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1 ight persulfides using the alkylating agent, monobromobimane.
2 pha by measuring the thiol reactivities with monobromobimane.
3  isothiocyanate and is distinct from that of monobromobimane and 1-chloro-2,4 dinitrobenzene.
4 ants were labeled with the fluorescent probe monobromobimane and subjected to an array of fluorescenc
5 known "turn on" fluorescence probe, that is, monobromobimane, and the trapping agent, that is, 2,4-di
6  GST 1-1, the enzyme was further modified by monobromobimane at Cys17 with loss of activity.
7 tivity with 100 microM mycothiol or with the monobromobimane derivative of 1-D-myo-inosityl-2-(L-cyst
8 ity of the NDA method with an assay based on monobromobimane derivatization and HPLC analysis with fl
9 tion of mitochondria with tamoxifen, DTT, or monobromobimane did not reverse the diminished calcium l
10 ith the small, solvent-sensitive fluorophore monobromobimane, exhibit spectral changes only upon bind
11 ts were purified and covalently labeled with monobromobimane fluorescent probe.
12 e show that the steady-state emission from a monobromobimane fluorophore in Loop V-VI is quenched by
13  mutants to react with the fluorescent label monobromobimane followed a similar pattern.
14 ling the cysteines with a fluorescent label (monobromobimane) followed by fluorescence spectroscopic
15 ed cystine for varying periods, treated with monobromobimane, harvested, and extracted with perchlori
16    Wild-type Arabidopsis plants treated with monobromobimane (mBB) form a fluorescent GSH-mBB conjuga
17                                              Monobromobimane (MBB) is a lipophilic reagent that selec
18                                              Monobromobimane (mBBr) can label both Cys111 and Cys17 o
19      Cells were extracted in the presence of monobromobimane (mBBr) to convert thiols to fluorescent
20 maleimidylphenyl)-4-methylcoumarin (CPM), or monobromobimane (mBBr) were used to study the interactio
21 he resulting SonoCage construct reacted with monobromobimane (mBBr), a fluorogenic, thiol-reactive mo
22 gmatis was treated with the alkylating agent monobromobimane (mBBr), the cellular mycothiol was conve
23                                              Monobromobimane (mBrB) showed the highest differential.T
24   The persulfides had higher reactivity with monobromobimane than analogous thiols and putative thiol
25 edoxin are treated with a fluorescent probe (monobromobimane) to label sulfhydryl groups.
26 te and hydrogen peroxide, and with the probe monobromobimane, were studied and compared with those of
27 thod uses a very small cysteine-reactive dye monobromobimane, with virtually no linker, and various t