ライフサイエンスコーパス: Southwestern blot

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1 electrophoretic mobility shift assays or on Southwestern blots.

2 ate factor is a 90-kDa protein identified in Southwestern blots.

3 detected in P. infestans nuclear extracts by southwestern blotting.

4 by electrophoretic mobility shift assays and Southwestern blotting.

5 Comparative band shift and Southwestern blot analyses conducted with cellular p46,

6 UV cross-linking and Southwestern blot analyses indicate that the IUR oligonu

7 rophoretic mobility-shift assays and Western/Southwestern blot analyses indicated that this suppressi

8 ng electrophoretic mobility shift assays and Southwestern blot analyses with a double-stranded oligon

9 binds the RBF DNA element as demonstrated by southwestern blot analyses, and by competition EMSAs bet

10 Southwestern blotting analyses and gel shift assays with

11 Two-dimensional UV cross-linking and shift Southwestern blotting analyses detected two proteins (50

12 Band shift assays, UV cross-linking, and Southwestern blot analysis confirm that the silencer ele

13 In addition, Southwestern blot analysis detected binding of the most

14 UV cross-linking and Southwestern blot analysis identified FP1-binding factor

15 Protein-DNA interactions were assessed by Southwestern blot analysis in which sodium dodecyl sulfa

16 Southwestern blot analysis indicated that mPy protein is

17 Southwestern blot analysis indicated that the VIPR repre

18 Southwestern blot analysis indicates that the levels of

19 Southwestern blot analysis revealed that the antisense s

20 UV cross-linking and Southwestern blot analysis showed that GAS-RE1 bound a 5

21 Western and Southwestern blot analysis showed that three nuclear pro

22 ts yielded a single protein of 52 kDa, while Southwestern blot analysis with MMP-2 RE1 demonstrated t

23 ncing, electrophoretic mobility shift assay, Southwestern blot analysis, and supershift EMSA confirm

24 By Southwestern blot analysis, the MAR-binding activity of

25 T enhancer binding protein (MEBP), 45 kDa by Southwestern blot analysis, was present in the nuclei of

26 identified two potential binding proteins by southwestern blot analysis.

27 This paper describes the use of Southwestern blot and DNA gel shift analyses with RBF pr

28 Southwestern blot and UV cross-linking analyses identifi

29 Southwestern blotting and UV-cross-linking studies showe

30 the DNA-binding protein by UV cross-linking, Southwestern blot, and antibody ablation/supershift assa

31 Southwestern blot, electromobility shift, and chromatin

32 ion, using glycerol gradient centrifugation, Southwestern blotting, electrophoretic mobility shift as

33 cts as judged by both gel mobility-shift and Southwestern blot experiments, and overexpression of MSN

34 Southwestern blotting experiments probing nuclear extrac

35 Southwestern blotting methods identified three major pol

36 Southwestern blots of HeLa nuclear proteins with both th

37 body supershift, by immunoprecipitation with Southwestern blot or with UV cross-linking analysis in v

38 ased on the results of experiments employing SouthWestern blotting, protein purification, "shift-shif

39 ft assays, UV-cross-linking experiments, and Southwestern blots reveal that a 105-kDa protein specifi

40 Southwestern blotting revealed a approximately 90-kDa pr

41 cate F2 and F3 bind SF-1; BLAST searches and Southwestern blotting suggest that NF-W2 may bind F1.

42 Southwestern blotting using this probe coupled with part

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