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1 peptides encompassing 2 of 5 motifs bound to heparin-Sepharose.
2 raphy on Ni-NTA-agarose, DEAE-Toyopearl, and heparin-Sepharose.
3 mutants lost their affinities for binding to heparin-Sepharose.
4 ombinant protein on spin columns packed with heparin-sepharose.
5 ntration of NaCl required to elute FXIa from heparin-Sepharose.
6 highly virulent in cattle and cannot bind to heparin-Sepharose.
7 , heating, trypsin digestion, and binding to heparin-Sepharose.
8 ts adhesion, and Ang itself binds tightly to heparin-Sepharose.
9 BP-3) into six fragments, four of which bind heparin-Sepharose.
10 PECAM-1 failed to interact specifically with heparin-Sepharose, 3H-labeled heparin, or a heparin-bovi
11 When XO was bound to a prototypical GAG, heparin-Sepharose 6B (HS6B-XO), the rate of inactivation
12 c mice, VLDL from HuCI transgenic mice bound heparin-Sepharose, a model for cell-surface glycosaminog
13 ydrophobic interaction, lectin affinity, and heparin Sepharose affinity chromatography followed by SD
15 ded its cell culture host range and bound to heparin-Sepharose, although it did not require cell surf
17 tracts using ammonium sulfate fractionation, heparin-Sepharose and Mono Q chromatography, and BTE-aff
19 well, decrease both the affinity of Ang for heparin-Sepharose and the capacity of Ang to support cel
22 beled active fractions from the Q-Sepharose, heparin-Sepharose, and WGA-agarose also indicated only t
26 nhanced activities, but they all eluted from heparin-Sepharose at significantly higher ionic strength
28 re purified sequentially with DEAE-Sephacel, heparin-Sepharose, ceramic hydroxyapatite, Mono Q, pheny
29 ombin isolated from plasma of the proband by heparin-Sepharose chromatography contained amounts of be
40 quential DEAE-Sephacel, phenyl-Sepharose FF, heparin-Sepharose CL-6B, and Q-Sepharose FF column chrom
41 inoglycan binding, MIP-1beta-A10C binds to a heparin-Sepharose column as tightly as the wild type pro
43 ells, was used to monitor purification after heparin-Sepharose column chromatography, Mono-S, and C4
44 the mutants, but not of the wild type, to a heparin-Sepharose column produced binding comparable to
45 n of extracts of ammonium-grown cells with a heparin-Sepharose column resolved them into a fraction e
49 reduced virulence in cattle and can bind to heparin-Sepharose columns, and vCRM8, which is highly vi
53 atography on Ultrogel AcA 34, DEAE-Sephacel, heparin-Sepharose, hydroxylapatite, and Ultrogel AcA 44.
54 duced has been purified using, successively, heparin-Sepharose, Mono Q, and Mono S FPLC (fast protein
55 tations did not alter either HCII binding to heparin-Sepharose or HCII inhibition of thrombin in the
56 ion markedly, but DS displaced thrombin from heparin-Sepharose, suggesting that DS and heparin share
60 nalysis of GH3 nuclear proteins that bind to heparin-Sepharose, we have shown that Ets-1 and GABP, wh
62 the wild type recombinant fragment bound to heparin-Sepharose, where it was eluted at the same NaCl
63 from oocytes and eggs via chromatography on heparin-Sepharose, whereas we isolated chromatinized his
65 The GST-VEGF-exon 7 fusion protein bound to heparin-Sepharose with a similar affinity as VEGF165 and
67 ed heparin binding could be dissociated from heparin-Sepharose with much lower NaCl concentrations, i
68 omogeneity by sequential chromatography over heparin-sepharose, xanthine amino congener-agarose, and
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