cd45 1 a20 pe cy7 Search Results


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Anti Mouse Cd45.1 Pe Cy7, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible <t>in</t> <t>CD45.1</t> WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.
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Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible <t>in</t> <t>CD45.1</t> WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.
Cd45.1 Pe Cy7 A20, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible <t>in</t> <t>CD45.1</t> WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.
Anti Cd45.1 Pe.Cy7, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible <t>in</t> <t>CD45.1</t> WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.
Ter119 Pe Cy5 Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible <t>in</t> <t>CD45.1</t> WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.
Cd44 Im7 Fitc, Pe Cy7, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible <t>in</t> <t>CD45.1</t> WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.
Cd45 1, supplied by Thermo Fisher, 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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Thermo Fisher pe-cy7-cd45.1 mab
Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible <t>in</t> <t>CD45.1</t> WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.
Pe Cy7 Cd45.1 Mab, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Journal: Cell reports

Article Title: Kruppel-like factor 2+ CD4 T cells avert microbiota-induced intestinal inflammation

doi: 10.1016/j.celrep.2023.113323

Figure Lengend Snippet:

Article Snippet: PE-Cy7 anti-mouse CD45.1 (clone: A20) , eBioscience , Cat# 25-0453-82; RRID:AB_469629.

Techniques: Virus, Derivative Assay, Recombinant, Cell Stimulation, Enzyme-linked Immunosorbent Assay, Staining, Software

Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible in CD45.1 WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.

Journal: Communications Biology

Article Title: Monocytes undergo multi-step differentiation in mice during oral infection by Toxoplasma gondii

doi: 10.1038/s42003-019-0718-6

Figure Lengend Snippet: Wild type (WT)/ Stat1 −/− mixed BM chimeras were infected perorally with T. gondii cysts as depicted in Fig. . a Heatmap showing, among distal regulatory regions from clusters I and II (as defined in Fig. ), which regions were more or less accessible in CD45.1 WT and CD45.2 Stat1 −/− monocytes from the BM and the spleen of infected mice. Values are represented as log 2 fold-change obtained from the median of each single region. Bars indicate the number and the relative proportion of STAT1-dependent (in red) and -independent (in blue) regions among clusters I and II. b Representative ATAC-Seq tracks from the indicated population at the loci of Il1rn , Il27a , and Il10 . STAT1-dependent and independent peaks are highlighted in blue and green, respectively. The scale represents the fraction of reads in peaks (FRiP). c Bars indicating percentage of STAT1-dependent (in red) and -independent (in blue) regions, within clusters I and II enhancer regions overlapping with ChIP-Seq peaks of resting or LPS-stimulated BMDCs and resting and IFNγ-stimulated BMMs, for the indicated transcription factors (as shown in Fig. ). ATAC samples were generated from cells isolated from a pool of seven chimeric mice.

Article Snippet: Ly6C AL-21 BV421, CD11b M1/70 AF700, CD11c HL3 PE-Cy7, CD8α 53.6.7 PerCP, CD64 a and b alloantigens X54-5/7.1 AF647 or BV785, CD40 3/23 BV711, CD80 16-10A1 PE, CD86 GL1 APC, and CD45.1 A20 Pe-Cy7 were all purchased from BD Pharmigen as well.

Techniques: Infection, ChIP-sequencing, Generated, Isolation