ライフサイエンスコーパス: coelution

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1 by 1D GC/MS and may be overestimated, due to coelution.

2 eak capacity lowering the occurrence of peak coelutions.

3 he synthetic nucleoside adduct included HPLC coelution and identical spectral properties with a natur

4 Vacuum UV detection was necessary to solve a coelution between saturates and monoaromatics.

5 o GC-VUV data sets is that a large number of coelution events can be tolerated, resulting in signific

6 mpared to SWATH was investigated in a forced coelution experiment (up to 20 analytes coeluting).

7 cterial two-hybrid analysis and confirmatory coelution experiments that PhoU interacts with PhoR thro

8 cts i.e., column overload and matrix-analyte coelution for a variety of LCn/MSn applications.

9 precipitation followed by mass spectrometry, coelution from a gel filtration column, cosedimentation

10 amples, and thus reducing the possibility of coelutions; (III) to eliminate the essential-oil "matrix

11 Component coelution in chromatographic analysis complicates identi

12 ectivity to differentiate PASH from PAH when coelution occurred.

13 has not been possible due to chromatographic coelution of alkenones with the same carbon chain length

14 These results were also supported by the coelution of CAPP with trimeric and dimeric PP2A on size

15 oiding the addition of competitor ligands or coelution of common contaminants.

16 y, sensitivity, and resolution, plus precise coelution of deuterated and nondeuterated EETs.

17 gnificantly different deltaD values and that coelution of different alkenones may lead to erroneous s

18 be severely impeded by close chromatographic coelution of distinct metabolites.

19 assigned to NM23-H1 by virtue of: 1) precise coelution of enzymatic activity with wild-type and mutan

20 Coelution of HDL with plasma proteins such as albumin oc

21 (ii) Coelution of HisG and HisZ during affinity chromatograph

22 fused-core C18 column, thereby avoiding the coelution of main ellagitannins, such as vescalagin and

23 raphy, and total synthesis, and confirmed by coelution of native and synthetic APF derivatives on mic

24 Coelution of organic compounds that do not contain S can

25 Western blotting showed coelution of PM20D2 with beta-alanyl-lysine dipeptidase

26 ue to the formation of unstable derivatives, coelution of similar compounds, long sample collection t

27 he isolated acid was determined to be (R) by coelution on HPLC of its derivative with Marfey's reagen

28 lumn overload, (ii) matrix component-analyte coelution, or a combination of each.

29 , interference due to isotopic impurities or coelution was not encountered.

30 e identity of the 3-NT peak was confirmed by coelution with authentic standards and by the in vitro p

31 bisnorbiotin methyl ketone, respectively, by coelution with authentic standards on HPLC.

32 Peaks were identified by coelution with known standards.

33 f these 12 compounds, as they showed partial coelution with other components in the first chromatogra

34 oreactivity in these tissues was verified by coelution with synthetic PACAP in reverse-phase HPLC ana

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