ライフサイエンスコーパス: CsCl

1 CsCl abolished the rectification and hyperpolarized the

2 CsCl density gradient centrifugation indicated that almo

3 CsCl thermal ionization data are extremely sensitive to

4 ions of salts of different natures (CaCl(2), CsCl, Na(2)SO(4)) in the same mobile phase agree very we

5 amplification, buoyant density analysis in a CsCl gradient, and immunoprecipitation with monoclonal h

6 We show that in a CsCl gradient, Polycomb response elements, promoters of

7 hree cell types, because of an increase in a CsCl-sensitive, hyperpolarization-activated inward curre

8 triction enzymes, (ii) shift in density on a CsCl gradient of the products synthesized in the presenc

9 ed whole-cell patch electrodes filled with a CsCl-based solution to voltage clamp the currents.

10 green fluorescence under 470 nm light after CsCl purification.

11 s, receptor 3 is able to extract CsNO(3) and CsCl from an aqueous D(2)O layer into nitrobenzene-d(5)

12 ve used glass-fiber filter binding assay and CsCl density gradient ultracentrifugation to monitor the

13 ed both glass fiber filter binding assay and CsCl density gradient ultracentrifugation to monitor the

14 In contrast to what is seen for CsF and CsCl, single-crystal X-ray structural analyses and (1)H

15 on product nanoparticles, including CsOH and CsCl, proceeded via SiO2 condensation over aggregates of

16 s increased linearly with increasing KCl and CsCl concentrations.

17 The abilities of NaCl, KCl, and CsCl to enhance the stability to urea denaturation were

18 of macroscopic I(h), ZD7288 (50 microM) and CsCl (1 mM), reduced the channel conductance to 8 pS and

19 pulsed field gel electrophoresis (PFGE) and CsCl/ethidium bromide equilibrium centrifugation demonst

20 aster, omits the selective precipitation and CsCl gradient steps, uses less expensive and toxic reage

21 ased on the reaction of (SO3CF3)SiH2GeH3 and CsCl.

22 As expected, ZD7288 and CsCl increased latencies and decreased the properties of

23 Other salts, such as CsCl, can give rise to a combination of the two scenario

24 t also synthesized AlNiFe alloy with the B2 (CsCl-type) structure and the metastable Al9Ni2 phase.

25 rent crystal symmetries, including FCC, BCC, CsCl, and AlB2.

26 reported to date binary superlattices (BCC, CsCl, AlB2, Cr3Si, and Cs6C60).

27 ed irreversible and stable to DNA banding by CsCl gradient ultracentrifugation.

28 Somatic I(h) was blocked by CsCl (1 mM) and was partially sensitive to BaCl(2).

29 ard rectification (I(h)) that was blocked by CsCl (3 mM) or by ZD 7288 (30 microM).

30 cells, even when K+ channels were blocked by CsCl and intracellular Na+ was clamped by monensin.

31 This effect was blocked by CsCl and ZD7288, consistent with a role of IH.

32 be effectively separated from each other by CsCl density gradient centrifugation alone.

33 l characterization of viruslike particles by CsCl and sucrose gradient centrifugation revealed biophy

34 t are active at large negative potentials by CsCl and BaCl2, respectively, did not affect DeltaVm, in

35 lary vector in 293 cells and was purified by CsCl banding.

36 tion and size fractionation were purified by CsCl density gradient centrifugation.

37 Ba1 was purified by CsCl gradient centrifugation and was found to have an ic

38 ed into the cell supernatant and purified by CsCl gradient centrifugation.

39 purified from the wild-type helper virus by CsCl equilibrium density-gradient centrifugation and use

40 The cesium chloride (CsCl) density gradient profile of virus particles contai

41 Mucins were isolated by cesium chloride (CsCl) gradient centrifugation and size fractionated on S

42 n be purified by banding in cesium chloride (CsCl) gradients.

43 When the recording pipette contained CsCl, greater peak inward current values and densities w

44 Replacement of pipette solutions containing CsCl with solutions containing equimolar concentrations

45 ied fiber proteins than did the conventional CsCl method.

46 be problematic using conventional two-cycle CsCl gradient ultracentrifugation.

47 DNase, (iii) FeCl3 precipitation and DNase + CsCl and (iv) FeCl3 precipitation and DNase + sucrose.

48 tangential flow filtration (TFF) and DNase + CsCl, (ii) FeCl3 precipitation and DNase, (iii) FeCl3 pr

49 outward currents more effectively than does CsCl.

50 of the transducing particles by equilibrium CsCl density-gradient centrifugation showed that the par

51 sensitive to low concentrations of external CsCl.

52 identical to those where it is observed for CsCl and CsBr.

53 h maximizes the recovery of labeled DNA from CsCl gradients.

54 indicate that the CuAu-I crystals form from CsCl parent crystals by a diffusionless transformation,

55 les into different crystal structures, e.g., CsCl, AlB2, and Cr3Si.

56 Similar disparities in CsCl sensitivity were observed in myocytes isolated from

57 ent sedimentation equilibrium experiments in CsCl with UV detection were also generated.

58 dye binds to the negatively charged GAGs in CsCl-fractionated extracts from chicken tendons.

59 yant density of the cross-linked particle in CsCl led to the total mass of the particles and their fr

60 yant density of the cross-linked particle in CsCl we could deduce the total mass of the particle, hen

61 A comparison of proteins in CsCl density gradient centrifugation fractions from supe

62 how that this mineral should dissociate into CsCl-type MgO cotunnite-type SiO2 at pressures and tempe

63 from the medium of Sf9 cultures by isopycnic CsCl gradient centrifugation followed by rate-zonal cent

64 In 1.0 M CsCl, the conductance of each analogue channel is approx

65 eld the intrinsic pKain of PS lipid in 0.1 M CsCl to be in the range 2.5-3.0.

66 M NaCl, 30% ammonium sulfate (mu = 7.0); 3 M CsCl, 30% ammonium sulfate (mu = 7.0); and 2.5 M NaCl, 3

67 It was blocked by external perfusion of 1 mM CsCl but was unaffected by BaCl(2).

68 The micropipette contained 130 mM CsCl and 1 microM QX-314.

69 asured with patch pipettes containing 130 mM CsCl was 10-15 pS (n = 15 cell pairs); despite this low

70 sured using patch pipettes containing 130 mM CsCl was 220 +/- 13.1 pS (12 cell pairs).

71 under voltage clamp in the presence of 15 mM CsCl and 15 mM tetraethylammonium chloride (TEA-Cl) to e

72 1,000 picosiemens (pS) in symmetrical 150 mm CsCl were observed.

73 (G-T)] and poly[d(A-T)].poly[d(A-T)] in 5 mM CsCl, 0.2 mM HEPES, pH 7.5 at 20 degrees C.

74 naturing conditions in the presence of NaCl, CsCl, and tetrabutyl ammonium chloride (NBu4Cl).

75 mes increase by a factor of 2 on addition of CsCl as the electrolyte.

76 In the case of CsCl, an unprecedented 2:2 complex is observed in the so

77 th groups then received incremental doses of CsCl until sustained VT resulted.

78 by isopycnic centrifugation in a mixture of CsCl and guanidine HCl.

79 rizing current injections in the presence of CsCl.

80 e purified from Extract PBS by two rounds of CsCl/guanidine HCl ultracentrifugation as well as in vit

81 en PTX3 and AM HC-HA withstands four runs of CsCl ultracentrifugation in the presence of 4 m GnHCl.

82 VC2.null) were isolated by sequential use of CsCl step gradients followed by isopycnic centrifugation

83 With 1 mEq/kg body weight of CsCl, MAPD90 rose by 86 +/- 100 ms in dogs with HF versu

84 d to high titer (> 10(8)/ml) and purified on CsCl gradients due to their buoyancy difference relative

85 mm (where m denotes molality) NaCl, KCl, or CsCl.

86 In current-clamp recording, CsCl, which inhibits only I(H) in nodose neurons, hyperp

87 stable complexes with the test cesium salts, CsCl and CsNO(3), in solution (10% methanol-d(4) in chlo

88 es suspended in different density solutions, CsCl for microbeads and Percoll for cells.

89 In symmetrical CsCl solutions with minimal concentrations of internal E

90 At the sensory receptor terminal, CsCl decreased the threshold pressure for initiation of

91 luid, but does have a lower free energy than CsCl.

92 We found that CsCl induced larger early afterdepolarizations and a gre

93 The CsCl sensitivity of this mutant is suppressed by recessi

94 perstructures: a superatomic relative of the CsCl lattice type and an unusual packing arrangement bas

95 repolarization and heightened sensitivity to CsCl at chamber and cellular levels.

96 were purified from Syn5-infected cells using CsCl centrifugation followed by sucrose gradient centrif

97 Cells were voltage clamped using CsCl filled electrodes, while action potentials and exci

98 negative-strand viral RNA was detected using CsCl-purified CVB3/TD virions, although no negative-stra

99 isera to known proteoglycans; purified using CsCl density gradient centrifugation, molecular sieve, a

100 the P(o) at depolarized potentials, whereas CsCl was more efficacious at hyperpolarized potentials.

101 We further tested whether CsCl inhibition of repolarizing K+ currents, which are r

102 tanoyl phosphatidylserine (PS) bilayers with CsCl aqueous solutions, we show that the effects of lipi

103 by increased temperature in combination with CsCl or with NaCl plus an alpha subunit ligand, alpha-gl

104 either compositionally ordered crystals with CsCl and CuAu-I symmetries, or disordered, solid solutio

105 In contrast to findings with CsCl, when organic ions were used in the pipette solutio

106 l layer V pyramidal cells were recorded with CsCl electrodes.

107 Ba(2+), and also reduced in recordings with CsCl-containing electrodes, suggesting a dual underlying

108 I(K1) suppression with CsCl (5 mmol/L, n=3), BaCl(2) (3 micromol/L, n=3), and l