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1 fibrinogen by ion-exchange chromatography on DEAE-cellulose.
2 ygalacturonase, followed by fractionation on DEAE-cellulose.
3 edure and then by stepwise chromatography on DEAE-cellulose.
4 ne anion exchanging resin-diethylaminoethyl (DEAE) -cellulose.
5 ased on absorption of the acidic proteins on DEAE-cellulose and gel filtration through agarose.
6 nt extraction, followed by chromatography on DEAE-cellulose, C18 reverse phase resin, and silicic aci
7 ort here an improved chromatographic method (DEAE-cellulose, calcium hydroxylapatite, and Sephadex G-
8                                              DEAE-cellulose chromatography and gel mobility shift ass
9 p60 from a heat-treated neutrophil lysate by DEAE-cellulose chromatography and SDS-polyacrylamide gel
10                                              DEAE-cellulose chromatography performed in a boric acid-
11                                   Similarly, DEAE-cellulose chromatography showed slightly stronger b
12 MTF was separated from uncross-linked MTF by DEAE-cellulose chromatography, and the tRNA in the cross
13  chloroform/methanol extraction, followed by DEAE-cellulose chromatography, mild alkaline hydrolysis,
14 ng glutathione-agarose, Sephacryl S-200, and DEAE-cellulose chromatography.
15 utes independently from peak 2 fibrinogen on DEAE-cellulose chromatography.
16 ted a persistent, autonomously active PKC by DEAE-cellulose column chromatography from hippocampal sl
17  apparent homogeneity using a combination of DEAE-cellulose column chromatography, ammonium sulfate p
18     These N-acyl-PS species were enriched by DEAE-cellulose column chromatography, and they were then
19                     The separation of PD, by DEAE-cellulose column chromatography, yielded two pectic
20 , and the resulting extract was subjected to DEAE-cellulose column chromatography.
21  to mild base hydrolysis and was purified by DEAE-cellulose column chromatography.
22 tent retention of nucleotides in the case of DEAE cellulose filter papers.
23 has been purified to apparent homogeneity by DEAE-cellulose, heparin-agarose, and DNA-specific affini
24 fold) from insect cells by chromatography on DEAE-cellulose, phosphocellulose, heparin-agarose, and s
25 rnatant was then efficiently adsorbed over a DEAE cellulose-treated paper wick assembled in the syrin