ライフサイエンスコーパス: fluorescamine

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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 nd 1200 m(-1) min(-1), respectively, using a fluorescamine assay.

14 as studied using atomic force microscopy and fluorescamine assays.

15 Because fluorescamine could specifically target the surface amin

16 carboxaldehyde derivative of glycine and the fluorescamine derivative of leucine enkephalin, with the

17 Using fluorescamine derivatization and annexin V binding it wa

18 Fluorescamine derivatization of external aminophospholip

19 sitivity and improved resolution compared to fluorescamine derivatization.

20 Fluorescamine derivatized 3-amino-2,2,5,5,-tetramethyl-1

21 taining detergent (5 min), then labeled with fluorescamine dye (10 s), and analyzed using the microCh

22 This fluorescamine (FSA)-based assay was used to determine th

23 e labeled on their primary amino groups with fluorescamine in a 10-min reaction, and the samples anal

24 s from multiple time points are treated with fluorescamine in a single 96-well plate.

25 ements of two-photon-excited fluorescence of fluorescamine-labeled bradykinin and analysis of multiph

26 yes and nanomolar sensitivity (10(-9) M) for fluorescamine-labeled proteins.

27 Our results demonstrate site-specific fluorescamine labeling at the amino terminus of the 0K-b

28 The results prove that fluorescamine labeling is capable of detecting protein-n

29 Herein, we demonstrated that the fluorescamine labeling method developed by our group not

30 lasm; (ii) release fluorescent material from fluorescamine-labelled cell walls of M. luteus; and (iii

31 hydroxylamine, which can be derivatized with fluorescamine, separated by HPLC and quantified fluorime

32 deacetylation product can be derivatized by fluorescamine, thus generating a fluorescent signal.

33 ect fluorescence produced by the reaction of fluorescamine with hydrolyzed peptides.

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