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1 ven in the presence of salt) followed by EAH-Sepharose chromatography.
2 ied from four edema-fluid samples by heparin-Sepharose chromatography.
3 hamster ovary cells and purified by heparin-Sepharose chromatography.
4 ells by ammonium sulfate precipitation and Q-Sepharose chromatography.
5 affinity chromatography followed by heparin-sepharose chromatography.
6 nin-1 fragments were fractionated by heparin-Sepharose chromatography.
7 omplexes IIa and IIb (TeRF II) using heparin-Sepharose chromatography.
8 ffinity purified from cell lysates by Ni(2+)-Sepharose chromatography.
9 ionic detergent and purified further by DEAE-Sepharose chromatography.
10 acts of acetone-grown R. rhodochrous by DEAE-Sepharose chromatography.
11 artially purified by hydroxyapatite and blue Sepharose chromatography.
12 ex G-75, concanavalin A-agarose, and heparin-Sepharose chromatography.
13 pH 7.5), and hydrophobic interaction (phenyl-Sepharose) chromatographies.
14 the N- terminal domains purified by m(7)GTP-Sepharose chromatography and polyacrylamide gel electrop
15 rom the active supernatant by concanavalin A Sepharose chromatography and separated by sodium dodecyl
16 in the separation of two fractions by phenyl-Sepharose chromatography, both of which phosphorylated a
17 olated from plasma of the proband by heparin-Sepharose chromatography contained amounts of beta antit
19 neutrophils is shown to be resolved by DEAE-Sepharose chromatography into two fractions: an NADPH-cy
20 We report that crosslinked agarose (e.g., Sepharose) chromatography medium that has been chemicall
21 a Ca(2+)-dependent manner as measured by CaM-Sepharose chromatography or a dansyl-CaM fluorescence as
22 The second peak of activity from the heparin-Sepharose chromatography represented a purification of 1
24 eparated and present in "fraction 42" from Q-Sepharose chromatography specifically phosphorylated GRP
25 protein and was purified using methotrexate-Sepharose chromatography to yield 10 mg of homogeneous D
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