ライフサイエンスコーパス: ethylenediaminetetraacetic acid

1 SauUSI activity was inhibited by ethylenediaminetetraacetic acid.

2 Oligomerisation was reversed by ethylenediaminetetraacetic acid.

3 id, trimethylenediaminetetraacetic acid, and ethylenediaminetetraacetic acid.

4 tion by zinc was reversed in the presence of ethylenediaminetetraacetic acid.

5 P-selectin-bound ligands were eluted with ethylenediaminetetraacetic acid.

6 ours in phosphate-buffered saline with 10 mM ethylenediaminetetraacetic acid.

7 frequency and the inability of the chelator ethylenediaminetetraacetic acid (100 microM) to reverse

8 luoride (1 MBq), (99m)Tc-MDP (1 MBq), (51)Cr-ethylenediaminetetraacetic acid (3 MBq), and (125)I-labe

9 ed with 600 MBq (99m)Tc-MDP and 3 MBq (51)Cr-ethylenediaminetetraacetic acid ((51)Cr-EDTA) and whole-

10 mpounds detected in both WWTP effluents were ethylenediaminetetraacetic acid and 4-nonylphenolethoxyc

11 olinium agents (N-methylglucamine gadolinium ethylenediaminetetraacetic acid and gadolinium trichlori

12 , in a proteolytically "on" state induced by ethylenediaminetetraacetic acid, and in complex with eit

13 cted with 3 MBq (99m)Tc-MDP and 3 MBq (51)Cr-ethylenediaminetetraacetic acid, and multiple blood and

14 ed to DOTA, TETA or 2IT-bromoacetamidobenzyl-ethylenediaminetetraacetic acid (BABE) as coating antige

15 A method for determining EDTA (ethylenediaminetetraacetic acid) based on a highly fluor

16 on competitive reaction between the cadmium-ethylenediaminetetraacetic acid-bovine serum albumin-gol

17 hyde-dimethyl acetate, but not by 1 mM EDTA (ethylenediaminetetraacetic acid), bradykinin 1-5, or ang

18 glomerular filtration rate (mGFR, by chrome-ethylenediaminetetraacetic acid clearance) was associate

19 reagents, such as dipicolinic acid (DPA) and ethylenediaminetetraacetic acid, completely inhibit LpxC

20 The reaction is induced by ethylenediaminetetraacetic acid dipotassium salt dehydra

21 In this study, both ethylenediaminetetraacetic acid (EDTA) and diethylenetri

22 ivo stability over acyclic chelators such as ethylenediaminetetraacetic acid (EDTA) and diethylenetri

23 Multivalent metal chelators, ethylenediaminetetraacetic acid (EDTA) and ethyleneglyco

24 two mild textile extraction methods that use ethylenediaminetetraacetic acid (EDTA) and formic acid a

25 gDNA was extracted from ethylenediaminetetraacetic acid (EDTA) anticoagulant-tre

26 Ascorbic acid (AA) and Ethylenediaminetetraacetic acid (EDTA) are commonly used

27 rates in the presence of the strong chelator ethylenediaminetetraacetic acid (EDTA) but decrease it i

28 s based on integration of signals from metal-ethylenediaminetetraacetic acid (EDTA) complexes at delt

29 -1, whereas reduced Tc(IV) and its humic and ethylenediaminetetraacetic acid (EDTA) complexes show sc

30 In contrast, the addition of disodium ethylenediaminetetraacetic acid (EDTA) elevated the leve

31 Photochemical bleaching in the presence of ethylenediaminetetraacetic acid (EDTA) followed exponent

32 Our work here shows that the use of ethylenediaminetetraacetic acid (EDTA) in DMSO exerts su

33 method for the quantitative determination of ethylenediaminetetraacetic acid (EDTA) in feed and premi

34 this problem using low-molarity solutions of ethylenediaminetetraacetic acid (EDTA) in hydrazine for

35 +)-NTA)(2)-Cy3 binding is reversible in 10mM ethylenediaminetetraacetic acid (EDTA) or 500 mM imidazo

36 R) can accurately be determined using (51)Cr-ethylenediaminetetraacetic acid (EDTA) plasma clearance

37 Ethylenediaminetetraacetic acid (EDTA) plasma showed the

38 via an ultrasound-assisted extraction using ethylenediaminetetraacetic acid (EDTA) producing deterge

39 Both deferoxamine (DFO) and ethylenediaminetetraacetic acid (EDTA) reduced lipid oxi

40 Here, we present a self-powered enzymatic ethylenediaminetetraacetic acid (EDTA) sensor based on t

41 ous paper, treatment of the cellulosome with ethylenediaminetetraacetic acid (EDTA) under aerobic con

42 Pre-incubation of Int with ethylenediaminetetraacetic acid (EDTA) was detrimental f

43 he action of GSH; however, the zinc chelator ethylenediaminetetraacetic acid (EDTA) was ineffective.

44 d PET studies of [11C]TPMP followed by [68Ga]ethylenediaminetetraacetic acid (EDTA) were performed 4

45 Mobile phase A was 20mmolL(-1) ethylenediaminetetraacetic acid (EDTA), 2mmolL(-1) potas

46 g guanidine thiocyanate, ethanol, formamide, ethylenediaminetetraacetic acid (EDTA), and plant-relate

47 Ethylenediaminetetraacetic acid (EDTA), at concentration

48 two known NDM-1 inhibitors, L-captopril and ethylenediaminetetraacetic acid (EDTA), inhibit the hydr

49 plexation with the soluble synthetic ligands ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic

50 Ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic

51 Ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic

52 ), urea, dithiothreitol (DTT), glycerol, and ethylenediaminetetraacetic acid (EDTA), when present as

53 (Res.A) or an ion-releasing resin (Res.B) to ethylenediaminetetraacetic acid (EDTA)-demineralized den

54 uted human whole blood and serum, and HFA in ethylenediaminetetraacetic acid (EDTA)-plasma of patient

55 TFA) or low-molarity (100, 50, 20, and 5 mM) ethylenediaminetetraacetic acid (EDTA).

56 duction) by soluble fibrinogen (3 mg/mL) and ethylenediaminetetraacetic acid (EDTA).

57 ce that could be reversed by the addition of ethylenediaminetetraacetic acid (EDTA).

58 This activity is inhibited by ethylenediaminetetraacetic acid (EDTA).

59 was compared with renal clearance of (51)Cr-ethylenediaminetetraacetic acid (EDTA).

60 ge of the thio analogue in the absence [5 mM ethylenediaminetetraacetic acid (EDTA)] of a divalent me

61 The agents included ethylenediaminetetraacetic acid (EDTA; 10%, pH 7.2), pho

62 NaCl, KCl, Ca-propionate, or FeNa-ethylenediaminetetraacetic acid (FeNa-EDTA) were applied

63 From comparison with time-resolved Fe(II)-ethylenediaminetetraacetic acid footprinting of the modi

64 integrity of the C1 complex (dithiotreitol, ethylenediaminetetraacetic acid, heat inactivation).

65 Finally, ethylenediaminetetraacetic acid is methylated and determ

66 n across the tight junction as observed with ethylenediaminetetraacetic acid or dimethyl sulfoxide tr

67 Induction of the on state by either ethylenediaminetetraacetic acid or the agonist monoclona

68 e wild-type complex in the presence of EDTA (ethylenediaminetetraacetic acid) or Ca(2+), migration wa

69 es repeated agitation of the sample in 0.5 M ethylenediaminetetraacetic acid over a 4-d period.

70 A total of 368 miRNAs were measured in ethylenediaminetetraacetic acid plasma in 10 relapsing-r

71 as extracted from exosomes purified from 152 ethylenediaminetetraacetic acid-plasma samples of 64 pat

72 on linear sucrose gradients with or without ethylenediaminetetraacetic acid, suggesting that GUS ass

73 strongly destabilized by dithiothreitol and ethylenediaminetetraacetic acid, suggesting that metal b

74 g nutrients, boron, bismuth, gadolinium, and ethylenediaminetetraacetic acid) through each major trea

75 LA monoclonal antibody W6/32 in neat normal, ethylenediaminetetraacetic acid-treated normal and compl

76 Only ethylenediaminetetraacetic acid-treated serum MFI was co

77 Ethylenediaminetetraacetic acid was an effective inhibit