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利用高荧光且稳定的半导体量子点对红细胞抗原进行研究。

Investigation of red blood cell antigens with highly fluorescent and stable semiconductor quantum dots.

作者信息

de Farias Patrícia Maria Albuquerque, Santos Beate Saegesser, de Menezes Frederico Duarte, de Carvalho Ferreira Ricardo, Barjas-Castro Maria Lourdes, Castro Vagner, Lima Paulo Roberto Moura, Fontes Adriana, Cesar Carlos Lenz

机构信息

Biofosica e Radiobiologia, Federal University of Pernambuco, Recife, Pernambuco, Brazil.

出版信息

J Biomed Opt. 2005 Jul-Aug;10(4):44023. doi: 10.1117/1.1993257.

Abstract

We report a new methodology for red blood cell antigen expression determination by a simple labeling procedure employing luminescent semiconductor quantum dots. Highly luminescent and stable core shell cadmium sulfide/cadmium hydroxide colloidal particles are obtained, with a predominant size of 9 nm. The core-shell quantum dots are functionalized with glutaraldehyde and conjugated to a monoclonal anti-A antibody to target antigen-A in red blood cell membranes. Erythrocyte samples of blood groups A+, A2+, and O+ are used for this purpose. Confocal microscopy images show that after 30 min of conjugation time, type A+ and A2+ erythrocytes present bright emission, whereas the O+ group cells show no emission. Fluorescence intensity maps show different antigen expressions for the distinct erythrocyte types. The results obtained strongly suggest that this simple labeling procedure may be employed as an efficient tool to investigate quantitatively the distribution and expression of antigens in red blood cell membranes.

摘要

我们报告了一种通过采用发光半导体量子点的简单标记程序来测定红细胞抗原表达的新方法。获得了高发光且稳定的核壳硫化镉/氢氧化镉胶体颗粒,其主要尺寸为9纳米。核壳量子点用戊二醛功能化,并与单克隆抗A抗体偶联,以靶向红细胞膜中的抗原A。为此使用了A+、A2+和O+血型的红细胞样本。共聚焦显微镜图像显示,在结合30分钟后,A+型和A2+型红细胞呈现明亮的发射,而O+型细胞则无发射。荧光强度图显示了不同红细胞类型的不同抗原表达。所获得的结果有力地表明,这种简单的标记程序可用作定量研究红细胞膜中抗原分布和表达的有效工具。

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