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GLYCAN ANALYSIS METHOD, GLYCAN ANALYSIS SYSTEM, PROGRAM FOR GLYCAN ANALYSIS, AND KIT FOR GLYCAN ANALYSIS

机译:糖分析方法,糖分析系统,糖分析程序和糖分析试剂盒

摘要

A sample, which is a mixture of glycans, is fluorescently labeled (S2). The sample is subsequently separated by microchip electrophoresis under a buffer solution with no lectin added as well as under multiple kinds of buffer solutions with different lectins respectively added, and the separated components are fluorescently detected (S3). A high-concentration gel which can produce a molecular-sieving effect is used as the buffer solution. Multiple electropherograms are created from the detection results (S4). A glycan having a lectin specifically attached is delayed during its migration in the buffer solution, so that a peak corresponding to this glycan will effectively disappear. Accordingly, based on the kinds of lectins and the presence/absence of a peak on each of the electropherograms, the structure of each glycan in the sample is estimated and the glycan is identified (S5).
机译:样品是聚糖的混合物,被荧光标记(S 2 )。随后,在未添加凝集素的缓冲液中以及分别添加了不同凝集素的多种缓冲液中,通过微芯片电泳分离样品,并对分离出的成分进行荧光检测(S 3 )。可以产生分子筛作用的高浓度凝胶用作缓冲溶液。根据检测结果(S 4 )创建多个电泳图。具有特异性连接的凝集素的聚糖在其在缓冲溶液中的迁移过程中被延迟,从而对应于该聚糖的峰将有效地消失。因此,根据凝集素的种类和各电泳图中的峰的有无,推定样品中的各聚糖的结构,确定了聚糖(S 5 )。

著录项

  • 公开/公告号US2019265246A1

    专利类型

  • 公开/公告日2019-08-29

    原文格式PDF

  • 申请/专利权人 SHIMADZU CORPORATION;

    申请/专利号US201916286937

  • 发明设计人 MITSUHIRO KINOSHITA;

    申请日2019-02-27

  • 分类号G01N33/58;G01N27/447;G16C20/20;

  • 国家 US

  • 入库时间 2022-08-21 12:07:30

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