戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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
8  by ammonium-sulphate precipitation, heparin-agarose chromatography and gel filtration.
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
13         Using amino-terminal sequencing, ATP-agarose chromatography, and a carboxyl-terminal-specific
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
17 d with selective retentivity onto a Ni2+-NTA-agarose chromatography matrix.
18                          However, by heparin-agarose chromatography of high-salt extracts of human sk
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
21                                 Streptavidin-agarose chromatography studies have indicated that gluta
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

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。