1 bout 55 have DNA-binding sites identified by
DNA footprinting.
2 DNA footprinting also showed specific protection of the
3 We show by both mutational and
DNA footprinting analyses that the binding of nogalamyci
4 DNA footprinting analysis further demonstrated the speci
5 DNA footprinting analysis identified unique protein bind
6 DNA footprinting analysis of the cII transgene in AFB(1)
7 DNA footprinting analysis revealed a 37-bp region that i
8 Here we show by
DNA footprinting analysis that MPG, but not UDG, bound t
9 ng at the CR and M promoters was analyzed by
DNA footprinting and a range of biophysical techniques.
10 Exonuclease III mediated in vivo
DNA footprinting and dimethyl sulfate in vivo footprinti
11 We have used
DNA footprinting and fluorescence melting experiments to
12 By
DNA footprinting and gel retardation analysis, we demons
13 ron endonuclease with its DNA target site by
DNA footprinting and modification-interference approache
14 DNA footprinting and nuclease protection studies of PcrA
15 proximately 20 bp from the dyad was shown by
DNA footprinting and photoaffinity labeling using recomb
16 DNA footprinting and purine-base interference assays dem
17 DNA footprinting and single-molecule fluorescence experi
18 interactions with nucleosomes were mapped by
DNA footprinting and site-directed DNA and protein cross
19 egion I-deleted sigma holoenzyme observed by
DNA footprinting,
and are likely of significance to the
20 Biochemical,
DNA footprinting,
and in vitro transcription assays indi
21 teraction evaluated by thermal denaturation,
DNA footprinting,
and in vitro transcription stop assays
22 ation interference, modification protection,
DNA footprinting,
and photocross-linking techniques.
23 Using
DNA footprinting as an assay, we show here that PriA als
24 Gel shift and
DNA footprinting assays demonstrate that the SspA protei
25 Furthermore, methylation interference
DNA footprinting assays showed increased nuclear protein
26 ies using electrophoretic mobility shift and
DNA footprinting assays showed that both Sp1 and Sp3 pro
27 nal fusion, gel mobility shift analyses, and
DNA footprinting assays were used to confirm the direct
28 electrophoresis, immunodot blot assays, and
DNA footprinting assays, we demonstrated a unique wavele
29 DNA footprinting confirmed that interaction of Dda with
30 DNA footprinting confirmed that MprA protected large sec
31 In vivo genomic
DNA footprinting confirms the presence of nuclear protei
32 Results of in vivo genomic
DNA footprinting experiments indicate that a protein(s)
33 DNA footprinting experiments revealed similarities betwe
34 Molecular docking simulations and
DNA footprinting experiments suggest a model where a PC4
35 DNA footprinting experiments were also conducted to furt
36 Previous
DNA footprinting experiments with C.AhdI have located th
37 region of A-tracts, a feature inferred from
DNA footprinting experiments.
38 osines protected by in vivo dimethyl sulfate
DNA footprinting (
GAAGAGTG) in a luciferase construct (-
39 Hydroxyl radical
DNA footprinting indicated that the site-specifically bo
40 ctrophoretic mobility shift assay (EMSA) and
DNA footprinting,
members of the Sp family (Sp1, Sp3, an
41 DNA footprinting of EcoSSB on wild-type and mutant promo
42 Using in vivo genomic
DNA footprinting of normal human epithelial cells (HaCaT
43 High-resolution
DNA footprinting of the DNA product of transposition att
44 DNA footprinting of the JBP.J-DNA complex with 1,10-phen
45 Using
DNA footprinting of the regions upstream of the liaXYZ a
46 Through systematic
DNA footprinting of the TNF (encoding tumour necrosis fa
47 DNA footprinting of the TxRE with 1, 10-phenanthroline-c
48 DNA footprinting of this fragment revealed a highly cons
49 of the phosphodiester backbone resulted in a
DNA-footprinting pattern similar to that observed with t
50 To test this, we analyzed pelA
DNA footprinting patterns with various combinations of F
51 he results from Western blotting, EMSAs, and
DNA footprinting reactions lead to the conclusion that A
52 of the protein-DNA interface by quantitative
DNA footprinting revealed new minor groove contacts and
53 DNA footprinting revealed that a major conformational di
54 nterrogation of the protein/DNA interface by
DNA footprinting showed similar accessibility to dimethy
55 Protein-
DNA footprinting showed that both genes were occupied by
56 In vivo
DNA footprinting shows a specific loss of occupancy at t
57 DNA footprinting studies confirmed the specific binding
58 DNA footprinting studies of PhoP-regulated promoters sho
59 DNA footprinting studies suggest that the RAG proteins i
60 ts of electrophoretic mobility shift assays,
DNA footprinting studies, and promoter-lac fusion experi
61 We also show using
DNA footprinting studies, that T7 ligase binds asymmetri
62 We have prepared novel
DNA footprinting substrates that contain all 64 symmetri
63 Using in-gel cleavage assays and
DNA footprinting techniques, I analyzed the catalytic ac
64 SWI/SNF was found by
DNA footprinting to contact tightly around one gyre of D
65 se electrophoretic mobility shift assays and
DNA footprinting to show that the DrHU N-terminal domain
66 DNA footprinting using exonucleaseIII and DNaseI, and me
67 died using equilibrium binding measurements,
DNA footprinting,
van't Hoff analysis and calorimetry.
68 As another approach, in vivo
DNA footprinting was used and identified protein protect
69 The advent of
DNA footprinting with DNase I more than 35 years ago ena