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一种用于多重复制技术及在微型二维凝胶上鉴定人血清蛋白的电转印装置。

An electroblotting apparatus for multiple replica technique and identification of human serum proteins on micro two-dimensional gels.

作者信息

Manabe T, Takahashi Y, Okuyama T

出版信息

Anal Biochem. 1984 Nov 15;143(1):39-45. doi: 10.1016/0003-2697(84)90555-4.

DOI:10.1016/0003-2697(84)90555-4
PMID:6084965
Abstract

A new apparatus for electrophoretic transfer of proteins from micro polyacrylamide slab gels has been developed. The apparatus enabled the easy changing of nitrocellulose sheets and was suited for obtaining multiple blots from a gel. Electrophoretic conditions were determined so that all of the blots obtained sequentially from one slab gel were successfully used to visualize specific proteins irrespective of their molecular weight. Combining the transfer technique with the technique of parallel micro two-dimensional electrophoresis, 20 blots could be obtained within 1 h of electroblotting time. The locations of 28 human serum proteins were determined simultaneously on these blots using commercial specific antisera.

摘要

一种用于将蛋白质从微量聚丙烯酰胺平板凝胶中进行电泳转移的新装置已被开发出来。该装置能够轻松更换硝酸纤维素膜,并且适合从一块凝胶上获得多个印迹。确定了电泳条件,以便从一块平板凝胶上依次获得的所有印迹都能成功用于可视化特定蛋白质,而不论其分子量大小。将转移技术与平行微量二维电泳技术相结合,在1小时的电印迹时间内可获得20个印迹。使用市售的特异性抗血清在这些印迹上同时确定了28种人血清蛋白的位置。

相似文献

1
An electroblotting apparatus for multiple replica technique and identification of human serum proteins on micro two-dimensional gels.一种用于多重复制技术及在微型二维凝胶上鉴定人血清蛋白的电转印装置。
Anal Biochem. 1984 Nov 15;143(1):39-45. doi: 10.1016/0003-2697(84)90555-4.
2
Electroblotting of multiple gels: a simple apparatus without buffer tank for rapid transfer of proteins from polyacrylamide to nitrocellulose.多凝胶的电转印:一种无需缓冲槽的简易装置,用于将蛋白质从聚丙烯酰胺快速转移至硝酸纤维素膜。
J Biochem Biophys Methods. 1984 Dec;10(3-4):203-9. doi: 10.1016/0165-022x(84)90040-x.
3
Double replica electroblotting: a method to produce two replicas from one gel.双重复制电转印法:一种从一块凝胶制备两个复制品的方法。
J Biochem Biophys Methods. 1986 Nov;13(4-5):197-203. doi: 10.1016/0165-022x(86)90098-9.
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Semidry electroblotting of peptides and proteins from acid-urea polyacrylamide gels.从酸性尿素聚丙烯酰胺凝胶中对肽和蛋白质进行半干法电印迹
Anal Biochem. 1997 Nov 15;253(2):225-30. doi: 10.1006/abio.1997.2347.
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Quantitative electrophoretic transfer of DNA from polyacrylamide or agarose gels to nitrocellulose.DNA从聚丙烯酰胺或琼脂糖凝胶到硝酸纤维素膜的定量电泳转移。
Anal Biochem. 1984 Feb;137(1):120-4. doi: 10.1016/0003-2697(84)90356-7.
6
Silver staining of proteins on electroblotting membranes and intensification of silver staining of proteins separated by polyacrylamide gel electrophoresis.蛋白质在电转印膜上的银染以及聚丙烯酰胺凝胶电泳分离的蛋白质银染的增强。
Anal Biochem. 2002 May 1;304(1):33-41. doi: 10.1006/abio.2001.5604.
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Transfer of proteins from acrylamide gels to nitrocellulose paper after silver stain detection.银染检测后将蛋白质从丙烯酰胺凝胶转移至硝酸纤维素膜上。
J Immunol Methods. 1988 Feb 24;107(1):143-9. doi: 10.1016/0022-1759(88)90020-8.
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Electroblotting of proteins from polyacrylamide gels.
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"High-resolution" mini-two-dimensional gel electrophoresis automatically run and stained in less than 6 h with small, ready-to-use slab gels.
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Efficacy of passive transfer of proteins from preparative polyacrylamide gels to nitrocellulose membranes.蛋白质从制备型聚丙烯酰胺凝胶被动转移至硝酸纤维素膜的效果。
Indian J Biochem Biophys. 1995 Oct;32(5):245-8.

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