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