ライフサイエンスコーパス: buffer system

1 nd pH conditions using a lactic acid/lactate buffer system.

2 D(50)/mL for toxin types A, B, E, and F in a buffer system.

3 ke structures through the use of a high salt buffer system.

4 ier employed in the eluent and the pH of the buffer system.

5 ayer chromatography (TLC) with the specified buffer system.

6 olar protic/aprotic media, including aqueous buffer systems.

7 sequentially extracted with three different buffer systems.

8 d I/O curve into a double-sigmoid typical of buffer systems.

9 in both sulfonic acid and acetate-containing buffer systems.

10 imes more soluble than paclitaxel in various buffer systems.

11 ditions close to reality, instead of simpler buffer systems.

12 d by isothermal titration calorimetry in two buffer systems.

13 ride (LPS) dispersions, and trifluoroethanol buffer systems.

14 +) ions was established using an EDTA-Mg(2+) buffered system.

15 ow-gated glutamate receptor and/or glutamate buffering system.

16 ondria is bound by intramitochondrial Ca(2+) buffering systems.

17 rylamide gel electrophoresis in 10 different buffer systems (1) was replaced by a greatly simplified

18 Using boric acid and TES buffer systems, 500 microm was determined to be the opti

19 ation in the model wine system, while in the buffer system a reducing effect is observed.

20 Alteration of the pH of the buffer system affects the heme iron spin-state equilibri

21 urst release in a pH 9.0 NaHCO(3)-Na(2)CO(3) buffer system and a gradual release in pH 7.4 simulated

22 and related cellular metabolites in various buffer systems and find that oxygen has a profound effec

23 tides and proteins at a given pH in standard buffer systems and validated the sorting result with LC/

24 most significantly by the cytosolic calcium buffering system and changes in diastolic Ca(2+) .

25 ed nitrocellulose membrane using a phosphate buffer system, and stained and developed using the same

26 t that incorporates diffusion, intracellular buffering systems, and stochastically gated ion channels

27 Our results demonstrate that distinct buffering systems are dedicated to particular Ca(2+) sou

28 NA structure eventually converges in the two buffer systems, as the divalent ion concentration approa

29 A MES/TRIS buffer system at pH 6.1 eliminates the need for surface

30 a brucei TryS in a newly developed phosphate buffer system at pH 7.0 and 37 degrees C, mimicking the

31 r physiological conditions (phosphate-saline buffer system at pH 7.4 and 37 degrees C), using vesicle

32 ake use of purified macromolecules in simple buffer systems at concentrations that range from micromo

33 lular superfusate with a 5 % CO(2)/HCO(3)(-) buffer system (at constant pH(o) of 7.40).

34 Interestingly, comparative analysis of two buffer systems (based on acetic acid vs citric acid) rev

35 Gels using a discontinuous buffer system but which do not have a separate stacking

36 on the pH change occurring in an appropriate buffer system by the concomitant release of H(+) during

37 a(2+) influx and regulated by a large Ca(2+) buffering system, Ca(2+) extrusion via a PMCA and Ca(2+)

38 ve Ca2+ influx and regulated by a large Ca2+ buffering system, Ca2+ extrusion via a PMCA and Ca2+ tra

39 Simple buffer systems can be used, and the concentration result

40 Although the contribution of Ca(2+) buffering systems can vary between neuronal types and ce

41 ally as well as experimentally for the model buffer system composed of benzoic acid/LiOH or common bu

42 The optimal buffer system conditions, which maximized the IgE-bindin

43 effects can be complex, especially when the buffer systems contain many ionic components.

44 If the RBC buffer system contained 2.5 mM EGTA, PS exposure also de

45 olation of intact Sauromatum rRNA requires a buffer system containing a high amount of the chelator E

46 The method utilizes an optimized buffer system containing a linear pentylamine and a uniq

47 avage of E298D was eliminated using a sample buffer system designed to limit acidic hydrolysis of Asp

48 were only insignificantly influenced by the buffer system except for citrate and phosphate buffers,

49 e Ca(2+) transport, the intracellular Ca(2+) buffering systems expressed in ameloblasts and provides

50 The use of a compatible buffer system for all enzymes allows the reaction to be

51 the optimization and utilization of a novel buffer system for fast DNA separations by capillary and

52 Creatine and creatine phosphate act as a buffer system for the regeneration of ATP in tissues wit

53 emediation by providing microbially mediated buffering systems for the associated microbial and/or ch

54 The discontinuous buffer system forms highly enriched analyte zones outsid

55 and nuclear proteins in the three respective buffer system fractions.

56 ive stress, cells are equipped with reducing buffer systems (glutathione/GSH and thioredoxin/thioredo

57 atic, either methanol- or acetonitrile-based buffer systems, HPLC elution into an LTQ mass spectromet

58 rst evidence of a reverberating input-output buffer system in the dorsal stream underlying speech sen

59 2)(+) because of the introduction of an EDTA buffer system in the revised medium.

60 n of dansyl-YVG was studied in two different buffer systems in the pH range of 4-10.

61 ng the effects of the endogenous bicarbonate buffering system in evaluating the function of prestin i

62 lutathione and GSSG form the principle redox buffering system in the cell, with the endoplasmic retic

63 nimals have an effective oxidation-reduction buffering system in the liver that provides protection f

64 Different gel buffer systems, including a modified polyacrylamide gel

65 s' shift of 94 nm, and their fluorescence in buffer systems increased with pH values from neutral to

66 The Triton X-100-activated MPP is pH-, buffer system-, ionic strength-, and temperature-depende

67 h3N surface concentration assayed in pH 10.0 buffer system is 9 times greater than that at pH 7.4.

68 An additional benefit with this buffer system is the low current observed at high fields

69 The critical difference between these two buffering systems is that islets maintain a lower intrac

70 ne unit lower that of the separation and gel buffer system makes possible efficient stacking of the D

71 Using the 100 mM KPO4 buffer system, nitrate levels were determined following

72 In boric acid (80mM, pH 8.0) running buffer system, not only were alpha and beta-ODAP success

73 asured partition coefficient in an n-octanol/buffer system of AMPO was similar to those of DMPO and D

74 h resolving capacity of the Tris-Tricine-SDS buffer system of Schaegger and von Jagow we were able to

75 This highly buffered system of ABA metabolism represents both a chal

76 the effects of bicarbonate/CO2 and phosphate buffer systems on metal ion-catalyzed oxidation of LDL t

77 e (41.6 g/L) from 500 mM citrate without any buffer system or additional cofactors, with 64.0% conver

78 on when NZVI technology is applied to poorly buffered systems, particularly at a low amount of NZVI (

79 as greater than that obtained in a phosphate buffer system (PBS).

80 of cross-linking and use of the clear native buffer system performs well for both fractionation and n

81 US on lactulose formation, in general, in a buffered system (pH 10.0), US at 70% of amplitude and 60

82 Phosphagen energy-buffering systems play an essential role in regulating t

83 ction, electrokinetic injection with this CE buffer system provided substantially lower detection lim

84 e development of system peaks in interacting buffer systems significantly differs from the behavior k

85 uWestern) using a Tris tricine discontinuous buffer system suitable for analyses of a wide molecular

86 ovided by the implementation of a particular buffer system that is designed to initially function in

87 To identify a purification buffer system that maintained the receptor in a nonaggre

88 e glutathione pathway, an efficient cellular buffering system that counteracts reactive oxygen specie

89 parvalbumin are part of the cellular calcium buffering system that determines intracellular calcium d

90 together, these results show that there is a buffering system that regulates the number of Shh-expres

91 support a model in which LDs provide a lipid buffering system that sequesters FAs released during the

92 o experiments were carried out in an aqueous buffer system to determine the reactivity of nucleophili

93 dimension capillary contains an SDS-pullulan buffer system to perform capillary sieving electrophores

94 rforming ITP-AC and describe the design of a buffer system to perform sequence specific separation of

95 s also applied to fractionations in a single buffer system to which various combinations of ionic and

96 mRNPs and establishes a post-transcriptional buffering system to facilitate SSC homeostasis in the fl

97 H1 by about 0.4 pH units, independent of the buffer system used.

98 mine parabolic flow due to the discontinuous buffer systems used for sample stacking.

99 unique in that it works with typical acidic buffer systems used in electrospray ionization, making i

100 scontinuous gel electrophoresis in an acidic buffer system using the cationic detergent benzyldimethy

101 Formation of the acid SC-buffer system was accelerated by topically applying the

102 A hybrid buffer system was developed, in which both the depositio

103 t agarose types, agarose concentrations, and buffer systems was determined.

104 were collected in the same lipid bilayer and buffer system we previously used to determine those para

105 Two alternative "pK-matched" buffer systems were substituted for the traditionally us

106 The CE method uses an attractive buffer system which is highly stable and inexpensive, an

107 ional interplay between Ca(2+) transport and buffering systems whose activities depend nonlinearly on

108 yacrylamide gel electrophoresis in different buffer systems with the purpose of optimizing the operat

109 )]i ~ 1 micro M, and to involve at least two buffering systems with different affinities for Ca(2+).

110 roximately 1 pM, and to involve at least two buffering systems with different affinities for Ca2+.

111 ensitivity of 10(3) CFU/mL of V. cholerae in buffer system within 4 h.

112 e saturation, but rather reflects a powerful buffering system within the mitochondrial matrix.

113 a given pH) of peptides and dyes in standard buffer systems without using sheath flows.