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QR code labeling system for Xueteng-related herbs based on DNA barcode 被引量:4
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作者 Hong Zhou Shuang-jiao Ma +4 位作者 Jing-yuan Song Yu-lin Lin Zheng-jun Wu Zheng-zhou Han Hui Yao 《Chinese Herbal Medicines》 CAS 2019年第1期52-59,共8页
Objective: Xueteng-related herbs include Spatholobi Caulis(Jixueteng in Chinese), Sargentodoxae Caulis(Daxueteng in Chinese), Kadsurae Caulis(Dianjixueteng in Chinese), and other medicinal plant stems that release red... Objective: Xueteng-related herbs include Spatholobi Caulis(Jixueteng in Chinese), Sargentodoxae Caulis(Daxueteng in Chinese), Kadsurae Caulis(Dianjixueteng in Chinese), and other medicinal plant stems that release reddish-brown juices after being cut. However, similarity in phonetic spelling and sound leads to their misuse in clinic or commercial circulation. Accurate labeling is imperative as well as effective for species identification.Methods: In this study, the ITS2 sequences of 76 samples of Xueteng-related herbs were obtained and analyzed to identify them. And then they were converted into QR codes using the open source PHP QR code. Also, a DNA barcode reference library was established according to these sequences and was used to authenticate the 25 samples of Xueteng-related herbs collected from the market.Results: The lengths of the ITS2 sequences of different Xueteng-related herbs ranged from 207 to 235 bp and the GC contents were 57.5%-71.0%. Jixueteng, Daxueteng, and Dianjixueteng were clustered into three clades respectively in the neighbor-joining(NJ) phylogenetic tree, and the efficiency of the BLAST method was 100%. The ITS2 sequences of different Xueteng-related herbs were presented vividly and specifically in QR code. Twenty-two of all 25 commercial samples were consistent with the original labels, whereas three samples marked "Dianjixueteng" were authenticated as "Jixueteng".Conclusion: QR code labeling system based on DNA barcode is an effective labeling system of Xuetengrelated herbs for their circulation regulation. 展开更多
关键词 dna labeling system identification ITS2 QR code Xueteng-related herbs
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Systematic investigation of bioorthogonal cellular DNA metabolic labeling in a photo-controlled manner
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作者 Shaokang Jia Shixi Yang +4 位作者 Huimin Ji Shuang Peng Kun Chen Zhiyong He Xiang Zhou 《Chinese Chemical Letters》 SCIE CAS CSCD 2020年第5期1104-1108,共5页
Bioorthogonal cleavage and ligation reactions together form one more integrated system about the repertoire of bioorthogonal chemistry,capacitating an array of thrilling new biological applications.The bond-cleavage t... Bioorthogonal cleavage and ligation reactions together form one more integrated system about the repertoire of bioorthogonal chemistry,capacitating an array of thrilling new biological applications.The bond-cleavage type and position of biomolecular remain a great challenge,which determines the metabolic pathway of the targets in living systems.Herein we designed two linkages of methylene and carbonyl group attached the N-3 position of the 5-ethynyl-2’-deoxyuridine(EdU)base or the oxygen atom at deoxyribose 3’position to a photocaging group,which would be cleaved by irradiation with 365 nm ultraviolet light.EdU derivatives linked by methylene at the N-3 position had better photodecage efficiency and stability in the absence of light.This paper provides a strategy for studying the nucleoside metabolic pathways in cells,which can easily and conveniently evaluate the effect of the position and type of the linkages.The developed strategy affords a reference for controlling spatial and temporal metabolism of small-molecule drugs,allowing direct manipulation of intact cells under physiological conditions. 展开更多
关键词 dna metabolic labeling Bioorthogonal chemistry Photocage group Modified nucleoside Cell imaging
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DNA labelled graphs with DNA computing 被引量:2
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作者 WANG ShiYing YUAN Jun LIN ShangWei 《Science China Mathematics》 SCIE 2008年第3期437-452,共16页
Let k ? 2, 1 ? i ? k and α ? 1 be three integers. For any multiset which consists of some k-long oligonucleotides, a DNA labelled graph is defined as follows: each oligonucleotide from the multiset becomes a point; t... Let k ? 2, 1 ? i ? k and α ? 1 be three integers. For any multiset which consists of some k-long oligonucleotides, a DNA labelled graph is defined as follows: each oligonucleotide from the multiset becomes a point; two points are connected by an arc from the first point to the second one if the i rightmost nucleotides of the first point overlap with the i leftmost nucleotides of the second one. We say that a directed graph D can be (k, i; α)-labelled if it is possible to assign a label (l 1(x), ..., l k (x)) to each point x of D such that l j (x) ? {0, ..., α ? 1} for any j ? {1, ..., k} and (x, y) ? E(D) if and only if (l k?i+1(x), ..., l k (x)) = (l 1(y), ..., l i (y)). By the biological background, a directed graph is a DNA labelled graph if there exist two integers k, i such that it is (k, i; 4)-labelled. In this paper, a detailed discussion of DNA labelled graphs is given. Firstly, we study the relationship between DNA labelled graphs and some existing directed graph classes. Secondly, it is shown that for any DNA labelled graph, there exists a positive integer i such that it is (2i, i; 4)-labelled. Furthermore, the smallest i is determined, and a polynomial-time algorithm is introduced to give a (2i, i; 4)-labelling for a given DNA labelled graph. Finally, a DNA algorithm is given to find all paths from one given point to another in a (2i, i; 4)-labelled directed graph. 展开更多
关键词 dna labelled graphs dna computing directed line-graphs 05C28
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Evaluation of ECL Labeled DNA Probe for the Diagnosis of Falciparum Malaria
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《Chinese Medical Journal》 SCIE CAS CSCD 1994年第7期66-66,共1页
A commercially available non—radioactive DNA labelling kit "enhanced chemiluminescence"(ECL) was evaluated for the diagnosis of falciparum malaria. The results showed that ECL labeled probe successfully det... A commercially available non—radioactive DNA labelling kit "enhanced chemiluminescence"(ECL) was evaluated for the diagnosis of falciparum malaria. The results showed that ECL labeled probe successfully detected as little as 25 pg. Purified DNA of 0.001% parasitemia of cultured Plasmodium falciparum and did not react with human 展开更多
关键词 dna ECL Evaluation of ECL Labeled dna Probe for the Diagnosis of Falciparum Malaria
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Base pair distance analysis in single DNA molecule by direct stochastic optical reconstruction microscopy
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作者 Suresh Kumar Chakkarapani Guenyoung Park Seong Ho Kang 《Chinese Chemical Letters》 SCIE CAS CSCD 2015年第12期1490-1495,共6页
Precise fluorescence imaging of single l-DNA molecules for base pair distance analysis requires a superresolution technique, as these distances are on the order of diffraction limit. Individual l-DNA molecules interca... Precise fluorescence imaging of single l-DNA molecules for base pair distance analysis requires a superresolution technique, as these distances are on the order of diffraction limit. Individual l-DNA molecules intercalated with the fluorescent dye YOYO-1 were investigated at subdiffraction spatial resolution by direct stochastic optical reconstruction microscopy(d STORM). Various dye-to-DNA base pair ratios were imaged by photoswitching YOYO-1 between the fluorescent state and the dark state using two laser sources. The acquired images were reconstructed into a super-resolution image by applying Gaussian fitting to the centroid of the point spread function. By measuring the distances between localized fluorophores, the base pair distances in single DNA molecules for dye-to-DNA base pair ratios of 1:50,1:100, and 1:500 were calculated to be 17.1 0.8 nm, 34.3 2.2 nm, and 170.3 8.1 nm[17_TD$IF], respectively,which were in agreement with theoretical values. These results demonstrate that intercalating dye in a single DNA molecule can be photoswitched without the use of an activator fluorophore, and that super-localization precision at a spatial resolution of 17 nm was experimentally achieved. 展开更多
关键词 stochastic dna reconstructed fitting applying localization correction frames label localized
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Preparation of Digoxigenin labelled Probe and Detection of HBV DNA in Liver and Extrabepatic Tissue with in Situ Hybridization
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《Chinese Medical Journal》 SCIE CAS CSCD 1994年第10期75-75,共1页
A new rapid technique for intrahepatic and extrahepatic HBV DNA detection by using digoxigenin labelled probe with in situ hybridization was developed.This technique has the advantage of being non-radioactive and a qu... A new rapid technique for intrahepatic and extrahepatic HBV DNA detection by using digoxigenin labelled probe with in situ hybridization was developed.This technique has the advantage of being non-radioactive and a quick procedure yielding stable results and showing a clear background. 展开更多
关键词 HBV dna Preparation of Digoxigenin labelled Probe and Detection of HBV dna in Liver and Extrabepatic Tissue with in Situ Hybridization
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Winning the Wine War:Could DNA Help the Fight to Keep Bottle Labels Honest?
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作者 Emma Marris 何萧蓉 《当代外语研究》 2005年第6期37-38,36,共3页
葡萄酒的魔力在于她成分的复杂性,而正是如此才使得她的品质微妙得难以鉴定。由此在掺假者和鉴定者间展开了一场葡萄酒的“军备竞赛”。专家们使用同位素探测以及套色技术来鉴定葡萄酒的品质,但由于各葡萄产地之间存在着地区差异,这些... 葡萄酒的魔力在于她成分的复杂性,而正是如此才使得她的品质微妙得难以鉴定。由此在掺假者和鉴定者间展开了一场葡萄酒的“军备竞赛”。专家们使用同位素探测以及套色技术来鉴定葡萄酒的品质,但由于各葡萄产地之间存在着地区差异,这些方法并不能一劳永逸。目前,法国蒙比利埃大学的科学家们正设法通过萃取果汁来提取和净化葡萄的DNA成分,从而达到鉴定品质的目的。虽然短时间内他们还不能完成这个计划,但是前景是乐观的。 展开更多
关键词 葡萄酒 Winning the Wine War:Could dna Help the Fight to Keep Bottle Labels Honest dna
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