Nazaimoon W, Ng M L, Bak K
Department of Biochemistry, Faculty of Medicine, National University of Malaysia, Kuala Lumpur.
Malays J Pathol. 1993 Jun;15(1):75-83.
A simple, non-isotopic in-house enzyme-linked immunoabsorbant assay (ELISA) for human growth hormone (GH) was developed. The assay involved using in-house polyclonal anti-GH adsorbed onto 96-well microtitre plates, commercially prepared mouse monoclonal anti-GH, and goat anti-mouse IgG horseradish peroxidase detection system. Results of recovery and parallelism studies ranged from 95%-106% and 98%-101% respectively, of the expected values. The detection limit of the assay was 0.008 mIU/well or the equivalent to 0.4 mIU/L of undiluted serum. Intra- and interassay coefficients of variations were 4.8%-7.9% and 6.5%-8.7% respectively. Serum GH levels measured in this assay correlated well with those measured in established in-house radioimmunoassays (r = 0.985, p < 0.001) and immunoradiometric assay from NETRIA (r = 0.984, p < 0.001).
开发了一种简单的、非同位素的内部酶联免疫吸附测定法(ELISA)用于检测人生长激素(GH)。该测定法包括使用吸附在96孔微量滴定板上的内部多克隆抗GH、商业制备的小鼠单克隆抗GH以及山羊抗小鼠IgG辣根过氧化物酶检测系统。回收率和平行性研究结果分别为预期值的95%-106%和98%-101%。该测定法的检测限为0.008 mIU/孔,相当于未稀释血清中的0.4 mIU/L。批内和批间变异系数分别为4.8%-7.9%和6.5%-8.7%。用该测定法测得的血清GH水平与既定的内部放射免疫测定法(r = 0.985,p < 0.001)以及NETRIA的免疫放射测定法(r = 0.984,p < 0.001)测得的结果高度相关。