Azwai S M, Carter S D, Woldehiwet Z
Department of Veterinary Pathology, University of Liverpool, U.K.
J Comp Pathol. 1993 Aug;109(2):187-95. doi: 10.1016/s0021-9975(08)80262-9.
Immunoglobulins G and M were prepared from camel sera by ammonium sulphate precipitation, gel filtration and fast protein liquid chromatography (ion exchange). Heavy and light chains were identified by polyacrylamide gel electrophoresis and Western blotting. IgG subclasses were isolated by DEAE ion exchange chromatography and shown to have different electrophoretic motilities. No molecules corresponding to IgA were detected. Rabbit anti-serum against camel IgG was generated and its specificity shown by Western blotting.
通过硫酸铵沉淀、凝胶过滤和快速蛋白质液相色谱法(离子交换)从骆驼血清中制备免疫球蛋白G和M。通过聚丙烯酰胺凝胶电泳和蛋白质印迹法鉴定重链和轻链。通过DEAE离子交换色谱法分离IgG亚类,并显示其具有不同的电泳迁移率。未检测到对应于IgA的分子。制备了兔抗骆驼IgG血清,并通过蛋白质印迹法显示其特异性。