ライフサイエンスコーパス: far-Western blot

1 wild-type but not kinase-inactive JAK2 in a far Western blot.

2 ith Ace from OG1RF mutanolysin extracts on a far-Western blot.

3 PAK2 with CIN85 SH3 domains was confirmed by Far Western blotting.

4 interaction based on Far Western and reverse Far Western blotting.

5 ne, immunoprecipitation, immunoblotting, and far-Western blotting.

6 action of VirB9 and VirB6-2 was confirmed by far-Western blotting.

7 and LAT upon CRP stimulation of platelets by far-Western blotting.

8 nd that comigrated with that detected by pTP far-Western blotting.

9 system was in contrast to a strong signal by far-Western blotting.

10 t binding to the NM could be demonstrated by far-Western blotting.

11 acts directly with DNA polymerase beta using far Western blotting, affinity precipitation and yeast t

12 tein experiments, coimmunoprecipitations and Far Western blot analyses to demonstrate direct binding

13 the domain of VP2 required for binding VP1, far-Western blot analyses using a series of truncated VP

14 Far Western blot analysis also indicated that the SH3 do

15 Far Western blot analysis confirmed the specific binding

16 Far Western blot analysis confirms that SAPK/JNK binds d

17 Coimmunoprecipitation assays and far Western blot analysis demonstrate that this mutation

18 xperiments, subsequent studies using reverse Far Western blot analysis demonstrated that only the car

19 quiescent cells is probably not direct since Far Western blot analysis did not reveal the binding of

20 Moreover, Far Western blot analysis identified at least three AKAP

21 Far Western blot analysis implicates A190 of Pol I as we

22 Far Western blot analysis suggested that the tandem SH2

23 Far Western blot analysis was used to demonstrate the bi

24 Far Western blot analysis with either Nck, the SH2 domai

25 eningitidis strains was detected by FACS and Far Western blot analysis, and occurred in the absence o

26 This binding was confirmed by Far Western blot analysis, sedimentation on a glycerol g

27 Binding assays and far Western blotting analysis demonstrated association o

28 Binding assays and far Western blotting analysis, using glutathione S-trans

29 A protein (far Western) blot analysis revealed that dTAFIII105, pre

30 Here we used far-Western blot analysis and microscale thermophoresis

31 Far-Western blot analysis established that HMW1B interac

32 to bind only to the beta-subunit of eIF2 by far-Western blot analysis.

33 Using far-Western blotting analysis of chemically cleaved and

34 Furthermore, far-Western blotting analysis shows that SopE directly i

35 ombinant Fg chains and truncation mutants in Far Western blots and solid-phase binding assays.

36 Far Western blotting and two-hybrid analyses detect a di

37 Structure-function analyses using far-Western blot and transient cotransfection assays rev

38 n HPV type 11 (HPV-11) E1-binding protein by far-Western blotting and by microsequence analyses of a

39 The far-Western blotting and co-immunoprecipitation assays d

40 In far-Western blotting and guanine nucleotide saturation s

41 Initially, using a combination of far-western blotting and phosphoCTD affinity chromatogra

42 By Far-Western blotting and yeast two-hybrid assay, we demo

43 By far-Western blotting, and verified by coimmunoprecipitat

44 ): 1) phospho-specific mass spectrometry; 2) far-Western blotting; and 3) live cell single-molecule i

45 on of PCSK9 activity, and we demonstrated by far-Western blot assay that the M1 and M2 domains are ne

46 Using interaction "Far Western" blotting assays, we systematically tested f

47 o I in enzyme-linked immunosorbent assay and far-Western blot assays.

48 A was detected with the yeast two-hybrid and far-Western blot assays.

49 C10258 (MFn8, Lsa66), and LIC10537 (MFn9) by far-Western blot assays.

50 Far-Western blotting detected interaction of SATB1 and C

51 size from 120 to 200 kDa were identified on Far Western blots for their ability to bind pTP.

52 in-binding assay (VOPBA) in combination with far-Western blotting, gradient-purified EAV particles we

53 Comparative far Western blots have shown that hTAF(II)135 interacts

54 Far-Western blotting identified proteins of 150 and 240

55 Real-time polymerase chain reaction, (far) Western blot, immunoprecipitation, and immunocytoch

56 phosphorylation by quantitative Western and far-Western blotting, mass spectrometry, and computation

57 the pea aphid, Acyrthosiphon pisum, using a far-Western blot method.

58 type 3 (CR3, CD11b/CD18) was used to probe a Far Western blot of a detergent extract of Hc cell wall

59 recognized by DC, VLA-5 was used to probe a Far Western blot of a yeast freeze/thaw extract (F/TE) t

60 interact tightly and specifically, both on a far Western blot of yeast vacuolar proteins and in the y

61 In "far Western" blots of mouse embryonic protein extracts,

62 sociates to amplify its functional capacity, far-Western blotting of cholangiocyte epithelial cell pr

63 Far-Western blotting of EBP50 isolated by two-dimensiona

64 ation experiments with knockdown of GAB2 and Far-Western blots proved the direct interaction of SHP2

65 Far Western blotting revealed the presence of an approxi

66 Using the peptides as probes in far Western blots showed direct binding of the phosphory

67 ELISA and Far Western blotting showed that recombinant vimentin bo

68 Far Western blotting showed that this interaction was li

69 xible competitive binding assay based on the far-Western blot technique, in which a battery of Src ho

70 Moreover, far Western blotting using platelet membrane proteins re

71 Using copurification analysis and far-Western blotting, we found that Asp2 and Asp3 could

72 Interacting protein partners indicated by far-Western blotting were confirmed by immunoprecipitati

73 Far Western blotting with a CRKL-SH3 glutathione S-trans