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