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231224s2012 xx |||||o 00| ||eng c |
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|a 10.1021/la303032f
|2 doi
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|a pubmed24n0744.xml
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|a (DE-627)NLM223167797
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|a (NLM)23210719
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|a DE-627
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|c DE-627
|e rakwb
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|a eng
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| 100 |
1 |
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|a Niu, Yu
|e verfasserin
|4 aut
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| 245 |
1 |
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|a Antibody oriented immobilization on gold using the reaction between carbon disulfide and amine groups and its application in immunosensing
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|c 2012
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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| 338 |
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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| 500 |
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|a Date Completed 23.05.2013
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|a Date Revised 21.11.2013
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Carbon disulfide (CS(2)) can spontaneously react with amine groups to form dithiocarbamates on gold surface, providing the possibility to immobilize some compounds with primary or secondary amine groups in one step. Using this principle, an immunosensor interface prepared for immunoglobulin G (IgG) sensing surface toward anti-IgG has been fabricated for the first time by simply immersing gold slides into a mixed aqueous solution of CS(2) and protein A, followed by incubation in immunoglobulin G solution. The reaction between CS(2) and protein A has been followed by UV-vis spectroscopy, whereas cyclic voltammetry has been employed in the characterization of the modified gold surface with CS(2) and protein A, both methods indicating that protein A immobilization is implemented by CS(2). Conventional ellipsometry, atomic force microscopy (AFM), as well as surface plasmon resonance (SPR) have been used to evaluate the specific binding of protein A with IgG and IgG with anti-IgG, revealing that IgG is specifically captured to form the biosensing interface, maintaining its bioactivity. Compared to direct adsorption of IgG on the gold surface, the IgG sensing surface constructed of CS(2) and protein A is far more sensitive to capture anti-IgG as its target molecule. In addition, the modified surface is proven to have good capability to inhibit nonspecific adsorption, as supported by control experiments using lysozyme and BSA. To conclude, antibody immobilization using this one-step method has potential as a simple and convenient surface modification approach for immunosensor development
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Amines
|2 NLM
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|a Immobilized Proteins
|2 NLM
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|a Immunoglobulin G
|2 NLM
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|a Staphylococcal Protein A
|2 NLM
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|a Gold
|2 NLM
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| 650 |
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|a 7440-57-5
|2 NLM
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| 650 |
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|a Carbon Disulfide
|2 NLM
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| 650 |
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|a S54S8B99E8
|2 NLM
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| 700 |
1 |
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|a Matos, Ana I
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Abrantes, Luisa M
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Viana, Ana S
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Jin, Gang
|e verfasserin
|4 aut
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| 773 |
0 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 28(2012), 51 vom: 21. Dez., Seite 17718-25
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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| 773 |
1 |
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|g volume:28
|g year:2012
|g number:51
|g day:21
|g month:12
|g pages:17718-25
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|u http://dx.doi.org/10.1021/la303032f
|3 Volltext
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