Iijima S, Shiba K, Inoue J, Yoshida T, Kimura M
Toxicology Laboratory, Kyoritsu College of Pharmacy, Tokyo, Japan.
J Clin Lab Anal. 1997;11(4):220-4. doi: 10.1002/(sici)1098-2825(1997)11:4<220::aid-jcla8>3.0.co;2-c.
A systematic detection method for the single performance of cellulose acetate (CA) membrane isoelectric focusing to detect six different types of information on protein abnormalities was developed. High-voltage isoelectric focusing was carried out on six layers of CA membrane using a thermoelectric cooling apparatus. After electrophoresis, the proteins on the top, the third, the fourth, the fifth, and the bottom CA membrane were transferred to a polyvinylidene difluoride (PVDF) membrane by a simple contact printing procedure to detect IgM, kappa-chain, lambda-chain, IgA, and IgG, respectively. Each PVDF membrane revealed the microheterogeneity of these immunoglobulins using specified anti-serum and enzyme immunostaining. The second CA membrane was stained with Coomassie brilliant blue G250 to detect serum protein patterns. All stained membranes showed clear electrophoretic patterns of immunoglobulin microheterogeneity. By our method, immunoglobulin abnormalities in serum could be screened out using six different types of information obtained simultaneously.
开发了一种用于醋酸纤维素(CA)膜等电聚焦单次性能的系统检测方法,以检测六种不同类型的蛋白质异常信息。使用热电冷却装置在六层CA膜上进行高压等电聚焦。电泳后,通过简单的接触印迹程序将顶部、第三、第四、第五和底部CA膜上的蛋白质转移到聚偏二氟乙烯(PVDF)膜上,分别检测IgM、κ链、λ链、IgA和IgG。每张PVDF膜使用特定的抗血清和酶免疫染色显示这些免疫球蛋白的微异质性。第二张CA膜用考马斯亮蓝G250染色以检测血清蛋白模式。所有染色的膜均显示出免疫球蛋白微异质性的清晰电泳图谱。通过我们的方法,可以利用同时获得的六种不同类型的信息筛选出血清中的免疫球蛋白异常。