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1)  Single cell nested RT-PCR
单细胞巢式RT-PCR
2)  single-cell RT-PCR
单细胞RT-PCR
1.
Methods: Human neutrophils were isolated and purified from volunteers,total RNA was extracted and a regular RT-PCR aiming at IL-8Rβ mRNA was performed to ascertain its expression profile in human neutrophils and optimize the reaction conditions for the following single-cell RT-PCR procedures.
方法:采用倍比稀释相对定量单细胞RT-PCR方法分离纯化人外周血中性粒细胞并提取总RNA,针对IL-8RβmRNA设计引物,进行RT-PCR确认IL-8Rβ在中性粒细胞中的基因表达并优化反应条件。
3)  preimplantation genetic diagnosis (PGD)
单细胞巢式PCR
4)  Nested RT-PCR
巢式RT-PCR
1.
Development of nested RT-PCR for detection animal rabies virus
动物狂犬病病毒巢式RT-PCR检测方法的建立
2.
To study the incidence, the types of fusion genes and the clinical significance of rearrangements of mixed lineage leukemia (MLL) gene in acute leukemia (AL), the rearrangements of MLL gene of 60 patients with AL were detected by fluorescence in situ hybridization (FISH) and 6 types of common fusion genes resulting from the rearrangements of MLL gene were detected by nested RT-PCR.
为了研究混合系白血病(MLL)基因重排在急性白血病(AL)中的发生率、融合基因类型及其临床意义,用荧光原位杂交技术检测60例急性白血病(AL)患者MLL基因重排,对于MLL基因重排阳性的患者,用巢式RT-PCR方法检测MLL基因重排形成的6种常见融合基因类型。
3.
Methods CK19mRNA expression was detected by nested RT-PCR in the peripheral blood from 60 lung cancer patients.
方法以CK-19为标记,采用巢式RT-PCR和半定量方法对肺癌患者外周血中微转移灶的检测,比较治疗前后外周血中癌细胞数的相对变化。
5)  semi-nested RT-PCR
半巢式RT-PCR
1.
Detection of respiratory syncytial virus by semi-nested RT-PCR;
半巢式RT-PCR法检测呼吸道合胞病毒
2.
Detection of Tobacco ringspot virus and Tomato ringspot virus by semi-nested RT-PCR;
烟草环斑病毒和番茄环斑病毒的半巢式RT-PCR检测
3.
Detection of Bean pod mottle virus by semi-nested RT-PCR in imported soybean;
半巢式RT-PCR检测进口大豆中菜豆荚斑驳病毒的研究
6)  RT-seminested PCR
RT-半巢式PCR
1.
Reverse transcription polymerase chain reaction(RT-PCR),RT-seminested PCR and reverse transcription loop-mediated isothermal amplification(RT-LAMP) assays were compared to detect norovirus in oysters.
采用RT-PCR、RT-半巢式PCR(seminested PCR)和RT-环介导等温扩增(LAMP)三种分子生物学方法分别检测了牡蛎中经粪便污染的诺如病毒。
补充资料:单细胞克隆技术
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性质:平板培养是为了分离和获得单细胞无性系并对不同的无性系进行研究,揭示它们在生理、生化和遗传上的差异而设计的一种单细胞培养技术,也称单细胞克隆技术。由于它具有筛选效率高、筛选量大、操作简单便等优点,因而被广泛地用于遗传变异、细胞分裂分化、细胞次生代谢物合成等项研究。这项技术是1960年Bergmann首创的,操作时将单细胞悬浮液与30~35℃呈融化状态的琼脂均匀混合,然后注入培养皿中成一薄层,琼脂冷却固化后,均匀分布的细胞就在其中成长,由于薄薄的一层固化琼脂呈平板状,故称它为平板培养。

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