Amination of epoxy-containing agarose as a gene transfection vector
Shunqing Tang
Abstract
Shunqing Tang
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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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