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High-throughput quantitative detection of triple-negative breast cancer-associated expressed miRNAs by rolling circle amplification on fluorescence-encoded microspheres 被引量:1
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作者 Jieyu Liu Liming Zhang +3 位作者 Wentao Zeng Lihua Zhang Nongyue He Zhuoxuan Lu 《Chinese Chemical Letters》 SCIE CAS CSCD 2023年第9期199-203,共5页
Compared with other types of breast cancer,triple-negative breast cancer(TNBC)has the characteristics of a high degree of malignancy and poor prognosis.Early diagnosis of TNBC through biological markers and timely dev... Compared with other types of breast cancer,triple-negative breast cancer(TNBC)has the characteristics of a high degree of malignancy and poor prognosis.Early diagnosis of TNBC through biological markers and timely development of effective treatment methods can reduce its mortality.Many Research experiments have confirmed that some specific mi RNA expression profiles in TNBC can used as markers for early diagnosis.However,detecting the expression profiles of multiple groups of miRNAs according to traditional detection methods is complicated and consumes many samples.To address this issue,we developed a method for high-throughput,high-sensitivity quantitative detection of multiple sets of miRNAs(including mi R-16,mi R-21,mi R-92,mi R-199,and mi R-342)specifically expressed in TNBC by rolling circle amplification(RCA)on fluorescence-encoded microspheres.Through the optimization of reaction system conditions,the developed method showed an extensive linear dynamic range and high sensitivity for all five miRNAs with the lowest limit of detection of 2 fmol/L.Meanwhile,this high-throughput detection method also appeared reasonable specificity.Only in the presence of a specific target miRNA,the fluorescence signal on the correspondingly encoded microspheres is significantly increased,while the fluorescence signal on other non-correspondingly encoded microspheres is almost negligible.Furthermore,this process exhibited good recovery and reproducibility in serum.The advantages of this method allow us to more conveniently obtain the expression profiles of multiple groups of TNBC-associated mi RNAs,which is beneficial for the early detection of TNBC. 展开更多
关键词 MICRORNAS Rolling circle amplification fluorescence-encoded microspheres HIGH-THROUGHPUT Triple-negative breast cancer
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Synthesis and adsorption performance of lead ion-imprinted micro-beads with combination of two functional monomers 被引量:9
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作者 Linyan Zhu Zhiliang Zhu +2 位作者 Ronghua Zhang Jun Hong Yanling Qiu 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2011年第12期1955-1961,共7页
A novel ion-imprinted polymer, lead ion-imprinted micro-beads with combination of two functional monomers, was synthesized using the W/O/W polymerization method. Two functional monomers, 1,12-dodecanediol-O,O’-diphen... A novel ion-imprinted polymer, lead ion-imprinted micro-beads with combination of two functional monomers, was synthesized using the W/O/W polymerization method. Two functional monomers, 1,12-dodecanediol-O,O’-diphenyl-phosphonic acid (DDDPA) and 4-vinylpyridine, were used to form a suitable construction with micro-pores fitting the template and recognition sites. The eflects of adsorbent dosage, solution pH and the competitive ions on the adsorption and separation eflciency of lead ions were investigated. The lead ion-imprinted micro-beads were eflcient for lead ions removal from aqueous solution in a broad pH range (4–9), when the adsorbent dosage was above 0.1 g/L. The adsorption process obeyed the pseudo second-order kinetics model and it only took half an hour to reach the equilibrium. The adsorption isotherm of lead ion was described by the Langmuir model (R2 0.99) with a maximum adsorption capacity of 116.9 mg/g. In the presence of competitive ions Co2+ and Cd2+, the lead ion-imprinted micro-beads showed a high selectivity for lead ions. The selectivity coeficient of Pb2+/Cd2+ and Pb2+/Co2+are 99.3 and 114.7, respectively. 展开更多
关键词 lead ions ADSORPTION lead ion-imprinted micro-beads selective separation RECOGNITION
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一种高效的功能基因分离解析法
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作者 袁晓东 李国印 汤敏谦 《遗传》 CAS CSCD 北大核心 2002年第3期320-324,共5页
人类基因组计划 (HumanGenomeProject)的实施揭开了各种生物基因组解析的序幕[1~ 3 ] 。随着各种生物的基因组解析的顺利进行 ,遗传基因的功能研究以及寻找新的功能基因变得越来越重要。本文介绍的Mega cloneTM技术、MegasortTM技术[4... 人类基因组计划 (HumanGenomeProject)的实施揭开了各种生物基因组解析的序幕[1~ 3 ] 。随着各种生物的基因组解析的顺利进行 ,遗传基因的功能研究以及寻找新的功能基因变得越来越重要。本文介绍的Mega cloneTM技术、MegasortTM技术[4 ] 以及MPSS 技术[5] 可以高效地分离解析各种功能基因。 展开更多
关键词 功能基因 分离解析法 Megaclone^TM Megasort^TM MPSS micro-beads
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