Review



chip dna clean concentrator kit  (Zymo Research)


Bioz Verified Symbol Zymo Research is a verified supplier
Bioz Manufacturer Symbol Zymo Research manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 99

    Structured Review

    Zymo Research chip dna clean concentrator kit
    Chip Dna Clean Concentrator Kit, supplied by Zymo Research, used in various techniques. Bioz Stars score: 99/100, based on 1500 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/pmc13109728-100-15-21
    Average 99 stars, based on 1500 article reviews
    chip dna clean concentrator kit - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Chromatin Immunoprecipitation:

    Article Title: Protocol for chromatin immunoprecipitation using isolated antheridia of Marchantia polymorpha
    Article Snippet: HiYield Gel/PCR DNA Fragments Extraction Kit , RBC Bioscience , Cat#YDF300. .. ChIP DNA Clean & Concentrator , ZYMO RESEARCH , Cat#D5201. .. KOD SYBR qPCR Mix , TOYOBO , Cat#QKD-201.

    Article Title: Regulation of oncogenic C-terminal truncated p53β protein isoform expression by SRSF3–UPF1 splicing and surveillance axis
    Article Snippet: .. Samples were then treated with 400 μg/mL RNase A (Thermo Fisher, #EN0531) at 37 °C for 45 min, followed by protein digestion with 200 μg/mL protease K—50 mM Tris–HCl at pH 7.5 and 10 mM EDTA—at 65 °C for 1 h. DNA was purified using ChIP DNA Clean & Concentrator (Zymo Research, #D5205). .. Subsequently, reverse transcription was performed with SuperscriptTM IV Reverse Transcriptase (Invitrogen, #18,090,010), and qPCR was performed on a StepOneTM Real-time PCR system (Applied Biosystems).

    Article Title: Co-option of a mouse-specific retrotransposon rewires Ash2l isoform usage to prime developmental promoters
    Article Snippet: .. The input sample was treated with proteinase K (NEB) overnight at 65°C and purified using Zymo ChIP DNA Clean & Concentrator, and used to check for sonication efficiency. ..

    Article Title: Protocol for chromatin immunoprecipitation using isolated antheridia of Marchantia polymorpha.
    Article Snippet: .. Note: This protocol used the ChIP DNA Clean & Concentrator from ZYMO RESEARCH, following the manufacturer’s instruction (https://files.zymoresearch.com/protocols/ _d5201_d5205_chip_dna_clean_concentrator_kit.pdf). ..

    Article Title: Protocol for chromatin immunoprecipitation using isolated antheridia of Marchantia polymorpha
    Article Snippet: .. Note: This protocol used the ChIP DNA Clean & Concentrator from ZYMO RESEARCH, following the manufacturer’s instruction ( https://files.zymoresearch.com/protocols/_d5201_d5205_chip_dna_clean_concentrator_kit.pdf ). ..

    Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice
    Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl 2 for 1 h. Precipitated chromatin DNA was purified using ChIP DNA Clean & Concentrator (ZYMO Research). .. Purified DNA was subjected to the quantification of E4 , S4 region with PowerUp SYBR Green Master Mix (Thermo Fisher Scientific), QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific) and the following specific primers (Eurofins Genomics); E4p -F: 5′-TCTCCAAAGGGTAACAGGTGTCAG-3′, E4p -R: 5′-TGTGACTTACAAAGGTGCCTCCA-3′, S4 -F: 5′-CCTTGTGTGGTCCCTCTCTTTG-3′, S4 -R: 5′-GCAACAACCACCCTTCACAGG-3′, Alb -F: 5′-ACCTGCGTTACAGCATCCAC-3′, and Alb -R: 5′-TGCTGACAGAGCAGGAGACA-3′.

    Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice.
    Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl2 for 1 h. Precipitated chromatin DNA was purified using ChIP DNA Clean & Concentrator (ZYMO Research). .. Purified DNA was subjected to the quantification of E4, S4 region with PowerUp SYBR Green Master Mix (Thermo Fisher Scientific), QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific) and the following specific primers (Eurofins Genomics); E4p-F: 5′-TCTCCAAAGGGTAACAGGTGTCAG-3′, E4p-R: 5′-TGTGACTTACAAAGGTGCCTCCA-3′, S4-F: 5′-CCTTGTG TGGTCCCTCTCTTTG-3′, S4-R: 5′-GCAACAACCACCCTTCACAGG-3′, Alb-F: 5′-ACCTGCGTTACAGCATCCAC-3′, and Alb-R: 5′-TGCTGACA GAGCAGGAGACA-3′.

    Purification:

    Article Title: Regulation of oncogenic C-terminal truncated p53β protein isoform expression by SRSF3–UPF1 splicing and surveillance axis
    Article Snippet: .. Samples were then treated with 400 μg/mL RNase A (Thermo Fisher, #EN0531) at 37 °C for 45 min, followed by protein digestion with 200 μg/mL protease K—50 mM Tris–HCl at pH 7.5 and 10 mM EDTA—at 65 °C for 1 h. DNA was purified using ChIP DNA Clean & Concentrator (Zymo Research, #D5205). .. Subsequently, reverse transcription was performed with SuperscriptTM IV Reverse Transcriptase (Invitrogen, #18,090,010), and qPCR was performed on a StepOneTM Real-time PCR system (Applied Biosystems).

    Article Title: Co-option of a mouse-specific retrotransposon rewires Ash2l isoform usage to prime developmental promoters
    Article Snippet: .. The input sample was treated with proteinase K (NEB) overnight at 65°C and purified using Zymo ChIP DNA Clean & Concentrator, and used to check for sonication efficiency. ..

    Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice
    Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl 2 for 1 h. Precipitated chromatin DNA was purified using ChIP DNA Clean & Concentrator (ZYMO Research). .. Purified DNA was subjected to the quantification of E4 , S4 region with PowerUp SYBR Green Master Mix (Thermo Fisher Scientific), QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific) and the following specific primers (Eurofins Genomics); E4p -F: 5′-TCTCCAAAGGGTAACAGGTGTCAG-3′, E4p -R: 5′-TGTGACTTACAAAGGTGCCTCCA-3′, S4 -F: 5′-CCTTGTGTGGTCCCTCTCTTTG-3′, S4 -R: 5′-GCAACAACCACCCTTCACAGG-3′, Alb -F: 5′-ACCTGCGTTACAGCATCCAC-3′, and Alb -R: 5′-TGCTGACAGAGCAGGAGACA-3′.

    Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice.
    Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl2 for 1 h. Precipitated chromatin DNA was purified using ChIP DNA Clean & Concentrator (ZYMO Research). .. Purified DNA was subjected to the quantification of E4, S4 region with PowerUp SYBR Green Master Mix (Thermo Fisher Scientific), QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific) and the following specific primers (Eurofins Genomics); E4p-F: 5′-TCTCCAAAGGGTAACAGGTGTCAG-3′, E4p-R: 5′-TGTGACTTACAAAGGTGCCTCCA-3′, S4-F: 5′-CCTTGTG TGGTCCCTCTCTTTG-3′, S4-R: 5′-GCAACAACCACCCTTCACAGG-3′, Alb-F: 5′-ACCTGCGTTACAGCATCCAC-3′, and Alb-R: 5′-TGCTGACA GAGCAGGAGACA-3′.

    Sonication:

    Article Title: Co-option of a mouse-specific retrotransposon rewires Ash2l isoform usage to prime developmental promoters
    Article Snippet: .. The input sample was treated with proteinase K (NEB) overnight at 65°C and purified using Zymo ChIP DNA Clean & Concentrator, and used to check for sonication efficiency. ..

    other:

    Article Title: Regulation of oncogenic C-terminal truncated p53β protein isoform expression by SRSF3-UPF1 splicing and surveillance axis.
    Article Snippet: Supernatants were diluted 5-fold with immunoprecipitation (IP) dilution buffer—20 mM Tris-HCl at pH 8.0, 150 mM NaCl, 1 mM EDTA, and 1% Triton X-100—and incubated overnight at 4°C with anti-FLAG-M2 affinity gel (Sigma, #A2220).

    Incubation:

    Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice
    Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl 2 for 1 h. Precipitated chromatin DNA was purified using ChIP DNA Clean & Concentrator (ZYMO Research). .. Purified DNA was subjected to the quantification of E4 , S4 region with PowerUp SYBR Green Master Mix (Thermo Fisher Scientific), QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific) and the following specific primers (Eurofins Genomics); E4p -F: 5′-TCTCCAAAGGGTAACAGGTGTCAG-3′, E4p -R: 5′-TGTGACTTACAAAGGTGCCTCCA-3′, S4 -F: 5′-CCTTGTGTGGTCCCTCTCTTTG-3′, S4 -R: 5′-GCAACAACCACCCTTCACAGG-3′, Alb -F: 5′-ACCTGCGTTACAGCATCCAC-3′, and Alb -R: 5′-TGCTGACAGAGCAGGAGACA-3′.

    Article Title: Phosphorylation of Runx protein controls helper CD4 + T cell versus cytotoxic CD8 + T cell lineage choice.
    Article Snippet: .. Samples were treated with RNaseA (Thermo Fisher Scientific) at 37 °C for 2 h followed by incubation with Proteinase K (Thermo Fisher Scientific) at 55 °C in the presence of 6 mM CaCl2 for 1 h. Precipitated chromatin DNA was purified using ChIP DNA Clean & Concentrator (ZYMO Research). .. Purified DNA was subjected to the quantification of E4, S4 region with PowerUp SYBR Green Master Mix (Thermo Fisher Scientific), QuantStudio 3 Real-Time PCR System (Thermo Fisher Scientific) and the following specific primers (Eurofins Genomics); E4p-F: 5′-TCTCCAAAGGGTAACAGGTGTCAG-3′, E4p-R: 5′-TGTGACTTACAAAGGTGCCTCCA-3′, S4-F: 5′-CCTTGTG TGGTCCCTCTCTTTG-3′, S4-R: 5′-GCAACAACCACCCTTCACAGG-3′, Alb-F: 5′-ACCTGCGTTACAGCATCCAC-3′, and Alb-R: 5′-TGCTGACA GAGCAGGAGACA-3′.



    Similar Products

    99
    Zymo Research chip dna clean concentrator kit
    Chip Dna Clean Concentrator Kit, supplied by Zymo Research, 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/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/pmc13109728-100-15-21
    Average 99 stars, based on 1 article reviews
    chip dna clean concentrator kit - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    Zymo Research chip dna clean and concentrator kit 319
    Chip Dna Clean And Concentrator Kit 319, supplied by Zymo Research, 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/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/pm42051138-172-7-6
    Average 99 stars, based on 1 article reviews
    chip dna clean and concentrator kit 319 - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    Zymo Research chip dna concentrator columns
    Chip Dna Concentrator Columns, supplied by Zymo Research, 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/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/us12612662-369-6-10
    Average 99 stars, based on 1 article reviews
    chip dna concentrator columns - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    Zymo Research chip dna clean and concentrator kit
    Chip Dna Clean And Concentrator Kit, supplied by Zymo Research, 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/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/bio_rxiv__64898__2026__04__16__718857-212-6-12
    Average 99 stars, based on 1 article reviews
    chip dna clean and concentrator kit - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    Zymo Research chip dna clean and concentration kit
    Chip Dna Clean And Concentration Kit, supplied by Zymo Research, 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/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/pmc13049674-547-38-44
    Average 99 stars, based on 1 article reviews
    chip dna clean and concentration kit - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    Zymo Research chip dna
    A, Phylogeny of the species used in this study. B, ChromHMM emissions plot and genomic coverage for human round spermatid (RS) chromatin state maps. C, Example genome browser tracks (hg38) of chromatin states defined by the ChromHMM model. D, Quantitative H3K4me3 and H3K27me3 <t>ChIP-seq</t> signal information for individual regions defined by ChromHMM (see Methods). Color represents functional annotation (FA) of the ChromHMM state. E, Total genomic coverage in megabases (Mb) of bivalent regions across species. F, Fraction of promoters (+/- 1kb around TSS) which overlap with a bivalent domain. Total numbers of promoters: human n=86,363, rhesus n=35,419, mouse n=78,296, rat n=32,862, bull n=36,068, opossum n=30,367. G, Expression level (FPKM) of genes with promoters marked by a given chromatin state in human RS. Box shows median and interquartile range; whiskers show range of the distribution. *p < 1e-10, 1-sample t-test performed (alternative=”less”) against the mean expression of all genes (dashed line). H, GC content of individual regions within each FA type. *p < 1e-30, 1-sample t-test performed (alternative=”greater”) against the mean whole-genome GC content (hg38, dashed line). I, Mean phastCons score within individual regions by FA type. *p < 1e-30, 1-sample t-test performed (alternative=”less”) against the mean of a set of re-shuffled regions in the human genome (hg38, dashed line). J, Genomic enrichment (odds ratio) of CpG islands, promoters, and repeat elements (LINE/SINE/LTR) in bivalent elements across species (see Methods). K, Position weight matrix of the ten most frequent enriched <t>DNA</t> motifs found in human bivalent regions near promoters (n=10,000). For each enriched de-novo motif, frequency in the test set (left), motif E-value (-log10) (middle), and number of predicted TFs (right) are shown.
    Chip Dna, supplied by Zymo Research, 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/chip+dna+clean+concentrator/ChIP+DNA+Clean+%26+Concentrator/bio_rxiv__64898__2026__04__14__718508-232-0-6
    Average 99 stars, based on 1 article reviews
    chip dna - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    Image Search Results


    A, Phylogeny of the species used in this study. B, ChromHMM emissions plot and genomic coverage for human round spermatid (RS) chromatin state maps. C, Example genome browser tracks (hg38) of chromatin states defined by the ChromHMM model. D, Quantitative H3K4me3 and H3K27me3 ChIP-seq signal information for individual regions defined by ChromHMM (see Methods). Color represents functional annotation (FA) of the ChromHMM state. E, Total genomic coverage in megabases (Mb) of bivalent regions across species. F, Fraction of promoters (+/- 1kb around TSS) which overlap with a bivalent domain. Total numbers of promoters: human n=86,363, rhesus n=35,419, mouse n=78,296, rat n=32,862, bull n=36,068, opossum n=30,367. G, Expression level (FPKM) of genes with promoters marked by a given chromatin state in human RS. Box shows median and interquartile range; whiskers show range of the distribution. *p < 1e-10, 1-sample t-test performed (alternative=”less”) against the mean expression of all genes (dashed line). H, GC content of individual regions within each FA type. *p < 1e-30, 1-sample t-test performed (alternative=”greater”) against the mean whole-genome GC content (hg38, dashed line). I, Mean phastCons score within individual regions by FA type. *p < 1e-30, 1-sample t-test performed (alternative=”less”) against the mean of a set of re-shuffled regions in the human genome (hg38, dashed line). J, Genomic enrichment (odds ratio) of CpG islands, promoters, and repeat elements (LINE/SINE/LTR) in bivalent elements across species (see Methods). K, Position weight matrix of the ten most frequent enriched DNA motifs found in human bivalent regions near promoters (n=10,000). For each enriched de-novo motif, frequency in the test set (left), motif E-value (-log10) (middle), and number of predicted TFs (right) are shown.

    Journal: bioRxiv

    Article Title: Ancestral chromatin state constrains the functional landscape of bivalent domains in mammalian spermatogenesis

    doi: 10.64898/2026.04.14.718508

    Figure Lengend Snippet: A, Phylogeny of the species used in this study. B, ChromHMM emissions plot and genomic coverage for human round spermatid (RS) chromatin state maps. C, Example genome browser tracks (hg38) of chromatin states defined by the ChromHMM model. D, Quantitative H3K4me3 and H3K27me3 ChIP-seq signal information for individual regions defined by ChromHMM (see Methods). Color represents functional annotation (FA) of the ChromHMM state. E, Total genomic coverage in megabases (Mb) of bivalent regions across species. F, Fraction of promoters (+/- 1kb around TSS) which overlap with a bivalent domain. Total numbers of promoters: human n=86,363, rhesus n=35,419, mouse n=78,296, rat n=32,862, bull n=36,068, opossum n=30,367. G, Expression level (FPKM) of genes with promoters marked by a given chromatin state in human RS. Box shows median and interquartile range; whiskers show range of the distribution. *p < 1e-10, 1-sample t-test performed (alternative=”less”) against the mean expression of all genes (dashed line). H, GC content of individual regions within each FA type. *p < 1e-30, 1-sample t-test performed (alternative=”greater”) against the mean whole-genome GC content (hg38, dashed line). I, Mean phastCons score within individual regions by FA type. *p < 1e-30, 1-sample t-test performed (alternative=”less”) against the mean of a set of re-shuffled regions in the human genome (hg38, dashed line). J, Genomic enrichment (odds ratio) of CpG islands, promoters, and repeat elements (LINE/SINE/LTR) in bivalent elements across species (see Methods). K, Position weight matrix of the ten most frequent enriched DNA motifs found in human bivalent regions near promoters (n=10,000). For each enriched de-novo motif, frequency in the test set (left), motif E-value (-log10) (middle), and number of predicted TFs (right) are shown.

    Article Snippet: ChIP DNA was purified using the Zymo ChIP DNA Clean & Concentrator kit (Zymo D5201) following manufacturer’s instructions.

    Techniques: ChIP-sequencing, Functional Assay, Expressing

    A, Frequencies of orthologous chromatin state combinations between ancestral species (bull, opossum; left) and primate species (rhesus, human; right). The most frequent states are shown based on n=19,953 total regions classified. B, Example genome browser tracks of representative examples of evolutionarily dynamic bivalency classes: conserved bivalent (left), ancestrally Polycomb (middle), and ancestrally active (right). C, Numbers of bivalent regions in each set of evolutionary classes defined in the primate lineage. D, GC content of individual human regions within each class of evolutionarily dynamic bivalent regions. Box shows median and interquartile range; whiskers show range of the distribution. Dashed line indicates mean GC content for all bivalent regions. All comparisons significantly different (p < 1e-30, two-sample, two-sided Kolmogorov-Smirnov test) except where indicated as “ns”. E, Quantitative H3K4me3 and H3K27me3 ChIP-seq signal in human bivalent regions color-coded by evolutionary class. Number of elements in each class as shown in (C). F, Genomic enrichment (odds ratio) of promoters, CpG islands, DNase+ H3K4me3 cCRE elements, and repeat elements (LINE/SINE/LTR) in distinct evolutionary classes of human bivalent elements. G, Fraction of human bivalent regions within an evolutionary class that have the indicated chromatin state in hESCs. Total number of elements within each set as shown in (C). *p < 0.05, Fisher’s exact test (alternative=’greater’) for comparison of co-occurrence between states. H, Position weight matrix of the most frequent enriched DNA-motifs found in human bivalent regions according to evolutionary label, with total number of elements as shown in (C), using all evolutionary classified regions as negative background set. For each enriched motif, frequency in the test set (left) and motif E-value (-log10) (right) is shown (Methods). *p < 0.05.

    Journal: bioRxiv

    Article Title: Ancestral chromatin state constrains the functional landscape of bivalent domains in mammalian spermatogenesis

    doi: 10.64898/2026.04.14.718508

    Figure Lengend Snippet: A, Frequencies of orthologous chromatin state combinations between ancestral species (bull, opossum; left) and primate species (rhesus, human; right). The most frequent states are shown based on n=19,953 total regions classified. B, Example genome browser tracks of representative examples of evolutionarily dynamic bivalency classes: conserved bivalent (left), ancestrally Polycomb (middle), and ancestrally active (right). C, Numbers of bivalent regions in each set of evolutionary classes defined in the primate lineage. D, GC content of individual human regions within each class of evolutionarily dynamic bivalent regions. Box shows median and interquartile range; whiskers show range of the distribution. Dashed line indicates mean GC content for all bivalent regions. All comparisons significantly different (p < 1e-30, two-sample, two-sided Kolmogorov-Smirnov test) except where indicated as “ns”. E, Quantitative H3K4me3 and H3K27me3 ChIP-seq signal in human bivalent regions color-coded by evolutionary class. Number of elements in each class as shown in (C). F, Genomic enrichment (odds ratio) of promoters, CpG islands, DNase+ H3K4me3 cCRE elements, and repeat elements (LINE/SINE/LTR) in distinct evolutionary classes of human bivalent elements. G, Fraction of human bivalent regions within an evolutionary class that have the indicated chromatin state in hESCs. Total number of elements within each set as shown in (C). *p < 0.05, Fisher’s exact test (alternative=’greater’) for comparison of co-occurrence between states. H, Position weight matrix of the most frequent enriched DNA-motifs found in human bivalent regions according to evolutionary label, with total number of elements as shown in (C), using all evolutionary classified regions as negative background set. For each enriched motif, frequency in the test set (left) and motif E-value (-log10) (right) is shown (Methods). *p < 0.05.

    Article Snippet: ChIP DNA was purified using the Zymo ChIP DNA Clean & Concentrator kit (Zymo D5201) following manufacturer’s instructions.

    Techniques: ChIP-sequencing, Comparison