Schössler W, Hiepe F, Montag T, Schmidt H E
Biomed Biochim Acta. 1985;44(7-8):1247-53.
This article describes a solid-phase enzyme immunoassay for the quantitative determination of circulating immune complexes based on the covalent binding of proteins to glass. A quantitative comparison between adsorption to polystyrene and covalent binding to glass gave a protein higher concentration on the glass support. This leads, in connection with the strong attachment of the protein, to a higher sensitivity and precision in immunoassay. The binding of C1q to glass as solid phase offers the possibility to reuse the protein as well as the glass support after accomplishment of the immunoassay which can reduce the cost of the assay in routine work dramatically. Furthermore, the immobilization of C1q to glass gives an extreme stability of the protein which means that the c1q-coated glass supports can be used up to one year under routine conditions.
本文介绍了一种基于蛋白质与玻璃的共价结合来定量测定循环免疫复合物的固相酶免疫测定法。对聚苯乙烯吸附和与玻璃共价结合进行定量比较后发现,玻璃载体上的蛋白质浓度更高。这与蛋白质的牢固附着相结合,使得免疫测定具有更高的灵敏度和精密度。将C1q作为固相结合到玻璃上,使得在免疫测定完成后蛋白质和玻璃载体都有可能重复使用,这可以显著降低常规工作中测定的成本。此外,C1q固定在玻璃上使蛋白质具有极高的稳定性,这意味着在常规条件下,包被有C1q的玻璃载体可使用长达一年。