摘要
用辣根过氧化物酶标记羊抗人apoAIIgG, 建立了检测兔肝细胞膜HDL受体的酶联免疫吸附检测法. 测定时,HDL结合量按抗体配体抗配体抗体酶交联物反应制作的标准曲线确定; 膜蛋白非特异吸附则用与酶交联的抗体来源相同的同种动物血浆HDL平行抑制试验消除. 实验测得正常家兔肝细胞膜HDL受体Kd 值为717 ±118 mg/L, Bmax值为(6225±1461) mg/g (n= 7).
Using HRP conjugated goat anti human apoAI IgG, an enzyme linked immunosorbent receptor assay was developed for measurement of high density lipoprotein (HDL) receptors on rabbit liver plasma membranes. A curve of anti apoAI IgG binding to known amounts of HDL was constructed to quantify the HDL bound. Parallel samples with 25 fold excess goat plasma HDL were assayed to detect nonspecific binding . The results showed that the K d and B max of rabbit liver plasma membrane HDL receptors were (7 17±1 18)mg/L and (622 5± 146 1)mg/L respectively ( n =7).
出处
《生物化学与生物物理进展》
SCIE
CAS
CSCD
北大核心
1999年第5期461-464,共4页
Progress In Biochemistry and Biophysics
基金
国家教委博士学科点专项科研基金
关键词
受体
肝细胞膜
高密度脂蛋白
ELISA
HDL receptor, liver plasma membrane, enzyme linked immunosorbent receptor assay