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1 uorescence detection after derivatizing with fluorescamine.
2 maller peptides or of new amino groups using fluorescamine.
3 on was confirmed by end group analysis using fluorescamine.
4 oxide that was subsequently derivatized with fluorescamine.
5 mploying a previous derivatisation step with fluorescamine.
6 3-ap) alone, followed by derivatization with fluorescamine.
7                            The assay employs fluorescamine, a primary-amine specific fluorogenic dye,
8       The modified receptor was labeled with fluorescamine, an amine-reactive fluorescent probe.
9                                        While fluorescamine and naphthalene-2,3-dicarboxaldehyde (NDA)
10      To this end, here we describe optimized fluorescamine and NDA derivatization reactions that enha
11                  In principle, the optimized fluorescamine and NDA microplate procedures reported her
12                                     For both fluorescamine and NDA, we have shown that the RFI values
13 ydroxylamine, which is then derivatized with fluorescamine and quantified spectrofluorometrically.
14 nd 1200 m(-1) min(-1), respectively, using a fluorescamine assay.
15 as studied using atomic force microscopy and fluorescamine assays.
16                                      Because fluorescamine could specifically target the surface amin
17 carboxaldehyde derivative of glycine and the fluorescamine derivative of leucine enkephalin, with the
18                                        Using fluorescamine derivatization and annexin V binding it wa
19                                              Fluorescamine derivatization of external aminophospholip
20 sitivity and improved resolution compared to fluorescamine derivatization.
21                                              Fluorescamine derivatized 3-amino-2,2,5,5,-tetramethyl-1
22 taining detergent (5 min), then labeled with fluorescamine dye (10 s), and analyzed using the microCh
23                                         This fluorescamine (FSA)-based assay was used to determine th
24 e labeled on their primary amino groups with fluorescamine in a 10-min reaction, and the samples anal
25 s from multiple time points are treated with fluorescamine in a single 96-well plate.
26 ements of two-photon-excited fluorescence of fluorescamine-labeled bradykinin and analysis of multiph
27 yes and nanomolar sensitivity (10(-9) M) for fluorescamine-labeled proteins.
28        Our results demonstrate site-specific fluorescamine labeling at the amino terminus of the 0K-b
29                       The results prove that fluorescamine labeling is capable of detecting protein-n
30             Herein, we demonstrated that the fluorescamine labeling method developed by our group not
31 lasm; (ii) release fluorescent material from fluorescamine-labelled cell walls of M. luteus; and (iii
32 hydroxylamine, which can be derivatized with fluorescamine, separated by HPLC and quantified fluorime
33  deacetylation product can be derivatized by fluorescamine, thus generating a fluorescent signal.
34 ect fluorescence produced by the reaction of fluorescamine with hydrolyzed peptides.