ライフサイエンスコーパス: constant temperature

1 ndred millivolts, we can trigger IM-PCR at a constant temperature.

2 ent with variations in mantle composition at constant temperature.

3 that undergo exponential amplification at a constant temperature.

4 inment to thermocycles versus photocycles in constant temperature.

5 ected scaling of metabolic rate with size at constant temperature.

6 racy comparable to the results obtained at a constant temperature.

7 y monitoring fluorescence at each cycle at a constant temperature.

8 dry weight as compared with those under the constant temperature.

9 sects that diverge from those predicted from constant temperatures.

10 e 'fundamental' norms derived under standard constant temperatures.

11 na for circadian leaf movement at a range of constant temperatures.

12 nted growth under continuous irradiation and constant temperatures.

13 s, our simulations used an atom-based model, constant temperature (274 K), and non-beta-hairpin initi

14 ric fields at a low field strength (0.4V/cm) constant temperature (65 degrees C) has a statistically

15 y increasing the additive concentration at a constant temperature and by increasing temperature at a

16 conditions can be controlled by pressure, at constant temperature and flow rate.

17 The constant temperature and pressure algorithm of the AMBER

18 We report the results of constant temperature and pressure molecular dynamics cal

19 length were carried out under conditions of constant temperature and pressure using periodic boundar

20 d classical molecular dynamics simulation at constant temperature and pressure with explicit solvent

21 gh typically cosseted in the laboratory with constant temperatures and plentiful nutrients, microbes

22 constant conditions (continuous darkness and constant temperature) and is eliminated by period gene n

23 curves of helix formation induced by TFE at constant temperature, and the properties of these helix

24 ity along Earth's surface needed to maintain constant temperatures, and has a global mean of 0.42 km

25 To evaluate the constant temperature assumption in our experiments, the

26 In the present apparatus, water, at a constant temperature between 3 and 60 degrees C, is circ

27 arrest with an initial shockable rhythm at a constant temperature between 32 degrees C and 36 degrees

28 red as a function of lipid molecular area at constant temperatures between 10 degrees C and 30 degree

29 function of lipid molecular area at various constant temperatures between 10 degrees C and 30 degree

30 support of these findings, saplings grown at constant temperature but exposed to an extended photoper

31 e when incubated for 21 days at 20 degrees C constant temperatures, but nearly 30% germinate after 21

32 rification in an aged woodchip bioreactor at constant temperature can effectively be modeled using ze

33 surement of NOE effects, 3JHN alpha coupling constants, temperature coefficients and residue-specific

34 Further, in constant temperatures, contrary to physiological expecta

35 s between 17 and 27 degrees C, relative to a constant-temperature control.

36 reserving growth of spiral steps rotating at constant temperature-dependent angular velocities around

37 ir effect on (3)J(PH), the negative coupling constant, temperature-dependent chemical shifts due to r

38 y conformation when used in conjunction with constant temperature discontinuous molecular dynamics, a

39 otein dynamics when used in conjunction with constant-temperature discontinuous molecular dynamics, a

40 iable temperature environment and not in the constant temperature environment.

41 from the Ebolavirus nucleoprotein gene in a constant-temperature environment.

42 ften much higher than those used in previous constant temperature experiments.

43 oses: (1) it increases the eluent entropy at constant temperature (for approximately 35%); (2) it inc

44 t serves to generate stable water flow under constant temperature, for the study of flow-induced prot

45 table states, and seeds short simulations at constant temperature from each of them to quantitatively

46 cells grown at 33 degrees C was measured at constant temperature, from 10 degrees to 40 degrees C, a

47 Isothermal methods, that operate at constant temperature, have emerged as promising alternat

48 At the same, constant temperature, homotrimers denature approximately

49 s mass (M) loss as a function of time (t) at constant temperature in a dynamic inert nitrogen atmosph

50 simultaneously screened and amplified at one constant temperature in one easy step.

51 that undergo self-sustained replication at a constant temperature in the absence of proteins.

52 5) ions m(-2) while simultaneously heated at constant temperatures in the range 823-1223 K.

53 t future studies report ES at a standardized constant temperature, incorporate more manipulative trea

54 that undergoes self-sustained replication at constant temperature, increasing in copy number exponent

55 rope required to half-denature the tracer at constant temperature is then estimated.

56 al effect increases with temperature and, at constant temperature, is invariant over a wide range of

57 At constant temperature, isolated nuclei behaved like passi

58 ound a single cell, our approach can produce constant temperature jumps over 50 degrees C in submilli

59 ral repressor FLC on flowering time by using constant temperature laboratory conditions.

60 Conversely, under constant temperature microwave conditions (200 degrees C

61 t better convergence is achieved compared to constant temperature molecular dynamics simulation, with

62 rmal pressure, constant surface tension, and constant temperature (NP(N)gammaT) molecular dynamics (M

63 Compared to the natural situation (NS) at a constant temperature of 10 degrees C, both UTES systems

64 ing shed for 60h using 2ppm of ethylene at a constant temperature of 20 degrees C.

65 Experiments kept at a constant temperature of 21 degrees C support the existen

66 ised forward primers on specific rings, at a constant temperature of 37 degrees C and in less than 60

67 unts of DNA copies in less than an hour at a constant temperature of 37 degrees C, achieving a limit

68 being completed in less than 15 minutes at a constant temperature of 37 degrees C.

69 lized to CO2 within 50 incubation years at a constant temperature of 5 degrees C, with vulnerability

70 tion, the simulation was run for 3.8 ns at a constant temperature of 50 degrees C and a constant pres

71 en and thermal degradation when exposed to a constant temperature of 50 degrees C, resulting in decre

72 EOP rate by more than 2-fold compared to the constant-temperature polarization rate (e.g., giving eff

73 elicited below 20 degrees C and that at any constant temperature, potentiation can be described by a

74 activity rhythm varied little when tested at constant temperatures ranging from 20 to 29 degrees C.

75 Activity within the shuttle-box under a constant temperature regime was also measured.

76 temperature dependence of Rsoil by assuming constant temperature sensitivity and linearly interpolat

77 led embryos maintained in darkness and under constant temperature show elevated non-oscillating level

78 ol maintained the desired temperature in the constant temperature simulation segments.

79 ifferent phases to coexist in equilibrium at constant temperature T and pressure P, the condition of

80 nce and works between two heat reservoirs at constant temperatures T h and T c (<T h ).

81 Our simulations were performed at constant temperature (T = 50 degrees C) and pressure (P

82 simulations leads to the conclusion that at constant temperature the size of fluid-phase domains, nf

83 At constant temperature, the rates of sulfate reduction in

84 are filled with CO2 and H2O and shaken in a constant-temperature water bath for at least 90 min.

85 s C slows parasite development compared with constant temperatures, whereas fluctuation around <21 de

86 The CPT reaction occurs at a constant temperature, which allows the probe to anneal t