early passage molm 13 cells Search Results


early passage molm 13 cells  (DSMZ)
97
DSMZ early passage molm 13 cells
Early Passage Molm 13 Cells, supplied by DSMZ, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/early+passage+molm+13+cells/pmc10544224-130-0-3?v=DSMZ
Average 97 stars, based on 1 article reviews
early passage molm 13 cells - by Bioz Stars, 2026-08
97/100 stars
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molm1  (DSMZ)
93
DSMZ molm1
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Molm1, supplied by DSMZ, 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/early+passage+molm+13+cells/pmc11095456-161-0-4?v=DSMZ
Average 93 stars, based on 1 article reviews
molm1 - by Bioz Stars, 2026-08
93/100 stars
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ccrf-cem  (CEM Corporation)
90
CEM Corporation ccrf-cem
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Ccrf Cem, supplied by CEM Corporation, 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/early+passage+molm+13+cells/pm37741966-145-22-24?v=CEM+Corporation
Average 90 stars, based on 1 article reviews
ccrf-cem - by Bioz Stars, 2026-08
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apoa1 apolipoprotein  (Mole AS)
90
Mole AS apoa1 apolipoprotein
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Apoa1 Apolipoprotein, supplied by Mole AS, 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/early+passage+molm+13+cells/pm28031419-55-23-20?v=Mole+AS
Average 90 stars, based on 1 article reviews
apoa1 apolipoprotein - by Bioz Stars, 2026-08
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chemsketch software 2021  (ACD Labs Inc)
90
ACD Labs Inc chemsketch software 2021
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Chemsketch Software 2021, supplied by ACD Labs 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/early+passage+molm+13+cells/pmc10961656-121-10-22?v=ACD+Labs+Inc
Average 90 stars, based on 1 article reviews
chemsketch software 2021 - by Bioz Stars, 2026-08
90/100 stars
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molm-13  (AddexBio Inc)
90
AddexBio Inc molm-13
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Molm 13, supplied by AddexBio 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/early+passage+molm+13+cells/pmc06691696-28-0-4?v=AddexBio+Inc
Average 90 stars, based on 1 article reviews
molm-13 - by Bioz Stars, 2026-08
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powerplex21 pcr kit  (Promega)
90
Promega powerplex21 pcr kit
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Powerplex21 Pcr Kit, 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/early+passage+molm+13+cells/bio_rxiv__2023__12__18__572101-346-1-12?v=Promega
Average 90 stars, based on 1 article reviews
powerplex21 pcr kit - by Bioz Stars, 2026-08
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molm  (Procell Inc)
86
Procell Inc molm
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Molm, supplied by Procell 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/early+passage+molm+13+cells/pm41760705-39-17-21?v=Procell+Inc
Average 86 stars, based on 1 article reviews
molm - by Bioz Stars, 2026-08
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molm-14  (Johns Hopkins HealthCare)
90
Johns Hopkins HealthCare molm-14
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Molm 14, supplied by Johns Hopkins HealthCare, 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/early+passage+molm+13+cells/us09873743-2223-2-14?v=Johns+Hopkins+HealthCare
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lucif-erase-introduced molm-13  (FUJIFILM)
90
FUJIFILM lucif-erase-introduced molm-13
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Lucif Erase Introduced Molm 13, supplied by FUJIFILM, 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/early+passage+molm+13+cells/pmc10985452-41-1-6?v=FUJIFILM
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molm-13 cells  (CLS Cell Lines Service GmbH)
90
CLS Cell Lines Service GmbH molm-13 cells
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Molm 13 Cells, supplied by CLS Cell Lines Service 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/early+passage+molm+13+cells/custom%40305393%40pmc10656288__41565_2023_1471_MOESM1_ESM?v=CLS+Cell+Lines+Service+GmbH
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molm-13 cells - by Bioz Stars, 2026-08
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molm-13 (acc 554)  (Biochrom)
90
Biochrom molm-13 (acc 554)
( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in <t>MOLM1</t> cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).
Molm 13 (Acc 554), supplied by Biochrom, 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/early+passage+molm+13+cells/pmc04648523-24-9-19?v=Biochrom
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molm-13 (acc 554) - by Bioz Stars, 2026-08
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Image Search Results


( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in MOLM1 cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).

Journal: Science Advances

Article Title: Oncogene EVI1 drives acute myeloid leukemia via a targetable interaction with CTBP2

doi: 10.1126/sciadv.adk9076

Figure Lengend Snippet: ( A ) Differential enrichment of proteins binding to EVI1 as determined by an EVI1 specific IP compared to a nonspecific IgG IP followed by MS in MUTZ3 nuclear protein extracts ( n = 3 for each group, thresholds log 2 FC > 1 and P value < 0.05). FC, fold change. Top 4 enriched gene identifiers are highlighted in red [MECOM (EVI1), CTBP1, and CTBP2]. In addition, several previously identified MECOM interactors are shown in gray (BioGrid). ( B ) Network plot of protein complex enrichment analysis of the proteins coprecipitated with EVI1 IP in MUTZ3 cells. The connections (edges) between proteins (nodes) were weighted on the basis of their co-occurrence in CORUM complexes. Node color represents the cluster assigned to a protein; dot size represents the fold enrichment in the IP. Font size of CTBP1 and CTBP2 was adjusted manually, and colored areas and their corresponding labels were added manually based on the common biochemical functions. The full plot with all labels is presented in fig. S1C. ( C ) Heatmaps of ChIP-seq experiments in MUTZ3 cells using antibodies directed to the indicated transcription factors or histone modifications. Ranking was based on the ChIP-seq EVI1 signal (leftmost panel) showing signal intensity of indicated ChIP-seq tracks in a ± 1000-bp region centered on EVI1 peaks (21505 peaks). ( D ) Quantification of the heatmap in (C). Normalized EVI1 signal is plotted versus the normalized reads in the indicated ChIP-seq tracks for all EVI1 peaks with a window of ±1000 bp. Correlation coefficients and linear regression equations are shown for log 10 -transformed data with a pseudo count of 1. ( E ) Heatmap of CTBP2 ChIP-seq data following dox-inducible short hairpin RNA–mediated knockdown of EVI1 (48 hours) in MOLM1 cells. On the right, EVI1 heatmap in unperturbed MOLM1 cells. Tracks are ranked on peaks in the CTBP2 control track (leftmost panel, 64,569 peaks).

Article Snippet: MOLM1, HNT34, and HL60 (DSMZ, catalog no. ACC720, ACC600, and ACC3) were cultured in RPMI and 10% FCS.

Techniques: Binding Assay, ChIP-sequencing, Transformation Assay, shRNA, Knockdown, Control