1 oethyl)carbamyl] GTP (edGTP), and adducts of fluorescein 5-isothiocyanate and rhodamine B-isothiocyan

2 abeled with 1-aminopyrene as donor probe and fluorescein-5-isothiocyanate as acceptor probe attached

3   Consistent with this idea, the reaction of fluorescein 5'-isothiocyanate at Lys-474 was also stimul

4 thalene-1-sulfonic acid) and acceptor (i.e., fluorescein 5-isothiocyanate) chromophores covalently bo

5  tetramethylrhodamine succidimidyl ester and fluorescein-5-isothiocyanate derivatized amino acids.

6                             Experiments with fluorescein 5'-isothiocyanate (FITC)-labelled ATPase als

7                    Previous studies in which fluorescein 5-isothiocyanate (FITC) was used to label th

8    Progressive modification of Lys(514) with fluorescein 5-isothiocyanate (FITC), which physically bl

9  a luminal IgG epitope to allow targeting of fluorescein-5'-isothiocyanate (FITC)-labeled anti-IgG F(

10 I), FRET measurements were carried out using fluorescein-5-isothiocyanate (FITC) as donor and tetrame

11                               Green-emitting fluorescein-5-isothiocyanate (FITC) was conjugated to th

12  was improved by 94-, 108-, and 160-fold for fluorescein-5-isothiocyanate, fluorescein disodium, and

13 he most popular reagents for P-type ATPases (fluorescein 5'-isothiocyanate) has been developed.

14                              Fluorescence of fluorescein 5-isothiocyanate-labeled SR suggests that C2

15                                              Fluorescein 5-isothiocyanate was attached to Amino-Modif

16 oted entry of the large (>1 nm) negative dye fluorescein-5-isothiocyanate while decreasing entry of t