Synthesis of hydrogel via click chemistry for DNA electrophoresis
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作者:
Finetti, Chiara
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Natl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, ItalyNatl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, Italy
Finetti, Chiara
[1
]
Sola, Laura
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Natl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, ItalyNatl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, Italy
Sola, Laura
[1
]
Elliott, Jim
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Agilent Technol R&D & Mkt GmbH & Co KG, Hewlett Packard Str 8, D-76337 Waldbronn, GermanyNatl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, Italy
Elliott, Jim
[2
]
Chiari, Marcella
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Natl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, ItalyNatl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, Italy
Chiari, Marcella
[1
]
机构:
[1] Natl Res Council Italy, Inst Chem Mol Recognit, Via Mario Bianco 9, I-20131 Milan, Italy
This work introduces a novel sieving gel for DNA electrophoresis using a classical click chemistry reaction, the copper (I)-catalyzed azide-alkyne cycloaddition (CuAAC), to cross-link functional polymer chains. The efficiency of this reaction provides, under mild conditions, hydrogels with near-ideal network connectivity and improved physical properties. Hydrogel formation via click chemistry condensation of functional polymers does not involve the use of toxic monomers and IN initiation. The performance of the new hydrogel in the separation of double stranded DNA fragments was evaluated in the 2200 TapeStation system, an analytical platform, recently introduced by Agilent that combines the advantages of CE in terms of miniaturization and automation with the simplicity of use of slab gel electrophoresis. The click gel enables addition of florescent dyes prior to electrophoresis with considerable improvement of resolution and separation efficiency over conventional cross-linked polyacrylamide gels. (C) 2017 Elsevier B.V. All rights reserved.