high salt buffer Search Results


1x tris buffered saline  (Thermo Fisher)
94
Thermo Fisher 1x tris buffered saline
1x Tris Buffered Saline, supplied by Thermo Fisher, 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/high+salt+buffer/TRIS-buffered+saline+(TBS%2C+high+salt)+pH+7%2E4/pm26647830-64-17-20
Average 94 stars, based on 1 article reviews
1x tris buffered saline - by Bioz Stars, 2026-10
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high salt chip buffer  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology high salt chip buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Chip Buffer, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high+salt+buffer/ChIP+Lysis+Buffer+High+Salt/pmc03976374-53-11-56
Average 93 stars, based on 1 article reviews
high salt chip buffer - by Bioz Stars, 2026-10
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tris  (Chem Impex International)
95
Chem Impex International tris
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
Tris, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high+salt+buffer/Tris(hydroxymethyl)aminomethane/pm36643556-41-0-7
Average 95 stars, based on 1 article reviews
tris - by Bioz Stars, 2026-10
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high salt buffer (hsb  (Nexogen Inc)
90
Nexogen Inc high salt buffer (hsb
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Buffer (Hsb, supplied by Nexogen Inc, 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/high+salt+buffer/high+salt+buffer++hsb/pm29194985-89-22-25
Average 90 stars, based on 1 article reviews
high salt buffer (hsb - by Bioz Stars, 2026-10
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high-salt buffer  (Nanogen Inc)
90
Nanogen Inc high-salt buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Buffer, supplied by Nanogen Inc, 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/high+salt+buffer/high+salt+buffer/pmc02643657-189-50-52
Average 90 stars, based on 1 article reviews
high-salt buffer - by Bioz Stars, 2026-10
90/100 stars
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formamide high-salt buffer  (Schuell GmbH)
90
Schuell GmbH formamide high-salt buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
Formamide High Salt Buffer, supplied by Schuell GmbH, 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/high+salt+buffer/formamide+high+salt+buffer/10__1128_slash_mcb__16__2__724-141-17-19
Average 90 stars, based on 1 article reviews
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high salt relaxation buffer  (Promega)
90
Promega high salt relaxation buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Relaxation Buffer, supplied by Promega, 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/high+salt+buffer/high+salt+relaxation+buffer/10__1074_slash_jbc__m007167200-74-14-34
Average 90 stars, based on 1 article reviews
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high-salt buffer  (Solarbio Inc)
90
Solarbio Inc high-salt buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Buffer, supplied by Solarbio Inc, 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/high+salt+buffer/high+salt+buffer/10__2147_slash_cmar__s252340-58-35-37
Average 90 stars, based on 1 article reviews
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high salt neutralisation buffer  (Univar USA Inc)
90
Univar USA Inc high salt neutralisation buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Neutralisation Buffer, supplied by Univar USA Inc, 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/high+salt+buffer/high+salt+neutralisation+buffer/pmc00150390-163-0-13
Average 90 stars, based on 1 article reviews
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high-salt stripping buffer  (Promega)
90
Promega high-salt stripping buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Stripping Buffer, supplied by Promega, 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/high+salt+buffer/high+salt+stripping+buffer/pmc05419160-367-6-9
Average 90 stars, based on 1 article reviews
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high salt rab reassembly buffer pi53113  (G Biosciences)
90
G Biosciences high salt rab reassembly buffer pi53113
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Rab Reassembly Buffer Pi53113, supplied by G Biosciences, 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/high+salt+buffer/high+salt+rab+reassembly+buffer+pi53113/pmc09437221-59-14-20
Average 90 stars, based on 1 article reviews
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high salt immune complex wash buffer  (Upstate Biotechnology Inc)
86
Upstate Biotechnology Inc high salt immune complex wash buffer
(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), <t>ChIP</t> experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments <t>cross-linked</t> <t>chromatin</t> was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).
High Salt Immune Complex Wash Buffer, supplied by Upstate Biotechnology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high+salt+buffer/buffer+complex+high+immune+salt+wash/10__1158_slash_0008___5472__can___05___2481-47-20-26
Average 86 stars, based on 1 article reviews
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(A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), ChIP experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments cross-linked chromatin was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).

Journal: PLoS ONE

Article Title: Nucleosomes Are Stably Evicted from Enhancers but Not Promoters upon Induction of Certain Pro-Inflammatory Genes in Mouse Macrophages

doi: 10.1371/journal.pone.0093971

Figure Lengend Snippet: (A and B), Nucleosome occupancy at a putative enhancer 10 kb upstream of the TSS of IL1A was determined in BMDMs prior to (blue bars and lines) and upon 1.5 h (yellow) or 3 h (red) induction with 1 μg/ml LPS as described in the legend of . ConSite predicted consensus sites for PU.1, C/EBP, IRF, AP1 and NFκB are indicated. (C and D), Nucleosome occupancy at the promoter of IL1A was determined as described in panel (A) in a region surrounding the TSS of IL1A. The TSS (black bar) and a putative TATA-box (blue bar) is indicated in panel (C). (E), Kinetics of nucleosome removal at IL1A and IL12B. BMDMs were induced with LPS for 15′, 30′, 60′ and 90′, and nucleosome occupancy was analyzed as described in (A). Nucleosome removal at three locations in the distal enhancer of IL12B (red lines) and in the enhancer of IL1A (blue lines) is shown. The data is displayed as the fold change in nucleosome occupancy over the levels found before induction at each location. The absence of changes in nucleosome occupancy at the TSS of IL12B (black line) and of IL1A (gray line) is shown for comparison. (F), ChIP experiments with antibodies against H3 (dark blue bars), H2A.Z (light blue), H3K4me1 (green), H3K4me3 (yellow) and H3K27ac (red) were performed as described in the . For these experiments cross-linked chromatin was lightly digested with MNase before incubation with the respective antibodies to increase resolution of the ChIP signal and the data was normalized to a region in the ORF of RPL4. Changes upon LPS induction in histone binding and histone modifications at the enhancers and promoters of IL12B and IL1A as well as at a control region in the GAPDH pseudo gene are shown as fold over levels found before induction. For H3K27ac the changes 1.5 h after LPS induction, and for all other histone variants and modifications the changes after 3 h of induction are shown. The error bars show the SEM of at least 3 independent experiments. Statistical significance of the changes in H3K4me3 and H3K27ac upon LPS induction compared to levels found prior to induction determined by Student's T-tests is indicated (*P<0.05; **P<0.01).

Article Snippet: For all other ChIP experiments isolated chromatin was directly diluted with High Salt ChIP buffer and incubated with either 1 μg of anti-PolI antibody (sc-56767), 6 μg anti-TBP (sc-204), 4 μg anti-PU.1 (sc-352), 4 μg anti-C/EBPβ (sc-150), 6 μg anti-NFκB (sc-372), 5 μg anti-c-Jun (sc-45), 6 μg anti-p300 (sc-585) or 10 μg anti-IRF3 (sc-9082) all from Santa Cruz Biotechnologies.

Techniques: Comparison, Incubation, Binding Assay, Control

(A and B), ChIP experiments were performed as described in the legend of with antibodies that detect (A) PolII or (B) TBP in BMDMs before (dark blue bars), and upon 1.5 h (yellow) or 3 h (red) LPS induction. Cross-linked chromatin was either untreated (solid bars), or lightly digested with MNase (hatched bars) as described in the . The data was normalized to a region in the KIT promoter and genomic locations are indicated. The experiment was performed twice and error bars indicating the SEM are shown.

Journal: PLoS ONE

Article Title: Nucleosomes Are Stably Evicted from Enhancers but Not Promoters upon Induction of Certain Pro-Inflammatory Genes in Mouse Macrophages

doi: 10.1371/journal.pone.0093971

Figure Lengend Snippet: (A and B), ChIP experiments were performed as described in the legend of with antibodies that detect (A) PolII or (B) TBP in BMDMs before (dark blue bars), and upon 1.5 h (yellow) or 3 h (red) LPS induction. Cross-linked chromatin was either untreated (solid bars), or lightly digested with MNase (hatched bars) as described in the . The data was normalized to a region in the KIT promoter and genomic locations are indicated. The experiment was performed twice and error bars indicating the SEM are shown.

Article Snippet: For all other ChIP experiments isolated chromatin was directly diluted with High Salt ChIP buffer and incubated with either 1 μg of anti-PolI antibody (sc-56767), 6 μg anti-TBP (sc-204), 4 μg anti-PU.1 (sc-352), 4 μg anti-C/EBPβ (sc-150), 6 μg anti-NFκB (sc-372), 5 μg anti-c-Jun (sc-45), 6 μg anti-p300 (sc-585) or 10 μg anti-IRF3 (sc-9082) all from Santa Cruz Biotechnologies.

Techniques: