Aubert D, Lepan H, Lemaire P, Foudrinier F, Marx-Chemla C, Bonhomme A, Pinon J M
Laboratoire de Parasitologie-Mycologie, C. H. U., Reims, France.
Electrophoresis. 1995 Mar;16(3):354-56. doi: 10.1002/elps.1150160160.
We report the use of enzyme-linked immunofiltration-assay (ELIFA) for rapid detection of Toxoplasma gondii DNA after transfer to nitrocellulose or nylon membranes. Saturation, specific labeling with a nonradioactive oligonucleotide probe and washing steps are included in an active filtration process, which is controled by microcomputer regulating reagent flow. This method provides excellent specificity, reproducibility and repeatability. Recycling in a closed circuit or by reversing the direction of flow provides the advantage of reducing the required volume of costly reagents (e.g. probes). ELIFA does not require lengthy membrane manipulation, and hybridization as well as stringency and revelation steps can be automated. The procedure can be carried out in less than 2 h, which is a major time saving compared to conventional solid-phase molecular hybridization techniques.
我们报告了酶联免疫过滤测定法(ELIFA)在将弓形虫DNA转移至硝酸纤维素或尼龙膜后用于快速检测的情况。活性过滤过程包括饱和、用非放射性寡核苷酸探针进行特异性标记以及洗涤步骤,该过程由微型计算机调节试剂流动来控制。此方法具有出色的特异性、重现性和可重复性。通过在封闭回路中循环或反向流动可减少昂贵试剂(如探针)的所需用量。ELIFA不需要长时间的膜操作,杂交以及严格性和显影步骤均可实现自动化。该程序可在不到2小时内完成,与传统的固相分子杂交技术相比,这大大节省了时间。