fragments were amplified from Sedum sarmentosum, where no any fragment was amplified from its relative species under the same reaction condition.The primers designed in this study are specific for Sedum sarmentosum from its relative species.

Keywords

DNA, Chloroplast, Sequence Analysis, DNA, Polymerase Chain Reaction, Alleles, Sedum, DNA Primers

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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Average
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