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1 5 min), an excellent detection limit (a few picograms), a large linear dynamic range (>4 orders of m
2 resent work describes a method to quantitate picogram amounts of 14,15-EET enantiomers by capillary e
3 ed in this study enabled the quantitation of picogram amounts of cer-PE containing both unsaturated d
7 bined T-cell infusion, a single injection of picogram amounts of NGR-TNF, a tumor vessel-targeted TNF
9 genomic DNA, exponential amplification from picogram amounts, conversion of misincorporations to mis
10 ry mediator lipoxin A4 was detectable in low picogram amounts, using a novel fluorescence-based detec
12 ence from the chloroplasts, at approximately picogram and subcellular levels by probing inherent mole
13 Here, we utilize microfluidics to isolate picogram and subpicogram mRNA templates, as well as to s
16 2-10B4-derived PG, but not glycoproteins and picogram concentrations of recombinant human interleukin
18 separation for all PAH isomers and with low picogram detection limits on column for all analytes usi
20 s spectrometric method was developed for low-picogram detection of an ergot alkaloid, cabergoline, in
21 ion has been shown to be blocked by very low picogram doses of okadaic acid indicating that inhibitio
24 ed with limits of quantification inferior to picograms for the majority of analytes (0.05-125 pg) and
25 hocyanin cyanidin 3-glucosylrutinoside (2339 picograms/gram of tissue) was detected in bladder, follo
28 renylmethyl esters of PGF(2alpha) isomers at picogram level are complicated by numerous interfering p
29 solute quantification method and demonstrate picogram level quantification of prostate-specific antig
30 order (tertiary/quaternary) structure at the picogram level, which is undetectable using conventional
34 the potential of this approach by detecting picogram levels of a liver-specific miRNA from rat liver
45 s (given as geometric mean concentrations in picograms/milliliter) of interleukin-6 (IL-6; 485.2 vers
46 d directly via electrophoretic separation of picogram-nanogram levels of total RNA isolated from mult
48 d flagellar preparations (having less then 1 picogram of LPS/mug) was significantly reduced compared
50 NA profiles to be obtained from only tens of picograms of DNA, corresponding to a few cells, even for
52 gh levels of amplification from as low as 50 picograms of mRNA while offering a dynamic range of over
53 selective ion monitoring mode, allowing for picograms of neurosteroids to be quantified from biologi
54 idic-FCS platform is accomplished using only picograms of protein and DNA samples and less than 1 h t
56 ell line and human tissue samples containing picograms of starting material, which is an order of mag
59 e the absolute amounts of target proteins at picogram or sub-picogram levels per nanogram of cell lys
62 prevented routine quantification in the low picogram per milliliter (parts per trillion, ppt) range
64 sensitive assay for I in human plasma at low picogram per milliliter concentrations using LC/MS/MS wi
73 ents, limits of detection in the hundreds of picograms per liter for metals in solution have been obt
74 by determining amounts of MCLR down to a few picograms per liter with an automated array biosensor an
75 volunteers show a large disparity from a few picograms per milliliter (pg/ml) to several nanograms pe
76 The detection limits (3sigma) in the tens of picograms per milliliter level for the elements studied
79 demonstrate the limit of detection of a few picograms per square millimeter of surface-bound molecul
81 nalytical method to quantify the drug at low picogram-per-milliliter concentrations in biological mat
82 sterone concentrations declined to less than picograms-per-milliliter levels and remained suppressed
84 ification assay allowed the determination of picogram quantities (1.2 mug/L) of protein, and the cell
85 requires extremely small amounts of protein (picogram quantities and nanoliter volumes) and is easily
86 ical polarimetry measurements, thus allowing picogram quantities of adsorbed molecules to be characte
87 lymerase chain reaction (DOP-PCR) to amplify picogram quantities of human genomic DNA for the purpose
89 ts the generation of cDNA libraries from sub-picogram quantities of RNA robustly, efficiently and rep
90 ition of oxygenation could be determined for picogram quantities of underivatized monohydroxy fatty a
93 imits for most neurosteroids were in the low picogram range with the exception of progesterone and di
94 ode, yielding limits of detection in the low picogram range, particularly when analyzed from a glass
95 ry good sensitivity (detection limits in the picogram regime are reported for several test compounds
99 DNA down to a mass of human genomic DNA (5.5 picograms) that is roughly equal to the mass in a single
100 This system is used for the analysis of picogram to femtogram amounts of E. coli digests; for ex
105 (VI)), can be quantified down to 7.3 and 8.3 picogram total Se, respectively, in an overall analytica
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