reduction of non-specific protein adsorption using poly(ethylene) glycol (peg) modified polyacrylate hydrogels in immunoassays for staphylococcal enterotoxin b detection减少非特异性蛋白吸附使用聚(乙烯)乙二醇(peg)的改性聚丙烯酸酯水凝胶在免疫测定葡萄球菌肠毒素b检测.pdfVIP

reduction of non-specific protein adsorption using poly(ethylene) glycol (peg) modified polyacrylate hydrogels in immunoassays for staphylococcal enterotoxin b detection减少非特异性蛋白吸附使用聚(乙烯)乙二醇(peg)的改性聚丙烯酸酯水凝胶在免疫测定葡萄球菌肠毒素b检测.pdf

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reduction of non-specific protein adsorption using poly(ethylene) glycol (peg) modified polyacrylate hydrogels in immunoassays for staphylococcal enterotoxin b detection减少非特异性蛋白吸附使用聚(乙烯)乙二醇(peg)的改性聚丙烯酸酯水凝胶在免疫测定葡萄球菌肠毒素b检测

Sensors 2009, 9, 645-655; doi:10.3390/ OPEN ACCESS sensors ISSN 1424-8220 /journal/sensors Article Reduction of Non-Specific Protein Adsorption Using Poly(ethylene) Glycol (PEG) Modified Polyacrylate Hydrogels In Immunoassays for Staphylococcal Enterotoxin B Detection Paul T. Charles*, Veronte R. Stubbs, Carissa M. Soto, Brett D. Martin, Brandy J. White and Chris R. Taitt Center for Bio/Molecular Science and Engineering (Code 6920), US Naval Research Laboratory, 4555 Overlook Ave. SW, Washington, DC 20375, U.S.A. * Author to whom correspondence should be addressed; E-Mail: paul.charles@; Tel.: +1-(202) 404-6064; Fax: +1-(202) 767-1980 Received: 31 October 2008; in revised form: 14 January 2009 / Accepted: 20 January 2009 / Published: 23 January 2009 Abstract: Three PEG molecules (PEG-methacrylate, -diacrylate and -dimethacrylate) were incorporated into galactose-based polyacrylate hydrogels and their relative abilities to reduce non-specific protein adsorption in immunoassays were determined. Highly crosslinked hydrogels containing amine-terminated functionalities were formed and used to covalently attach antibodies specific for staphylococcal enterotoxin B (SEB). Patterned arrays of immobilized antibodies in the PEG-modified hydrogels were created with a PDMS template containing micro-channels for use in sandwich immunoassays to detect SEB. Different concentrations of the toxin were applied to the hydrogel arrays, followed with a Cy3-labeled t

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