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  • Direct biomolecule binding on nonfouling surfaces via newly discovered supramolecular self-assembly of lysozyme under physiological conditions.

Direct biomolecule binding on nonfouling surfaces via newly discovered supramolecular self-assembly of lysozyme under physiological conditions.

Macromolecular bioscience (2012-06-19)
Peng Yang
ZUSAMMENFASSUNG

When lysozyme is dissolved in a neutral HEPES buffer solution (pH = 7.4) with 0.001-0.050 M TCEP added, a fast phase transition process occurs and the resulting novel fiber-like hierarchical supramolecular assemblies made by primary spherical-particle aggregation can function as a "superglue" that binds strongly and quickly onto non-fouling coatings. This binding is highly selective towards lysozyme, and excludes synthetic, chemical/physical activation/deactivation (blocking) steps. By using biotinylated lysozyme, such a phase transition quickly creates a perfect biotinylated surface on non-fouling surfaces for avidin binding, showing great potential for the development of low-cost and practical biochips.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
HEPES, ≥99.5% (titration)
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HEPES -Lösung, 1 M, pH 7.0-7.6, sterile-filtered, BioReagent, suitable for cell culture
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HEPES-Pufferlösung, 1 M in H2O
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HEPES -Lösung, BioPerformance Certified, 1 M, suitable for cell culture, 0.2 μm filtered
SAFC
HEPES
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HEPES, BioXtra, pH 5.0-6.5 (1 M in H2O), ≥99.5% (titration)
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HEPES Natriumsalz -Lösung, 1M, BioReagent, suitable for cell culture
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HEPES Natriumsalz, ≥99.5% (titration), free-flowing, Redi-Dri