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In this process, GO acts with dual functions as a model and a reducing reagent.
Afterward, a reducing reagent of AA was injected, which quickly makes the mixture to be colorless.
Obviously, in this progress a large-scale GO acts with dual functions, as a reducing reagent and a nucleation site of metal or metal oxide nanoparticles.
TCEP·HCl serves as a reducing reagent and can therefore break the disulfide bonds and detach the PFDT coating, along with the B. braunii cells adhered on it.
Au nanoparticles were prepared from hydrogen tetrachloroaurate(III) trihydrate (HAuCl4·3H2O, >98%, Kanto Chemical, Chuo-ku, Tokyo, Japan) as an Au source and trisodium citrate dihydrate (Na-cit, 99%, Kanto Chemical) as a reducing reagent.
Herein, on this basis, we demonstrate a simple hydrothermal method for the synthesis of Ag2Te 1D nanostructures by employing ammonia acting as a complexing reagent and pH regulator hydrazine hydrate (N2H4 · H2O) acting as a reducing reagent.
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Interestingly, molten salt method was not utilized any reducing reagent or other chemicals unless molten silver nitrate.
18 This concept is based on protecting the cysteine residue in the epitope in the form of a disulfide that is liberated, after hypersensitive chemo-exchange, by a mild reducing reagent such as dithiothreitol (DTT) or tris 2-carboxyethyl phosphine (tris 2-carboxyethyl phosphine free cysTCEPe residue witherebyompregenerating integrity.
Interestingly, the reduced form of heteropolyacid can act as a strong reducing reagent which can be readily re-oxidized by various chemicals especially as metal ions [3, 15].
Electrochemically inert tris 2-carboxyethyl phosphine (tris 2-carboxyethyl phosphinereducing reagenTCEP regenerate AA from its oxidation product, thus amplifying the electrochemical signal.
The resulting p-AP could be cycled by a chemical reducing reagent after its electro-oxidization on the electrode (known as p-AP redox cycling), thus enabling an increase in the anodic current.
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