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1  with a lower limit of quantification of 0.1 picomoles.
2  for components on the level of sub-10 ng or picomole (1 pmol).
3 in very small amounts, in the order of a few picomoles/10(9) APC.
4  profiling of digest aliquots containing low picomole amounts of carbohydrate structures either enzym
5                                          Low picomole amounts of CEP-HSA and CEP-dipeptide stimulated
6 ctrometry (LC-ESI-MS) to detect femtomole to picomole amounts of reporter molecules results in an ult
7 ionic liquid matrices allow the detection of picomole amounts of the sodium salts of a disaccharide,
8  been possible to rapidly sequence femto- to picomole amounts of tissue-derived complex polysaccharid
9 en EDTA was present and could be detected in picomole amounts.
10 ating their function can be studied with sub-picomole cGMP sensitivity.
11 y (R(2) > 0.9996), resolution (R(s) 1.5) and picomole detection limits, and was successfully applied
12 R(2) > 0.9996), resolution (R(s) >= 1.5) and picomole detection limits, and was successfully applied
13     This allowed better performances for the picomole detection of low mass analytes like arginine, f
14                      Sensitive detection (<1 picomole Fe) is achieved using an iron-free HPLC system
15  analyte loadings ranging from femtomoles to picomoles for metabolites.
16 nescent ions, accumulation of some femto- to picomoles in a neon matrix (over a time scale of tens of
17 limit of detection (10-fold enhancement, 100 picomole) in the detection of angiotensin II.
18 mbinant human VEGF165 for 20 minutes (80-450 picomoles/kg body weight).
19 trate that small hydrophilic peptides at the picomole level can be desalted and characterized by matr
20 e level in solution-phase digests and at the picomole level in digests of samples separated on SDS-PA
21 method for the analysis of delta(34)S at the picomole level in individual compounds.
22 ligosaccharides are detected at only the low picomole level with DHB, alternative matrices were scree
23                        Moreover, even at the picomole level, there are enough sequence ions in the ma
24             Mixtures of peptides, at the low-picomole level, were analyzed by liquid chromatography a
25 reparation for microsequence analysis at low picomole level.
26 in glycosylation by mass spectrometry at the picomole level.
27 -trypsin and IgG-protein G complexes, at the picomole level.
28 dansylation are resolved and detected at sub-picomole levels by reversed-phase HPLC.
29 e ADHP-neoglycolipids are well retained, and picomole levels can be detected using monoclonal carbohy
30 a 2M and beta 2M-AGEs can be detected at low picomole levels directly in bovine serum.
31  full-scan electrospray mass spectra for low-picomole levels of cytochrome c contained in a 1536-well
32 obicity, enhanced ionization efficiency, and picomole levels of detection limits.
33                           The release of sub-picomole levels of N-linked oligosaccharides directly fr
34 ration range and can accurately quantify sub-picomole levels of released glycans, providing a needed
35 ort chain thioesters and is sensitive to sub-picomole levels of these compounds.
36 n PNA purity and sequence information at low picomole levels will be important as greater quality con
37 ntification of catechins at femtomole to low-picomole levels without extraction or sample pretreatmen
38 ed by analysis of the associated tags at sub-picomole levels.
39  (CD) have pushed the limits of detection to picomole levels.
40 inguished from common PTH amino acids at low picomole levels.
41    Basal [(3)H]cAMP content was 13.4 +/- 1.3 picomoles/mg protein (SEM).
42        Rho-123 uptake in SIRC cells was 14.4 picomoles/mg protein and in the presence of CsA (10 micr
43 in the presence of CsA (10 micro M) was 70.8 picomoles/mg protein at 3 hours.
44  rabbit lacrimal gland at a rate of 14 +/- 7 picomoles/mg protein per minute.
45 tein was detected at a concentration of 44.6 picomoles/mg protein, along with its redox partner NADPH
46 ccumulation to 23.2 +/- 4.4 and 31.6 +/- 4.6 picomoles/mg protein, respectively.
47 cumulation to 36.0 +/- 3.9 and 73.2 +/- 17.5 picomoles/mg protein, respectively.
48 -21 femtomoles/mg protein and 4.3 nM and 1.3 picomoles/mg protein, respectively.
49  a receptor concentration of approximately 3 picomoles/mg protein.
50 s REH activity in P2 were 18 microM and 1800 picomoles/min per mg, respectively.
51 GSH+/-acivicin (17.7+/-4.3 versus 15.7+/-1.4 picomoles/min(-1) per 10(6) cells).
52 taining medium (10.3+/-0.7 versus 16.8+/-0.9 picomoles/min(-1) per 10(6) cells; P < 0.01).
53 vity of 1.6x10(3) counts.sec(-1).muW(-1) per picomole of Cy7.
54  obtained at 30 microM, corresponding to one picomole of protein.
55 s determined to be 53 +/- 2 pmol adenine per picomole of ricin per hour.
56                                          Ten picomoles of 3-O-(pentafluorobenzyl)-alpha-estradiol wer
57 ay format, limits of detection down to a few picomoles of and excellent specificity for each dNTP aga
58 ar assembly yet examined; second, only a few picomoles of Arp2/3 was required for individual experime
59  polypeptides in a mixture, using only a few picomoles of each substrate and physiological amounts of
60                                        A few picomoles of heparin-derived, sulfated hexa- to decasacc
61                    Detectability was down to picomoles of hydrogen peroxide (4 pmol for CL and 210 pm
62 ivity of detection has been lowered to a few picomoles of isothiocyanate.
63                                 Four hundred picomoles of norbenzphetamine and 21 pmol of cyclohexano
64 ed and activated (564+/-73 versus 1021+/-141 picomoles of PO(4); P=0.015) by PDGF.
65                                         Only picomoles of protein are required for each reaction, whi
66 Thus, MAbs selectively identify and quantify picomoles of remaining protecting groups on antisense th
67                                   Since only picomoles of salt are needed to generate bubbles, pH gra
68 urate detection and quantification using sub-picomoles of sample.
69 re calmodulin assay to be performed with 200 picomoles of solute.
70 attice relaxation, allowing the detection of picomoles of substance.
71 nsitivity, with the capability to detect few picomoles of target DNA.
72  or fluorescence that are sensitive to a few picomoles of target.
73 homotetramer protein, in free solution using picomoles of the protein.
74                                              Picomole or less amounts of protein reagent are consumed
75 ipheral blood mononuclear cells (median 0.16 picomole per 10(6) cells) for more than 20 months.
76 r hour of indole-3-acetyl-myo-inositol and 1 picomole per plant per hour of indole-3-acetic acid to t
77 onth-old normal and VPP mice were 425 +/- 90 picomoles per eye and 115 +/- 33 picomoles per eye, resp
78  425 +/- 90 picomoles per eye and 115 +/- 33 picomoles per eye, respectively (mean +/- SD).
79 rm tissues have enzyme activities of 1 to 10 picomoles per hour per milligram protein.
80 al and hepatic sinusoidal insulin levels (in picomoles per liter) during the experimental period were
81 ontrols (median, 18.8 muIU/mL [to convert to picomoles per liter, multiply by 6.945]) and maternal sa
82 asting insulin (-2.75 muIU/mL [to convert to picomoles per liter, multiply by 6.945]; 95% CI, -4.50 t
83 94 muIU/mL; 95% CI, 1.28-2.61 [to convert to picomoles per liter, multiply by 6]; P < .001), glycated
84 a maximum uptake rate (Vmax) of 22.0 +/- 1.0 picomoles per milligram protein per minute.
85 the atlas to represent protein densities (in picomoles per milliliter).
86  amounts in the range of tens to hundreds of picomoles per million cells.
87 it has a high specific activity of about 100 picomoles per minute per microgram in the presence of Ca
88  atmospheric mole fractions ranging from low picomoles per mol (ppt) to nanomoles per mol (ppb), depe
89 ution to ascertain the stability of the 2008 picomoles per mol NMHC standards suite.
90  Technology (NIST) developed and reported on picomoles per mol standards containing 18 nonmethane hyd
91 ounds covering the mole fraction range of 60 picomoles per mol to 230 picomoles per mol.
92 raction range of 60 picomoles per mol to 230 picomoles per mol.
93 alactoside in the endosperm supplies about 2 picomoles per plant per hour of indole-3-acetyl-myo-inos
94 e-3-acetic acid and indole-3-acetic acid (62 picomoles per shoot).
95 face DMHg and the highest DMHg evasion (~9.4 picomoles per square meter per hour) found in upwelling
96  in burned animals at 7 days (125.4 +/- 15.5 picomoles [pmol]; p = .01) and at 14 days (216.7 +/- 50.
97 is fast (a few minutes) and operates best on picomole quantities of analyte in sample volumes less th
98 y, RT is a nanoscale technique utilizing sub-picomole quantities of analyte.
99 sults support the possibility of identifying picomole quantities of crosslinked peptides by similar s
100 ase HPLC techniques expedite the analysis of picomole quantities of dityrosine.
101 hod provides an accurate characterization of picomole quantities of DNA-protein complexes.
102 experimental constraints to rapidly sequence picomole quantities of HLGAG oligosaccharides.
103 tabilities rapidly and accurately using only picomole quantities of material and readily accessible l
104 id chromatography (HPLC) assay for measuring picomole quantities of nitrosothiol in biological sample
105 tly reported a simple procedure by which low picomole quantities of peptides can be modified to the c
106          The performance of systems in which picomole quantities of sample are mixed with a carrier g
107 lows the quantification of precursors at low picomole quantities with linear responses up to the nano
108 o allow analysis of biomolecules at nano- or picomole quantities, reducing the required amount of mat
109 osylation was directly identified in the low picomole range by collision-induced dissociation (CID) o
110 HLA)/peptide combinations in the nanomole to picomole range with minimal run time, reconciling the sy
111  with improved signal-to-noise ratio (in the picomole range).
112 tection and quantification, resulting in the picomole range, and sensitivity as well was not signific
113 ytical sensitivities in the femtomole to low picomole range.
114  nmol), and the detection limits were in the picomole range.
115 pharmaceuticals is conducted at the nano- to picomole scale, conventional chemical characterization t
116 efficiency, as reactions can be performed on picomole scale.
117  a valuable platform for the ultrasensitive, picomole-scale screening of small-molecule drugs against
118                        Herein, we describe a picomole-scale, real-time photoreaction screening platfo
119   We show that high-resolution NMR can reach picomole sensitivity for micromolar concentrations of an
120       The detection of mir21 was achieved in picomole sensitivity through the changes of intrinsic p1
121 d fMLP, respectively, was also detectable at picomole sensitivity.
122  between log ion intensity and quantity from picomole to femtomole amounts by liquid chromatography-e
123 were generated for concentrations in the low picomole to nanomole range, with correlation coefficient
124  DESI/IMS/ToF-MS method fell within the high-picomole to nanomole range.
125                    EDTA from as low as a few picomoles to as high as several nanomoles can be determi

 
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