Liposome-Assisted Enzymatic Modulation of Plasmonic Photoelectrochemistry for Immunoassay was written by Chen, Feng-Zao;Han, De-Man;Chen, Hong-Yuan. And the article was included in Analytical Chemistry (Washington, DC, United States) in 2020.Recommanded Product: (2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate The following contents are mentioned in the article:
Recently emerged liposomal photoelectrochem. (PEC) bioanal. has brought new opportunities for biosensor development. This work presents the new concept of liposome-assisted enzymic modulation of plasmonic photoelectrochem. for PEC bioanal., which was exemplified by an Au nanoclusters (NCs)-sensitized nanoporous TiO2 nanotubes (Au NC@TiO2 NT) photoelectrode and an alk. phosphatase (ALP)-loaded liposomal immunoassay of heart-type fatty acid binding protein in a 96-well plate. After sandwich immunorecognition and subsequent lysis treatment, enzymically generated ascorbic acid by the released ALP was directed to reduce Au3+ into Au nanoparticles using the Au NCs as seeds, leading to the in situ change of the photoelectrochem. of the electrode and corresponding reduction of the photocurrent. The depressed signal could be correlated with the target concentration with good anal. performance in terms of sensitivity and selectivity. This work features the liposome-assisted enzymic modulation of plasmonic photoelectrochem., which provides a new protocol for general PEC bioanal. development. This study involved multiple reactions and reactants, such as (2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5Recommanded Product: (2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate).
(2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: (2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate
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