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Efficiency of improved RAPD and ISSR markers in assessing genetic diversity and relationships in Angelica sinensis (Oliv.) Diels varieties of China Electron. J. Biotechnol.
Mei,Zhiqiang; Zhang,Chun; Khan,Asaduzzaman; Zhu,Ye; Tania,Mousumi; Luo,Peiyi; Fu,Junjiang.
Background Angelica sinensis is a well-known traditional Chinese medicinal plant. We aimed to assess the genetic diversity and relationships in A. sinensis cultivars collected from different locations of China and also some other Angelica species. Results We employed an improved random amplified polymorphic DNA (RAPD) technique for the amplification of DNA materials from ten Angelica cultivars, and the results were verified by inter-simple sequence repeat (ISSR) analysis. Twenty six RAPD primers were used for RAPD, and the amplified bands were found highly polymorphic (96%). Each primer amplified 8-14 bands with an average of 10.25. The cluster dendrogram showed that the similarity coefficients ranged from 0.41 to 0.92. The similarity coefficients were...
Tipo: Journal article Palavras-chave: Angelica sinensis; Genetic authentication; Inter-simple sequence repeat; Random amplified polymorphic DNA; Substitutes.
Ano: 2015 URL: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582015000200006
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Establishment of a HEK293T cell line able to site-specifically integrate and stably express GDNF by rAAV-2 vector Electron. J. Biotechnol.
Zhang,Jinju; Zhang,Yun; Liu,Xiaomei; Xiang,Jingjing; Zhang,Chun.
Background: Using recombinant adeno-associated virus 2 (rAAV-2), we attempted to establish a HEK293T cell line that is able to site-specifically integrate and stably express glial cell line-derived neurotrophic factor (GDNF). Results:Recombinant vector with enhanced green fluorescent protein (EGFP) and GDNF (pTR-P5-EGFP-IRES-GDNF), as well as that carrying Rep genes and SV40 promoters (pSVAV2) were constructed and packed. HEK293T cells were co-infected with rAAV-2/EGFP-GDNF and rAAV-2/SVAV2 virus separately at 1 x 10(4),1 x 10(5),and 1x10(6) of multiplicity of infection (MOI). The efficiency of transduction was detected using flow cytometry. Additionally, the infected HEK293T cells were separately validated by touchdown polymerase chain reaction (PCR) and...
Tipo: Journal article Palavras-chave: Glial cell line-derived neurotrophic factor; Multiplicity of infection; Recombinant adeno-associated virus 2; Site-specific integration; Transduction.
Ano: 2016 URL: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582016000400011
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