Manthorpe M, Skaper S D, Varon S
Brain Res. 1981 Dec 28;230(1-2):295-306. doi: 10.1016/0006-8993(81)90408-x.
Using nerve growth factor (NGF), anti-NGF sera and dissociated neonatal mouse dorsal root ganglionic neurons we present a microculture assay methodology for (1) the titration of neurotrophic factor (NTF) activity in monolayer culture, (2) the titration of NTF antibodies which 'block' NTF biological activity, (3) the titration of NTF antibodies that bind and remove (sequester) NTF from culture medium and (4) a large-scale, convenient, and rapid screening for NTF biological activity as well as for NTF 'blocking' or 'sequestering' antibodies. These quantitative and qualitative in vitro microimmunoassays should be applicable to any neuronotrophic factor or its antibody, even when the agent is only available in crude, unpurified form. Since the microculture systems permit the simultaneous screening of one thousand samples per day they should be useful for the detection and quantitation of monoclonal antibodies present in hybridoma-conditioned media.
利用神经生长因子(NGF)、抗NGF血清和新生小鼠背根神经节解离神经元,我们提出了一种微培养检测方法,用于:(1)单层培养中神经营养因子(NTF)活性的滴定;(2)“阻断”NTF生物活性的NTF抗体的滴定;(3)从培养基中结合并去除(隔离)NTF的NTF抗体的滴定;以及(4)大规模、方便、快速地筛选NTF生物活性以及NTF“阻断”或“隔离”抗体。这些定量和定性的体外微免疫测定法应适用于任何神经营养因子或其抗体,即使该试剂仅以粗制、未纯化的形式存在。由于微培养系统允许每天同时筛选一千个样品,它们应有助于检测和定量杂交瘤条件培养基中存在的单克隆抗体。