ライフサイエンスコーパス: nanomole

1 cidation of new molecules down to only a few nanomole.

2 pecific biomolecules at the level of tens of nanomoles.

3 ration increased from 32.92 before to 111.72 nanomoles/4 mm per hour after removal of the RPE.

4 ransport rates increased from 0.158 to 0.439 nanomoles/4 mm per hour after removal of the RPE.

5 at bind to the HIV-1(BaL) gp120 protein with nanomole affinity were isolated from a RNA library by th

6 rolling-circle amplification, that produces nanomole amounts of single-stranded oligonucleotides per

7 t of S-nitroso compound levels from pico- to nanomole amounts.

8 staglandin I2 receptors (IPs); Kb values (in nanomoles) are given in parentheses.

9 low as a few picomoles to as high as several nanomoles can be determined in a microtiter plate in 10-

10 onstant was 1.9 mM, the maximum flux was 8.9 nanomoles/cm2 per hour, and the apparent Na+ :L-lactate

11 asurements are shown to be feasible even for nanomole concentrations of a membrane-associated peptide

12 ma, expressed as relative mole percent or as nanomoles fatty acid per milliliter of plasma.

13 d for donors younger than 30 age and 18+/-11 nanomoles/g dry choroid for donors older than 80.

14 trations of CoQ10 in the choroid was 27+/-16 nanomoles/g dry choroid for donors younger than 30 age a

15 ors younger than 30 years of age and 24+/-13 nanomoles/g dry retina for donors older than 80 years of

16 entration of CoQ10 in the retina was 42+/-11 nanomoles/g dry retina for donors younger than 30 years

17 s was not seen until NO3- was detectable (30 nanomoles/gram fresh weight) in the leaves.

18 le of large and very fast pressure drops (<1 nanomole, >2,500 atmospheres and <0.7 microseconds).

19 on was dose dependent, with injections of 10 nanomoles having virtually no effect to a maximum loss o

20 uantitating isothiocyanates (R-N=C=S) at the nanomole level is based on the observation that the high

21 m) of 73 +/- 9 microM, V(max) of 2.0 +/- 0.1 nanomoles/min per milligram protein, and K(d) of 0.44 +/

22 = 33 +/- 8 microM and V(max) = 0.26 +/- 0.03 nanomoles/min per square centimeter), energy independent

23 a potential diagnostic dose (25 mg/kg or 455 nanomoles Mn(2+)/kg; ~2 orders of magnitude lower than t

24 the GCL within 6 days after injection of 160 nanomoles NMDA.

25 sured as the log of histidine revertants per nanomole of amine, log m, in Salmonella typhimurium TA 9

26 Tissue concentrations (nanomole of chains per mg dry weight) of all glycosamino

27 hat 1.5 x 10(8) SAR11 cells are produced per nanomole of DMSP.

28 From one printing run that consumes <1 nanomole of each compound, large combinatorial libraries

29 to analysis by this method using less than a nanomole of material.

30 The activities expressed per nanomole of P450 in insect microsomes were similar for P

31 ins up to 120 nmol of Triton X-100 bound per nanomole of the enzyme.

32 Fifty nanomoles of 4a blocked only 30% of the specific binding

33 per square centimeter) and oxidized 33 to 45 nanomoles of ascorbate over 1 hour in the absence of oxy

34 lid-state NMR spectra for several to tens of nanomoles of beta-amyloid fibrils and ubiquitin in 1-2 d

35 phic peaks 15 s wide and containing up to 30 nanomoles of carbon was quantitatively converted to CO2

36 nts on samples containing as little as eight nanomoles of GB1.

37 Fifty nanomoles of NMDA were injected in the sensorimotor cort

38 ively detected at micromolar concentrations (nanomoles of target) using resistive pulse sensing, conf

39 of less abundant phenolic conjugates down to nanomoles of trapped amounts of metabolite corresponding

40 Nanomoles of VOC can be detected with the VAHIIA system,

41 cific activity (SA, in counts per minute per nanomole) of serum all-trans ((3)H)retinol in all mice e

42 roM lysozyme solution corresponds to only 13 nanomoles or 1.9 microg of lysozyme.

43 d oocytes (0.48+/-0.03 versus 0.016+/-0.005 (nanomoles per hour(-1) per oocyte, respectively).

44 esters in the shoots was determined to be 74 nanomoles per kilogram fresh weight as measured by isoto

45 ose (in millimoles per liter), C-peptide (in nanomoles per liter), hemoglobin A1c (as a percentage) a

46 deficient, less than 12 ng/mL (to convert to nanomoles per liter, multiply by 2.496); insufficient, 1

47 ] ng/mL vs 13.86 [5.49] ng/mL [to convert to nanomoles per liter, multiply by 2.496]).

48 5 [0.43] mug/dL, respectively [to convert to nanomoles per liter, multiply by 27.588]; beta = 0.18; P

49 , 12.3 mug/dL to 16.5 mug/dL) (to convert to nanomoles per liter, multiply by 29.6); 20.7 mug/dL for

50 s of 15.00 microg/L or higher (to convert to nanomoles per liter, multiply by 5.675) were assumed to

51 The PuO(2) + H(2)O reaction rate is 0.27 nanomoles per meter squared per hour at 25 degrees C; th

52 ecific activity was approximately 600 to 700 nanomoles per milligram protein per minute, and the late

53 scently labeled peptides are on the order of nanomoles per millimeter of length of monolith material

54 ranging from low picomoles per mol (ppt) to nanomoles per mol (ppb), depending on location and compo

55 It accumulates to a level of 4.8 nanomoles per plant in the kernel, more than 10 times th

56 o)resorcinol assay of Hunt et al. to measure nanomole quantities of Co(2+), Ni(2+), and Cu(2+) as wel

57 Accumulation of nanomole quantities of collected and recovered material

58 Incubation produces nanomole quantities of enzymatic products per a blood sp

59 m to the formazan enables the measurement of nanomole quantities of glyoxylate in an assay that is am

60 ne NMR detection to separate and concentrate nanomole quantities of heparin oligosaccharides.

61 )) by Fura-2 and can also be used to measure nanomole quantities of these ions.

62 le volumes less than 5 microliter containing nanomole quantities or less of impurities.

63 H NMR spectra can be acquired for microgram (nanomole) quantities of trace impurities in a complex sa

64 e quantities with linear responses up to the nanomole quantity range.

65 ed for concentrations in the low picomole to nanomole range, with correlation coefficients of R(2) >

66 F-MS method fell within the high-picomole to nanomole range.

67 d with a rapid and quantitative assay in the nanomole range.

68 CRF receptors in the high picomolar and low nanomole ranges, respectively.

69 n (CEC) method to determine configuration on nanomole scale.

70 eld of 2',5'-branched RNA on the preparative nanomole scale.

71 identify (13)C NMR signals in samples at the nanomole-scale that arise from Cl-substituted (13)C by e

72 le to detect complementary target DNA in sub-nanomole scales.

73 imate amounts of acid or alkali secretion in nanomoles secreted per minute.

74 ree systems, 100 microM 22:6OOH induced 74.7 nanomoles superoxide per milligram plasma membrane prote

75 :6OOH-activated PMNs produced 11.10 +/- 0.68 nanomoles superoxide, and production was suppressed 72%

76 ns, fMLP induced production of 34.6 +/- 2.77 nanomoles superoxide, and RPP inhibited 60% of productio

77 exes present in quantities as small as a few nanomoles (tens of micrograms for the observed component

78 eported methods (typically around US$ 20 per nanomole total oligonucleotides produced) and is dominat