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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
14                                     By using heparin-Sepharose affinity to discriminate between the m
15 ded its cell culture host range and bound to heparin-Sepharose, although it did not require cell surf
16                                        Using heparin-Sepharose and DNA-specific columns, we partially
17 tracts using ammonium sulfate fractionation, heparin-Sepharose and Mono Q chromatography, and BTE-aff
18 fied 5000-fold from PE-treated TFG2 cells by heparin-Sepharose and RNA affinity chromatography.
19  well, decrease both the affinity of Ang for heparin-Sepharose and the capacity of Ang to support cel
20 ty by chromatography through DEAE Sepharose, Heparin Sepharose, and phosphocellulose columns.
21 ,000-fold from rat livers by DEAE-Sepharose, heparin-Sepharose, and DNA affinity chromatography.
22 beled active fractions from the Q-Sepharose, heparin-Sepharose, and WGA-agarose also indicated only t
23 by sequential chromatography on Q-Sepharose, heparin-Sepharose, and WGA-agarose.
24                      Mutant K45A eluted from heparin-Sepharose at lower NaCl concentrations than wild
25 65 and VEGF121 showed increased retention on heparin-Sepharose at pH 5.5 compared with pH 7.5.
26 nhanced activities, but they all eluted from heparin-Sepharose at significantly higher ionic strength
27                     Dose-response curves and heparin-Sepharose binding suggested Ad.hFX has greater a
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
30                                              Heparin-Sepharose chromatography demonstrated that HL-LP
31         The second peak of activity from the heparin-Sepharose chromatography represented a purificat
32                      Further purification by heparin-Sepharose chromatography resulted in separation
33 ted laminin-1 fragments were fractionated by heparin-Sepharose chromatography.
34 , Sephadex G-75, concanavalin A-agarose, and heparin-Sepharose chromatography.
35 ly purified from four edema-fluid samples by heparin-Sepharose chromatography.
36  Chinese hamster ovary cells and purified by heparin-Sepharose chromatography.
37  agarose affinity chromatography followed by heparin-sepharose chromatography.
38 le for complexes IIa and IIb (TeRF II) using heparin-Sepharose chromatography.
39 us ST132 and purified to near homogeneity by heparin Sepharose CL-6B affinity chromatography.
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
42                                              Heparin-Sepharose column chromatography and analytical u
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
46  chromatographic steps, including 2 steps of heparin-Sepharose column, is reported.
47  and FGF-2 isoforms were further purified by heparin-Sepharose column.
48                        In this study we used heparin-Sepharose columns to demonstrate that PVC-211 Mu
49  reduced virulence in cattle and can bind to heparin-Sepharose columns, and vCRM8, which is highly vi
50                                        Using heparin-Sepharose-enriched fractions that hybridized to
51                          Western blotting of heparin-Sepharose-enriched supernatant mainly detected t
52                    Binding experiments using heparin-Sepharose gel demonstrated that the lipid-free 1
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
57 ent elution profiles of APC derivatives from Heparin-Sepharose supported this conclusion.
58                           TE bound better to heparin-Sepharose than 633, but this difference was not
59                                              Heparin-Sepharose was used to characterize heparin-GST-L
60 nalysis of GH3 nuclear proteins that bind to heparin-Sepharose, we have shown that Ets-1 and GABP, wh
61                                        Using heparin-Sepharose, we isolated two of the protein forms
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
64                Wild-type MIP-1alpha bound to heparin-Sepharose, while three of the mutants, R18A, R46
65  The GST-VEGF-exon 7 fusion protein bound to heparin-Sepharose with a similar affinity as VEGF165 and
66             Moreover, these mutants bound to heparin-Sepharose with lower affinities.
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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