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细胞追踪测速法作为一种确定磁共轭抗体饱和结合的工具。

Cell tracking velocimetry as a tool for defining saturation binding of magnetically conjugated antibodies.

作者信息

Leigh Diane R, Steinert Steffen, Moore Lee R, Chalmers Jeffrey J, Zborowski Maciej

机构信息

Department of Biomedical Engineering, The Cleveland Clinic Foundation, Cleveland, OH 44195, USA.

出版信息

Cytometry A. 2005 Aug;66(2):103-8. doi: 10.1002/cyto.a.20155.

Abstract

BACKGROUND

Continuous flow immunomagnetic separation is an attractive alternative to current batch mode immunomagnetic separation methods because it is capable of high sorting speeds at mild cell conditions, and grants the operator better control of separation process. The control of the separation is dependent on knowledge of the amount of magnetic label attached to the cell (magnetic labeling intensity), however. Determination of the magnetic labeling is accomplished by measuring cell magnetophoretic mobility using a newly developed technique of Cell Tracking Velocimetry (CTV).

METHODS

Flow cytometry was used to define the antibody binding characteristics of a fluorescently tagged primary antibody. Subsequently, CTV was used to measure antibody-binding characteristics of a magnetically tagged secondary antibody.

RESULTS

The results of this study show that CTV is capable of providing valuable information concerning the cell labeling by magnetically tagged antibodies. It was demonstrated that the magnetically conjugated antibody binding curve exhibits the same exponential increase to saturation characteristics as that seen with the fluorescently tagged antibody. Further, it was shown that the intensity of the secondary magnetic labeling is directly proportional to the intensity of the primary fluorescent label.

CONCLUSIONS

CTV is an accurate tool for evaluation of magnetically conjugated antibodies. The ability to determine the intensity of magnetic labeling is necessary for the development of continuous flow immunomagnetic separations based on cell magnetophoresis.

摘要

背景

连续流免疫磁分离是当前批量模式免疫磁分离方法的一种有吸引力的替代方法,因为它能够在温和的细胞条件下实现高分选速度,并使操作人员能更好地控制分离过程。然而,分离的控制取决于对附着在细胞上的磁性标记量(磁性标记强度)的了解。磁性标记的测定是通过使用新开发的细胞跟踪测速技术(CTV)测量细胞磁泳迁移率来完成的。

方法

使用流式细胞术来确定荧光标记的一抗的抗体结合特性。随后,使用CTV来测量磁性标记的二抗的抗体结合特性。

结果

本研究结果表明,CTV能够提供有关磁性标记抗体对细胞标记的有价值信息。结果表明,磁性偶联抗体结合曲线呈现出与荧光标记抗体相同的指数增长至饱和特性。此外,还表明二抗磁性标记的强度与一抗荧光标记的强度成正比。

结论

CTV是评估磁性偶联抗体的准确工具。确定磁性标记强度的能力对于基于细胞磁泳作用的连续流免疫磁分离的发展是必要的。

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