A Homogeneous Chemiluminescent Immunoassay Method

被引:67
作者
Akhavan-Tafti, Hashem [1 ]
Binger, Dean G. [2 ]
Blackwood, John J. [2 ]
Chen, Ying [2 ]
Creager, Richard S. [2 ]
de Silva, Renuka [1 ]
Eickholt, Robert A. [1 ]
Gaibor, Jose E. [2 ]
Handley, Richard S. [1 ]
Kapsner, Kenneth P. [2 ]
Lopac, Senja K. [2 ]
Mazelis, Michael E. [1 ]
McLernon, Terri L. [2 ]
Mendoza, James D. [2 ]
Odegaard, Bruce H. [2 ]
Reddy, Sarada G. [1 ]
Salvati, Michael [2 ]
Schoenfelner, Barry A. [1 ]
Shapir, Nir [2 ]
Shelly, Katherine R. [2 ]
Todtleben, Jeff C. [2 ]
Wang, Guoping [1 ]
Xie, Wenhua [1 ]
机构
[1] Beckman Coulter Inc, Southfield, MI 48033 USA
[2] Beckman Coulter Inc, Chaska, MN 55318 USA
关键词
ENZYME FRAGMENT COMPLEMENTATION; FLUORESCENCE POLARIZATION ASSAYS; LINKED-IMMUNOSORBENT-ASSAY; HIGH-THROUGHPUT; BINDING-KINETICS; KINASE;
D O I
10.1021/ja312039k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new homogeneous chemiluminescent immunoassay method featuring the use of specific binding members separately labeled with an acridan-based chemiluminescent compound and a peroxidase is reported. Formation of an immunocomplex brings the chemiluminescent compound and the peroxidase into close proximity. Without any separation steps, a chemiluminescent signal is generated upon addition of a trigger solution, and the intensity is directly correlated to the quantity of the analyte.
引用
收藏
页码:4191 / 4194
页数:4
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