Nicholson L V, Davison K, Falkous G, Harwood C, O'Donnell E, Slater C R, Harris J B
Muscular Dystrophy Group Research Laboratory, Newcastle General Hospital, Newcastle upon Tyne, U.K.
J Neurol Sci. 1989 Dec;94(1-3):125-36. doi: 10.1016/0022-510x(89)90223-2.
The value of analysing dystrophin on Western blots of skeletal muscle for the differential diagnosis of Xp21 muscular dystrophies is now fairly well established. Here we describe a sensitive system based on monoclonal antibodies to dystrophin. The specificity of the antibodies was established and experiments were undertaken to identify the source of dystrophin-related protein bands which were detected on blots of normal skeletal muscle. These investigations formed a necessary preliminary study to the application of the assay to samples of muscle obtained at biopsy from patients with Duchenne and Becker muscular dystrophy.
通过骨骼肌的蛋白质免疫印迹法分析抗肌萎缩蛋白以鉴别Xp21型肌营养不良症的价值现已得到充分证实。在此,我们描述了一种基于抗肌萎缩蛋白单克隆抗体的灵敏检测系统。确定了抗体的特异性,并开展实验以鉴定在正常骨骼肌印迹上检测到的抗肌萎缩蛋白相关蛋白条带的来源。这些研究是将该检测方法应用于杜兴氏和贝克氏肌营养不良症患者活检获得的肌肉样本的必要前期研究。