phase genomics open-source hi-c alignment qc tool Search Results


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HIGHLIGHTS
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OriGene med6 origene ta343540 ch12
(A) Genetic screen from mouse T, B and ES cells compared to yeast and the hMED minimal core. Essential subunits denoted with red boxes, non-essential with grey ones, minimal core subunits with checkmarks. (B) Bar graph shows the number of transcriptionally affected genes (>1.5 fold) in <t>CH12</t> B cells deficient for non-essential (non-tail) mMED subunits. (C) Schematic showing MED14-degron strategy. A SMASh tag consisting of a linker, the hepatitis C protease, and a degron subunit was fused to MED14-N terminus. In untreated cells, the protease frees MED14 from SMASh, which is degraded. The hepatitis C protease inhibitor Asunaprevir blocks SMASh cleavage leading to MED14 degradation. (D) Transcriptome analysis of APR-treated Med14SMASh vs. control cells. Red dots represent mRNA spike-ins used to normalize signals on a per cell basis. (E) Med26, PolII, PolII-S5, PolII-S2, H3K4me3, H3K4me1, and H3K27Ac ChIP-Seq profiles at the Xbp1 locus in APR-treated WT (left) or Med14SMASh (right) cells. The orientation of genes is denoted with red arrows.
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Carl Zeiss axiovisionx64 4.9.1.0
(A) Genetic screen from mouse T, B and ES cells compared to yeast and the hMED minimal core. Essential subunits denoted with red boxes, non-essential with grey ones, minimal core subunits with checkmarks. (B) Bar graph shows the number of transcriptionally affected genes (>1.5 fold) in <t>CH12</t> B cells deficient for non-essential (non-tail) mMED subunits. (C) Schematic showing MED14-degron strategy. A SMASh tag consisting of a linker, the hepatitis C protease, and a degron subunit was fused to MED14-N terminus. In untreated cells, the protease frees MED14 from SMASh, which is degraded. The hepatitis C protease inhibitor Asunaprevir blocks SMASh cleavage leading to MED14 degradation. (D) Transcriptome analysis of APR-treated Med14SMASh vs. control cells. Red dots represent mRNA spike-ins used to normalize signals on a per cell basis. (E) Med26, PolII, PolII-S5, PolII-S2, H3K4me3, H3K4me1, and H3K27Ac ChIP-Seq profiles at the Xbp1 locus in APR-treated WT (left) or Med14SMASh (right) cells. The orientation of genes is denoted with red arrows.
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Cell Signaling Technology Inc resource source identifier antibodies anti phospho histone h3 ser10 antibody cell signaling technology
(A) Genetic screen from mouse T, B and ES cells compared to yeast and the hMED minimal core. Essential subunits denoted with red boxes, non-essential with grey ones, minimal core subunits with checkmarks. (B) Bar graph shows the number of transcriptionally affected genes (>1.5 fold) in <t>CH12</t> B cells deficient for non-essential (non-tail) mMED subunits. (C) Schematic showing MED14-degron strategy. A SMASh tag consisting of a linker, the hepatitis C protease, and a degron subunit was fused to MED14-N terminus. In untreated cells, the protease frees MED14 from SMASh, which is degraded. The hepatitis C protease inhibitor Asunaprevir blocks SMASh cleavage leading to MED14 degradation. (D) Transcriptome analysis of APR-treated Med14SMASh vs. control cells. Red dots represent mRNA spike-ins used to normalize signals on a per cell basis. (E) Med26, PolII, PolII-S5, PolII-S2, H3K4me3, H3K4me1, and H3K27Ac ChIP-Seq profiles at the Xbp1 locus in APR-treated WT (left) or Med14SMASh (right) cells. The orientation of genes is denoted with red arrows.
Resource Source Identifier Antibodies Anti Phospho Histone H3 Ser10 Antibody Cell Signaling Technology, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc plko 1 egfp nt sg
(A) Genetic screen from mouse T, B and ES cells compared to yeast and the hMED minimal core. Essential subunits denoted with red boxes, non-essential with grey ones, minimal core subunits with checkmarks. (B) Bar graph shows the number of transcriptionally affected genes (>1.5 fold) in <t>CH12</t> B cells deficient for non-essential (non-tail) mMED subunits. (C) Schematic showing MED14-degron strategy. A SMASh tag consisting of a linker, the hepatitis C protease, and a degron subunit was fused to MED14-N terminus. In untreated cells, the protease frees MED14 from SMASh, which is degraded. The hepatitis C protease inhibitor Asunaprevir blocks SMASh cleavage leading to MED14 degradation. (D) Transcriptome analysis of APR-treated Med14SMASh vs. control cells. Red dots represent mRNA spike-ins used to normalize signals on a per cell basis. (E) Med26, PolII, PolII-S5, PolII-S2, H3K4me3, H3K4me1, and H3K27Ac ChIP-Seq profiles at the Xbp1 locus in APR-treated WT (left) or Med14SMASh (right) cells. The orientation of genes is denoted with red arrows.
Plko 1 Egfp Nt Sg, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


KEY RESOURCES TABLE

Journal: Molecular cell

Article Title: In vivo evidence for ATPase-dependent DNA translocation by the Bacillus subtilis SMC condensin complex

doi: 10.1016/j.molcel.2018.07.006

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Anti-SMC polyclonal rabbit antibody ( Lindow et al., 2002 ) N/A Anti-ParB polyclonal rabbit antibody ( Lin et al., 1997 ) N/A Anti-ScpA polyclonal rabbit antibody, affinity purified ( Wang et al., 2017 ) N/A Anti-ScpA polyclonal rabbit antibody, affinity purified ( Wang et al., 2017 ) N/A Anti-SigA polyclonal rabbit antibody ( Fujita, 2000 ) N/A Chemicals, Peptides, and Recombinant Proteins Benzonase EMD Cat # 7046 Ni-NTA agarose Qiagen Cat # 30230 HiTrap Q HP GE Healthcare Cat # 17115301 Bradford Assay Kit ThermoFisher Cat # 23236 ATP Dot Scientific Cat # DSA30030–5 NADH Acros Organic Cat # 271100010 Phosphoenolypyruvate Tokyo Chemical Industry Cat # P0256 Rabbit Pyruvate Kinase Roche Diagnostics Cat # 10109045001 Lactate Dehydrogenase Sigma, Darmstadt, Germany Cat # L2500–25KU Formaldehyde 37% Sigma Cat # F8775 Ready-Lyse Lysozyme Epicentre Cat # R1802M HindIII NEB Cat # R0104M Klenow NEB Cat # M0210L Biotin-14-dATP ThermoFisher Cat # 19524016 T4 DNA ligase NEB Cat # M0202M Proteinase K NEB Cat # P8107S T4 DNA Polymerase NEB Cat # M0203L Critical Commercial Assays ATPase/GTPase Activity Assay Kit Sigma Cat # MAK113 NEBNext Ultra II DNA Library Prep Kit NEB Cat # E7645S Deposited Data Raw and analyzed Hi-C data This paper GEO: {"type":"entrez-geo","attrs":{"text":"GSE95137","term_id":"95137"}} GSE95137 Original Data Mendeley Data http://dx.doi.org/10.17632/tygwp234gr.1 Experimental Models: Organisms/Strains Bacillus subtilis strains, see Table S1 Oligonucleotides See Table S3 Recombinant DNA See Table S2 Software and Algorithms MATLAB 8.5 (R2015) ( Wang et al., 2017 ) https://www.mathworks.com/ hiclib ( Imakaev et al., 2012 ) https://bitbucket.org/mirnylab/hiclib Open in a separate window KEY RESOURCES TABLE

Techniques: Affinity Purification, Recombinant, Bradford Assay, Activity Assay, Software

HIGHLIGHTS

Journal: Cell

Article Title: Extensive Heterogeneity and Intrinsic Variation in Spatial Genome Organization

doi: 10.1016/j.cell.2019.01.020

Figure Lengend Snippet: HIGHLIGHTS

Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Bacterial and Virus Strains Biological Samples Chemicals, Peptides, and Recombinant Proteins Critical Commercial Assays Deposited Data HFF-hTERT dilution Hi-C This paper 4DN: 4DNES9L4AK6Q HFF-hTERT clone 6 in-situ Hi-C 4D Nucleome 4DN: 4DNES2R6PUEK Rao et al in-situ Hi-C Rao et al., 2013 {"type":"entrez-geo","attrs":{"text":"GSE74072","term_id":"74072"}} GSE74072 Jin et al dilution Hi-C Jin et al., 2013 {"type":"entrez-geo","attrs":{"text":"GSE85977","term_id":"85977"}} GSE85977 FISH spot positions and distances This paper 4DN: https://data.4dnucleome.org/publications/80007b23-7748-4492-9e49-c38400acbe60/ Experimental Models: Cell Lines HFF-hTERT cells 4D Nucleome RRID: CVCL_VC40 Experimental Models: Organisms/Strains Oligonucleotides Recombinant DNA BAC clones (See Table S1 ) CHORI See Table S1 Software and Algorithms Bowtie2.2.8 Langmead and Salzberg, 2012 http://bowtie-bio.sourceforge.net/bowtie2/index.shtml Hiclib Imakaev et al., 2012 https://bitbucket.org/mirnylab/hiclib Cooler Abdennur et al, 2017 http://doi.org/10.5281/zenodo.1039971 Lavaburst (domain calling algorithms) Schwarzer et al, 2017 https://github.com/nvictus/lavaburst cWorld Lajoie et al., 2015 https://github.com/dekkerlab/cworld-dekker Other Open in a separate window HIGHLIGHTS Genome organization is highly variable between individual cells.

Techniques: Virus, Recombinant, Clone Assay, Software

(A) Genetic screen from mouse T, B and ES cells compared to yeast and the hMED minimal core. Essential subunits denoted with red boxes, non-essential with grey ones, minimal core subunits with checkmarks. (B) Bar graph shows the number of transcriptionally affected genes (>1.5 fold) in CH12 B cells deficient for non-essential (non-tail) mMED subunits. (C) Schematic showing MED14-degron strategy. A SMASh tag consisting of a linker, the hepatitis C protease, and a degron subunit was fused to MED14-N terminus. In untreated cells, the protease frees MED14 from SMASh, which is degraded. The hepatitis C protease inhibitor Asunaprevir blocks SMASh cleavage leading to MED14 degradation. (D) Transcriptome analysis of APR-treated Med14SMASh vs. control cells. Red dots represent mRNA spike-ins used to normalize signals on a per cell basis. (E) Med26, PolII, PolII-S5, PolII-S2, H3K4me3, H3K4me1, and H3K27Ac ChIP-Seq profiles at the Xbp1 locus in APR-treated WT (left) or Med14SMASh (right) cells. The orientation of genes is denoted with red arrows.

Journal: Cell

Article Title: A pliable Mediator acts as a functional rather than an architectural bridge between promoters and enhancers

doi: 10.1016/j.cell.2019.07.011

Figure Lengend Snippet: (A) Genetic screen from mouse T, B and ES cells compared to yeast and the hMED minimal core. Essential subunits denoted with red boxes, non-essential with grey ones, minimal core subunits with checkmarks. (B) Bar graph shows the number of transcriptionally affected genes (>1.5 fold) in CH12 B cells deficient for non-essential (non-tail) mMED subunits. (C) Schematic showing MED14-degron strategy. A SMASh tag consisting of a linker, the hepatitis C protease, and a degron subunit was fused to MED14-N terminus. In untreated cells, the protease frees MED14 from SMASh, which is degraded. The hepatitis C protease inhibitor Asunaprevir blocks SMASh cleavage leading to MED14 degradation. (D) Transcriptome analysis of APR-treated Med14SMASh vs. control cells. Red dots represent mRNA spike-ins used to normalize signals on a per cell basis. (E) Med26, PolII, PolII-S5, PolII-S2, H3K4me3, H3K4me1, and H3K27Ac ChIP-Seq profiles at the Xbp1 locus in APR-treated WT (left) or Med14SMASh (right) cells. The orientation of genes is denoted with red arrows.

Article Snippet: Antibody SOURCE IDENTIFIER Tested Cell Remark Med1 Bethyl A300–793A aB Not worked Med6 Origene TA343540 CH12 Not worked Med12 Bethyl A300–774A aB, CH12 Very low signal-to-noise ratio Med14 Abcam ab170605 CH12 Not worked Med14 Thermo Fisher PA5–44864 CH12 Not worked Med19 Abcam ab179735 CH12 low signal-to-noise ratio Med23 Bethyl A300–425A aB, CH12 Good quality Med24 Novus Biologicals NB100–92293 aB low signal-to-noise ratio Med25 Thermo Fisher PA5–43616 aB low signal-to-noise ratio Med26 Cell Signaling 13641S CH12 Good quality Cdk8 Abcam ab176559 CH12 low signal-to-noise ratio Open in a separate window In situ HiC We generated 34 in situ Hi-C libraries using the MboI restriction enzyme.

Techniques: Protease Inhibitor, ChIP-sequencing

Journal: Cell

Article Title: A pliable Mediator acts as a functional rather than an architectural bridge between promoters and enhancers

doi: 10.1016/j.cell.2019.07.011

Figure Lengend Snippet:

Article Snippet: Antibody SOURCE IDENTIFIER Tested Cell Remark Med1 Bethyl A300–793A aB Not worked Med6 Origene TA343540 CH12 Not worked Med12 Bethyl A300–774A aB, CH12 Very low signal-to-noise ratio Med14 Abcam ab170605 CH12 Not worked Med14 Thermo Fisher PA5–44864 CH12 Not worked Med19 Abcam ab179735 CH12 low signal-to-noise ratio Med23 Bethyl A300–425A aB, CH12 Good quality Med24 Novus Biologicals NB100–92293 aB low signal-to-noise ratio Med25 Thermo Fisher PA5–43616 aB low signal-to-noise ratio Med26 Cell Signaling 13641S CH12 Good quality Cdk8 Abcam ab176559 CH12 low signal-to-noise ratio Open in a separate window In situ HiC We generated 34 in situ Hi-C libraries using the MboI restriction enzyme.

Techniques: