Melrose J, Ghosh P, Jacoby A
Raymond Purves Bone and Joint Research Laboratories, University of Sydney at the Royal North Shore Hospital of Sydney, St. Leonards, N.S.W., Australia.
Clin Chim Acta. 1994 Feb;225(1):17-28. doi: 10.1016/0009-8981(94)90024-8.
A solid phase enzyme linked immunosorbent filtration assay (ELIFA) has been developed for secretory leucocyte proteinase inhibitor (SLPI) utilising polyclonal anti-recombinant SLPI (anti-rSLPI) and polyclonal anti-bronchial mucus proteinase inhibitor (anti-BLPI) IgG samples. Millipore HATF nitrocellulose 96-well plates were used as receptacles for the assay and a commercial goat anti-rabbit IgG alkaline phosphatase conjugate was used as a secondary antibody for quantitation of levels of primary antibodies bound to rSLPI in the plate wells. Antigen bound to the HATF plates efficiently and the washing/blocking steps were simplified by vacuum filtration of samples resulting in a rapid and convenient assay system. The ELIFA was also sensitive and a detection limit of 0.1 ng SLPI/well was achieved using either anti-SLPI or anti-BLPI as primary antibodies. This assay was used to demonstrate the production of SLPI at moderate levels (0.5-3 ng/ml media) by human articular chondrocytes grown in monolayer culture.
利用多克隆抗重组分泌性白细胞蛋白酶抑制剂(anti-rSLPI)和多克隆抗支气管黏液蛋白酶抑制剂(anti-BLPI)IgG样本,开发了一种用于检测分泌性白细胞蛋白酶抑制剂(SLPI)的固相酶联免疫吸附过滤测定法(ELIFA)。使用密理博HATF硝酸纤维素96孔板作为测定容器,并使用商业化的山羊抗兔IgG碱性磷酸酶偶联物作为二抗,用于定量板孔中与rSLPI结合的一抗水平。抗原能有效结合到HATF板上,通过对样品进行真空过滤简化了洗涤/封闭步骤,从而形成了一种快速便捷的测定系统。该ELIFA也很灵敏,使用抗SLPI或抗BLPI作为一抗时,检测限可达0.1 ng SLPI/孔。该测定法用于证明单层培养的人关节软骨细胞能以中等水平(0.5 - 3 ng/ml培养基)产生SLPI。