首页> 外国专利> ELECTROPHORESIS METHOD OPTIMIZED TO GRAIN PROTEIN, GEL FOR ELECTROPHORESIS USED THEREFOR, BUFFER SOLUTION, AND SAMPLE EXTRACT

ELECTROPHORESIS METHOD OPTIMIZED TO GRAIN PROTEIN, GEL FOR ELECTROPHORESIS USED THEREFOR, BUFFER SOLUTION, AND SAMPLE EXTRACT

机译:优化了谷物蛋白的电泳方法,用于电泳的凝胶法,缓冲液和样品提取物

摘要

PROBLEM TO BE SOLVED: To achieve a clear migration pattern in a shorter time than by a conventional method when electrophoresis is performed on grain proteins.;SOLUTION: Eelectrophoresis is performed on the grain protein with three essential elements of (1) a polyacrylamide gel of which the maximum degree of swelling in water is between 1.3-2.0, (2) a sample extract for SDS-PAGE containing of a thiolic reducer which corresponds to a large excess amount to the number of cysteine residual groups in the sample proteins in a buffer solution of pH 7.0-9.0, and (3) a migration buffer solution both having negative charge while holding SH groups in a migration buffer solution (tris (hydroxymethyl) aminomethane of 25 mM, glycine of 192 mM, (w/v) SDS of 0.1%) of Laemmli method composition, a discontinuous buffer solution of SDS- PAGE, and containing the thiolic reducer to be developed into the gel during electrophoresis.;COPYRIGHT: (C)2004,JPO
机译:解决的问题:对谷物蛋白进行电泳时,要比传统方法在更短的时间内获得清晰的迁移模式。;解决方案:对谷物蛋白进行电泳,具有以下三个基本要素:(1)聚丙烯酰胺凝胶其在水中的最大溶胀度在1.3-2.0之间,(2)用于SDS-PAGE的样品提取物,其中含有巯基还原剂,其对应于缓冲液中样品蛋白质中半胱氨酸残基的数量大大过量pH 7.0-9.0的溶液,以及(3)既带负电荷又保持SH基团在迁移缓冲液(三(羟甲基)氨基甲烷为25 mM,甘氨酸为192 mM,(w / v)SDS为Laemmli方法组合物的0.1%),一种不连续的SDS-PAGE缓冲溶液,并包含在电泳过程中会在凝胶中显影的巯基还原剂。;版权所有:(C)2004,JPO

著录项

  • 公开/公告号JP2003279539A

    专利类型

  • 公开/公告日2003-10-02

    原文格式PDF

  • 申请/专利权人 ATOO KK;

    申请/专利号JP20020121450

  • 发明设计人 OGAWA GOJI;KUBOTA HIDEHIRO;

    申请日2002-03-20

  • 分类号G01N27/447;G01N33/483;G01N33/68;

  • 国家 JP

  • 入库时间 2022-08-22 00:16:59

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