2010•Journal of Jinan UniversityRequires access

Amination of epoxy-containing agarose as a gene transfection vector

Shunqing Tang

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Abstract

Agarose was degraded by oxidation,activated by chloroepoxypropane,and then aminated with ethylenediamine to introduce amino groups into agarose chain.Finally,the aminated agarose was combined to pEGFP-C1 plasmid.The infrared spectrophotometry analysis(IR),element analysis(EA),agarose gel electrophoresis,particle size and zeta potential analysis were carried out to characterize the as-prepared aminated agaorse and its application as a gene vector.The results of IR and EA showed that the agarose succeeded to be grafted with amino groups.The agarose gel electrophoresis showed that aminated agarose could effectively protect the pEGFP-C1 plasmid.The results provided a reasonable basis for the preparation of gene vector using aminated agarose.

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What this paper is about

Agarose was degraded by oxidation,activated by chloroepoxypropane,and then aminated with ethylenediamine to introduce amino groups into agarose chain.Finally,the aminated agarose was combined to pEGFP-C1 plasmid.The infrared spectrophotometry analysis(IR),element analysis(EA),agarose gel electrophoresis,particle size and zeta potential analysis were carried out to characterize the as-prepared aminated agaorse and its application as a gene vector.The results of IR and EA showed that the agarose succeeded to be grafted with amino groups.The agarose gel electrophoresis showed that aminated agarose could effectively protect the pEGFP-C1 plasmid.The results provided a reasonable basis for the preparation of gene vector using aminated agarose.

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Available abstract

Agarose was degraded by oxidation,activated by chloroepoxypropane,and then aminated with ethylenediamine to introduce amino groups into agarose chain.Finally,the aminated agarose was combined to pEGFP-C1 plasmid.The infrared spectrophotometry analysis(IR),element analysis(EA),agarose gel electrophoresis,particle size and zeta potential analysis were carried out to characterize the as-prepared aminated agaorse and its application as a gene vector.The results of IR and EA showed that the agarose succeeded to be grafted with amino groups.The agarose gel electrophoresis showed that aminated agarose could effectively protect the pEGFP-C1 plasmid.The results provided a reasonable basis for the preparation of gene vector using aminated agarose.

Key concepts: Agarose, Agarose gel electrophoresis, Color marker, Chemistry, Ethylenediamine, Amination, Plasmid, Zeta potential

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