Buehler J, Macher B A
Anal Biochem. 1986 Nov 1;158(2):283-7. doi: 10.1016/0003-2697(86)90551-8.
Glycosphingolipids carrying carbohydrate sequences recognized by antibodies and lectins can be detected on thin layer chromatograms using an avidin-biotin enzyme system (ABC reagents). This same method can be used to detect glycosphingolipids blot-transferred from thin layer chromatograms to nitrocellulose. This method has certain advantages over the original radioimmunoassay method, including development of positive bands in minutes after incubation with the substrate, avoidance of handling hazardous radioactive materials and stability of reagents. We have demonstrated the usefulness of this method for immunostaining glycosphingolipids with both monoclonal and polyclonal anti-carbohydrate antibodies. These reagents have previously been used to detect carbohydrate antigens in tissues and isolated cells and now it is possible to use the same reagents for the detection of glycosphingolipid antigens on chromatograms.
携带可被抗体和凝集素识别的碳水化合物序列的糖鞘脂,可使用抗生物素蛋白-生物素酶系统(ABC试剂)在薄层色谱图上进行检测。同样的方法可用于检测从薄层色谱图印迹转移至硝酸纤维素膜上的糖鞘脂。与最初的放射免疫测定法相比,该方法具有某些优势,包括与底物孵育后数分钟内即可显现阳性条带、无需处理危险的放射性材料以及试剂稳定性好。我们已经证明了该方法对于用单克隆和多克隆抗碳水化合物抗体免疫染色糖鞘脂的实用性。这些试剂以前曾用于检测组织和分离细胞中的碳水化合物抗原,现在也可以使用相同的试剂来检测色谱图上的糖鞘脂抗原。