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1 nventional TIMS involving Pu purification by anion exchange resin.
2 preconcentrated on a minicolumn packed with anion exchange resin.
3 ng chromatography on lysine-Sepharose and an anion exchange resin.
4 into the mesoionic title compounds using an anion exchange resin.
5 in/peptide bioadsorbents to those of LayneRT anion exchange resin.
6 ped flow-cell system utilizing scintillating anion-exchange resin.
7 he water sample and the concentration on the anion-exchange resin.
8 gnificantly with pertechnetate uptake on the anion-exchange resin.
9 on of neutral to basic peptides by the added anion-exchange resin.
10 ion chromatography on AG1-X8 strongly basic anion-exchange resin.
11 eters were determined for five commonly used anion exchange resins.
12 tter than commercially available strong base anion exchange resins.
13 tion in a packed bed of amine-functionalized anion exchange resins (AERs) with a pH swing regeneratio
16 he samples by ion exchange chromatography on anion exchange resin AG 1-X4 with NH4NO3 and measured by
17 loys a commercial pipette tip packed with an anion-exchange resin and comprises four primary steps: t
18 ists of a packed bed containing a mixture of anion-exchange resin and scintillating plastic beads.
19 for 5 min with a 20% (w/v) suspension of an anion-exchange resin and sterilely filtered into a seale
20 tatively isolated from plasma via the use of anion-exchange resins and then detected and quantified i
23 his study examined removal of anionic OCs by anion exchange resins (AXRs) as a promising alternative.
24 l approximately 760 microm diameter AG 1 x 4 anion-exchange resin beads were determined using acousti
25 cation of large amounts of nucleotides using anion-exchanging resin but has shown the promise of enri
26 for the pretreatment and appropriate use of anion exchange resins by drinking water utilities and fo
28 g large volumes of water through cation- and anion-exchange resin columns in the field to collect sod
31 esin, PPL- and C18 - SPE cartridges, and one anion exchanging resin-diethylaminoethyl (DEAE) -cellulo
33 )Lmol(-1)cm(-1)), fixed on a Dowex 1-X8 type anion-exchange resin for 10mL, 100mL, 500mL, and 1000mL,
34 In bench-scale batch and column experiments, anion exchange resins from a large, representative group
36 underivatized monosaccharides on pellicular anion-exchange resin (HPAE) using pulsed amperometric de
37 (in a 1- to 2-ml sample) was bound to 15 mg anion-exchange resin, interfering ions were removed in a
39 nd quenched (131)I by 5 min of stirring with anion-exchange resin renders a multi-gigabecquerel-level
40 this research was to develop a scintillating anion exchange resin selective for monitoring (129)I at
41 an appropriate mixture of self-regenerating anion exchange resins that selectively remove and replac
42 riately designing or tuning the mixed bed of anion exchange resins, the process can be extended to ne
43 ydrates can be separated by using Dowex 1-X8 anion exchange resin, this method can be used specifical
44 s added to anoxic extractions using a strong anion exchange resin to separate dissolved U(IV) and U(V
49 The protein demonstrates little affinity for anion exchange resins, with contaminating proteins remov