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superdex 200 increase 10 300 gl  (Cytiva Europe)
99
Cytiva Europe superdex 200 increase 10 300 gl
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
Superdex 200 Increase 10 300 Gl, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/Superdex+200+Increase+SEC+column/pmc13596708-655-0-6
Average 99 stars, based on 1 article reviews
superdex 200 increase 10 300 gl - by Bioz Stars, 2026-11
99/100 stars
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superdex 200 increase 10 300 gl column  (Cytiva Europe)
99
Cytiva Europe superdex 200 increase 10 300 gl column
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
Superdex 200 Increase 10 300 Gl Column, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/Superdex+200+Increase+SEC+column/pmc12988193-22-0-7
Average 99 stars, based on 1 article reviews
superdex 200 increase 10 300 gl column - by Bioz Stars, 2026-11
99/100 stars
  Buy from Supplier
superdex 200 increase  (Cytiva Europe)
94
Cytiva Europe superdex 200 increase
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
Superdex 200 Increase, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/Superdex+30+Increase+10%2F300+GL/pm41361696-260-15-20
Average 94 stars, based on 1 article reviews
superdex 200 increase - by Bioz Stars, 2026-11
94/100 stars
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superdex 200 increase 10 300 gl gel filtration column  (Cytiva Europe)
99
Cytiva Europe superdex 200 increase 10 300 gl gel filtration column
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
Superdex 200 Increase 10 300 Gl Gel Filtration Column, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/Superdex+200+Increase+SEC+column/pmc12719664-29-8-17
Average 99 stars, based on 1 article reviews
superdex 200 increase 10 300 gl gel filtration column - by Bioz Stars, 2026-11
99/100 stars
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superdex 200 increase 10 300 gl size exclusion chromatography column  (Cytiva Europe)
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Cytiva Europe superdex 200 increase 10 300 gl size exclusion chromatography column
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
Superdex 200 Increase 10 300 Gl Size Exclusion Chromatography Column, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/Superdex+200+Increase+SEC+column/pmc12648108-213-0-10
Average 99 stars, based on 1 article reviews
superdex 200 increase 10 300 gl size exclusion chromatography column - by Bioz Stars, 2026-11
99/100 stars
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10 300 gl column  (Cytiva Europe)
99
Cytiva Europe 10 300 gl column
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
10 300 Gl Column, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/Superdex+200+Increase+SEC+column/pm41022699-219-17-21
Average 99 stars, based on 1 article reviews
10 300 gl column - by Bioz Stars, 2026-11
99/100 stars
  Buy from Supplier
superdex 200 10 300 gl increase column  (Cytiva Europe)
99
Cytiva Europe superdex 200 10 300 gl increase column
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
Superdex 200 10 300 Gl Increase Column, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/Superdex+200+Increase+SEC+column/pmc13632693-1010-0-6
Average 99 stars, based on 1 article reviews
superdex 200 10 300 gl increase column - by Bioz Stars, 2026-11
99/100 stars
  Buy from Supplier
superdex 200 increase 10/300 gl column  (Cytiva Europe)
90
Cytiva Europe superdex 200 increase 10/300 gl column
(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in <t>Superdex</t> <t>200</t> increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography
Superdex 200 Increase 10/300 Gl Column, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superdex+200+10+%E2%81%84+300+gl/superdex+200+increase+10+300+gl+column/pmc09427005__abn8652_sm-47-55-56
Average 90 stars, based on 1 article reviews
superdex 200 increase 10/300 gl column - by Bioz Stars, 2026-11
90/100 stars
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(a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in Superdex 200 increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography

Journal: Molecular cell

Article Title: BRD4 binds the nucleosome via both histone and DNA interactions

doi: 10.1016/j.molcel.2026.07.012

Figure Lengend Snippet: (a) BRD4 BD1 interactions with the nucleosome with key regions highlighted, (b) TR-FRET dissociation constants for BRD4-S bromodomain mutants binding to H4 K12acK16ac nucleosomes, (c) model for how BRD4 basic region 1 could interact with nucleosome DNA minor groove with C α positions of the 5 basic residues shown in blue spheres, (d) effect of BRD4-S BD1 mutations on BRD4-S/nucleosome complex mobility in gel mobility shift assay, (e) NMR structure of HMG-I(Y) AT-hook Arg-Gly-Arg region binding to DNA (PDB ID 2EZD), protein residues outside of the Arg-Gly-Arg region not shown, (f) TR-FRET dissociation constants for BRD4-S basic patch 1 mutants binding to H4 K12acK16ac nucleosomes, (g) the BRD4-S WT/H4 K12acK16 ac nucleosome complex elutes slightly later than the BRD4-S WT/WT nucleosome complex (peak elution of 9.8 vs 9.6 ml) in Superdex 200 increase size-exclusion chromatography, (h) the BRD4-S m12/H4 K12acK16ac nucleosome complex (blue) elutes earlier than the BRD4-S WT/H4 K12acK16ac nucleosome complex in Superdex 200 increase size-exclusion chromatography, (i) the BRD4-S m12 protein elutes at similar time as the BRD4 WT protein in Superdex 200 increase size-exclusion chromatography

Article Snippet: Superdex 200 Increase 10/300 GL , GE Healthcare , Cat# 28-9909-44.

Techniques: Binding Assay, Mobility Shift, Size-exclusion Chromatography