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1 pha by measuring the thiol reactivities with monobromobimane.
3 ants were labeled with the fluorescent probe monobromobimane and subjected to an array of fluorescenc
5 tivity with 100 microM mycothiol or with the monobromobimane derivative of 1-D-myo-inosityl-2-(L-cyst
6 ity of the NDA method with an assay based on monobromobimane derivatization and HPLC analysis with fl
7 tion of mitochondria with tamoxifen, DTT, or monobromobimane did not reverse the diminished calcium l
8 ith the small, solvent-sensitive fluorophore monobromobimane, exhibit spectral changes only upon bind
10 e show that the steady-state emission from a monobromobimane fluorophore in Loop V-VI is quenched by
12 ling the cysteines with a fluorescent label (monobromobimane) followed by fluorescence spectroscopic
13 ed cystine for varying periods, treated with monobromobimane, harvested, and extracted with perchlori
14 Wild-type Arabidopsis plants treated with monobromobimane (mBB) form a fluorescent GSH-mBB conjuga
18 maleimidylphenyl)-4-methylcoumarin (CPM), or monobromobimane (mBBr) were used to study the interactio
19 gmatis was treated with the alkylating agent monobromobimane (mBBr), the cellular mycothiol was conve
22 thod uses a very small cysteine-reactive dye monobromobimane, with virtually no linker, and various t
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