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Regioselective immobilization of short oligonucleotides to acrylic copolymer gels
Author(s) -
Edward N. Timofeev,
S. V. Kochetkova,
A.D. Mirzabekov,
V. L. Florentiev
Publication year - 1996
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/24.16.3142
Subject(s) - oligonucleotide , acrylamide , aldehyde , regioselectivity , copolymer , polyacrylamide gel electrophoresis , combinatorial chemistry , polyacrylamide , gel electrophoresis , polymer chemistry , chromatography , organic chemistry , chemistry , biochemistry , catalysis , polymer , dna , enzyme
Four types of polyacrylamide or polydimethyl-acrylamide gels for regioselective (by immobilization at the 3' end) of short oligonucleotides have been designed for use in manufacturing oligonucleotide microchips. Two of these supports contain amino or aldehyde groups in the gel, allowing coupling with oligonucleotides bearing aldehyde or amino groups, respectively, in the presence of a reducing agent. The aldehyde gel support showed a higher immobilization efficiency relative to the amino gel. Of all reducing agents tested, the best results were obtained with a pyridine-borane complex. The other supports are based on an acrylamide gel activated with glutaraldehyde or a hydroxyalkyl-functionalized gel treated with mesyl chloride. The use of dimethylacrylamide instead of acrylamide allows subsequent gel modifications in organic solvents. All the immobilization methods are easy and simple to perform, give high and reproducible yields, allow long durations of storage of the activated support, and provide high stability of attachment and low non-specific binding. Although these gel supports have been developed for preparing oligonucleotide microchips, they may be used for other purposes as well.

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