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1 he flow-through fraction upon subsequent ATP-agarose chromatography.
2 s, was purified using anion exchange and red-agarose chromatography.
3 um sulfate precipitation followed by heparin agarose chromatography.
4 te precipitation, octyl agarose, and heparin agarose chromatography.
5 antithrombin that are resolvable by heparin-agarose chromatography.
6 s separable from the PLD activity by heparin-agarose chromatography.
7 ins (particularly RNase MRP) by streptavidin agarose chromatography and could be recovered by the elu
9 of delta helicase from pol delta on heparin-agarose chromatography and its purification to apparent
10 ed from murine serum by gelatin cross-linked agarose chromatography and subsequently was enzymaticall
11 polymerase was partially purified by heparin-agarose chromatography and used in conjunction with a pl
12 were purified to near homogeneity by Ni(2+)-agarose chromatography and were shown to be highly activ
14 ellulose chromatography, unique-sequence RNA-agarose chromatography, and ceramic hydroxyapatite chrom
15 e-tagged carboxy-terminus was purified by Ni-agarose chromatography, and this variant was used to dem
16 arrying maleimido-butyryl-biocytin by avidin-agarose chromatography; and (v) identification of the is
19 ation of GCS was achieved via a two-step dye-agarose chromatography procedure using UDP-Glc to elute
20 f (His6)BglK by nickel-nitrilotriacetic acid-agarose chromatography provided high purity enzyme in qu
22 Fluorescence quenching and reactive blue agarose chromatography studies revealed that it binds to
23 ysophosphatidyl glycerol (LPG) by Ni(2+)-NTA agarose chromatography to >95% purity with high yield.
24 in N. crassa, we used methyl-binding-domain agarose chromatography to isolate the methylated compone
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