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recombinant human bmp2 protein r d systems  (R&D Systems)


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    Structured Review

    R&D Systems recombinant human bmp2 protein r d systems
    Recombinant Human Bmp2 Protein R D Systems, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 224 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+human+bmp2+protein+r+d+systems/Recombinant+Human+BMP-2+GMP+Protein%2C+CF/pm41932341-856-64-68
    Average 95 stars, based on 224 article reviews
    recombinant human bmp2 protein r d systems - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Recombinant:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    Sequencing:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    RNA sequencing:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    Expressing:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    Live Cell Imaging:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    HMT Assay:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    Plasmid Preparation:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    Software:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).

    Fluorescence:

    Article Title: Single-cell morphodynamical trajectories enable prediction of gene expression accompanying cell state change.
    Article Snippet: .. Cells were maintained in DMEM/ F12 supplemented with insulin, sodium selenite, hydrocortisone, β-estrogen, and transferrin, and maintained in 5% C02 at 37◦C.111 REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, peptides, and recombinant proteins Recombinant Human EGF Protein, CF R&D Systems Cat#236-EG Recombinant Human Oncostatin M (HEK-293-expressed) Protein R&D Systems Cat#8475-OM Recombinant Human TGF-beta 1 Protein R&D Systems Cat#240-B Recombinant Human HGF Protein R&D Systems Cat#294-HG Recombinant Human BMP2 Protein R&D Systems Cat#355-BM Recombinant Human IFNу Protein R&D Systems Cat#258-IF Recombinant Human EGF Protein Peprotech Cat#AF-100-15-500UG Recombinant Human IGF Protein Peprotech Cat#100-11-500UG Recombinant Human HGF Protein Peprotech Cat#100-39H-25UG MEKi/PD0325901 Selleckchem Cat# S1036 AKTi/MK2206 Selleckchem Cat# S1078 Deposited data mcf10a maging, image analysis, sequencing data This paper https://doi.org/10.5281/zenodo.11455833 RNAseq data from combination ligand treatments Mclean et al.74 GEO: GSE282654 RNAseq and protein expression data Gross et al.65 https://synapse.org/LINCS_MCF10A Live-cell imaging from combination ligand treatments Mclean et al.74 https://doi.org/10.5281/zenodo.14261795 Experimental models: Cell lines Human: MCF10A line Gift from Gordon Mills (OHSU) N/A Human: HMT-3522 T4-2 line Gift from Mina Bissell (LBNL) N/A Recombinant DNA Plasmid: pLJM1-ERKTR-mVenus-puro Gillies et al.107 https://doi.org/10.1016/j.cels.2017.10.019 Software and algorithms DESeq2 v1.24.0 Soneson et al.108 https://bioconductor.org/packages/ release/bioc/html/DESeq2.html Label-free fluorescence prediction: pytorch_fnet Ounkomol et al.77 https://github.com/AllenCellModeling/pytorch_fnet btrack v0.4.2 Ulicna et al.78 https://github.com/quantumjot/btrack pyemma v2.5.12 Scherer et al.76 https://github.com/markovmodel/PyEMMA GSEApy Fang et al.109 https://github.com/zqfang/GSEApy CellPose v2.0 Stringer et al.110 https://github.com/MouseLand/cellpose Celltraj Copperman et al.30 https://doi.org/10.5281/zenodo.17806558 MMIST This paper https://doi.org/10.5281/zenodo.18624747 ll OPEN ACCESS Article e1 Cell Systems 17, 101567, May 20, 2026 .. Companion RNAseq and live-cell imaging data used in this paper are described in full in Gross et al.65 In brief, MCF10A cells were cultured in growth media composed of DMEM/F12 (Invitrogen #11330-032), 5% horse serum (Sigma #H1138), 20 ng/ml EGF (R&D Systems #236-EG), 10 μg/ml insulin (Sigma #I9278), 100 ng/ml cholera toxin (Sigma #C8052), 0.5 μg/ml hydrocortisone (Sigma #H4001), and 1% Pen/Strep (Invitrogen #15070-063).



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    Figure 5. Cell lines preferentially respond to different ligand combinations (A) Responses were measured for, from left to right, NMuMG cells, NMuMG cells with ACVR1 knockdown (KD), NMuMG cells with BMPR2 KD, NMuMG cells with ACVRL1 overexpression (OX), and mESCs, using flow cytometry of an integrated fluorescent protein reporter (STAR Methods: Addressing of cell lines). Each cell line was exposed to a double titration of <t>BMP2</t> and BMP9, and responses were quantified by taking the mean of at least 3 replicates. For each cell line, fold change is calculated relative to the baseline fluorescence with no added ligand and then normalized by the maximum value. Responses at select ligand words (red circles) are analyzed further in (B). (B) For select ligand words from (A), the responses of each cell line are shown. Error bars indicate SD of at least 3 repeats. Ligand words were chosen by fixing a threshold of 0.5 (gray dashed line) and identifying those ligand combinations yielding unique on- and off-target activation patterns. (C) Data from (B) are summarized by showing the response of each cell type (columns) to each ligand word (rows), illustrating that distinct ligand words can activate different subsets of cell types. (D) Responses of NMuMG, NMuMG with ACVR1 KD, and NMuMG with BMPR2 KD to BMP9 and BMP10 are shown, as in (A). (E) As in (B), the responses of each cell type at selected ligand words are shown. (F) As in (C), the responses of each cell type (columns) to each ligand word (rows) confirm that distinct ligand words preferentially activate distinct groups of cell types. See also Table S1.
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    Figure 5. Cell lines preferentially respond to different ligand combinations (A) Responses were measured for, from left to right, NMuMG cells, NMuMG cells with ACVR1 knockdown (KD), NMuMG cells with BMPR2 KD, NMuMG cells with ACVRL1 overexpression (OX), and mESCs, using flow cytometry of an integrated fluorescent protein reporter (STAR Methods: Addressing of cell lines). Each cell line was exposed to a double titration of <t>BMP2</t> and BMP9, and responses were quantified by taking the mean of at least 3 replicates. For each cell line, fold change is calculated relative to the baseline fluorescence with no added ligand and then normalized by the maximum value. Responses at select ligand words (red circles) are analyzed further in (B). (B) For select ligand words from (A), the responses of each cell line are shown. Error bars indicate SD of at least 3 repeats. Ligand words were chosen by fixing a threshold of 0.5 (gray dashed line) and identifying those ligand combinations yielding unique on- and off-target activation patterns. (C) Data from (B) are summarized by showing the response of each cell type (columns) to each ligand word (rows), illustrating that distinct ligand words can activate different subsets of cell types. (D) Responses of NMuMG, NMuMG with ACVR1 KD, and NMuMG with BMPR2 KD to BMP9 and BMP10 are shown, as in (A). (E) As in (B), the responses of each cell type at selected ligand words are shown. (F) As in (C), the responses of each cell type (columns) to each ligand word (rows) confirm that distinct ligand words preferentially activate distinct groups of cell types. See also Table S1.
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    Image Search Results


    Figure 5. Cell lines preferentially respond to different ligand combinations (A) Responses were measured for, from left to right, NMuMG cells, NMuMG cells with ACVR1 knockdown (KD), NMuMG cells with BMPR2 KD, NMuMG cells with ACVRL1 overexpression (OX), and mESCs, using flow cytometry of an integrated fluorescent protein reporter (STAR Methods: Addressing of cell lines). Each cell line was exposed to a double titration of BMP2 and BMP9, and responses were quantified by taking the mean of at least 3 replicates. For each cell line, fold change is calculated relative to the baseline fluorescence with no added ligand and then normalized by the maximum value. Responses at select ligand words (red circles) are analyzed further in (B). (B) For select ligand words from (A), the responses of each cell line are shown. Error bars indicate SD of at least 3 repeats. Ligand words were chosen by fixing a threshold of 0.5 (gray dashed line) and identifying those ligand combinations yielding unique on- and off-target activation patterns. (C) Data from (B) are summarized by showing the response of each cell type (columns) to each ligand word (rows), illustrating that distinct ligand words can activate different subsets of cell types. (D) Responses of NMuMG, NMuMG with ACVR1 KD, and NMuMG with BMPR2 KD to BMP9 and BMP10 are shown, as in (A). (E) As in (B), the responses of each cell type at selected ligand words are shown. (F) As in (C), the responses of each cell type (columns) to each ligand word (rows) confirm that distinct ligand words preferentially activate distinct groups of cell types. See also Table S1.

    Journal: Cell systems

    Article Title: Ligand-receptor promiscuity enables cellular addressing.

    doi: 10.1016/j.cels.2022.03.001

    Figure Lengend Snippet: Figure 5. Cell lines preferentially respond to different ligand combinations (A) Responses were measured for, from left to right, NMuMG cells, NMuMG cells with ACVR1 knockdown (KD), NMuMG cells with BMPR2 KD, NMuMG cells with ACVRL1 overexpression (OX), and mESCs, using flow cytometry of an integrated fluorescent protein reporter (STAR Methods: Addressing of cell lines). Each cell line was exposed to a double titration of BMP2 and BMP9, and responses were quantified by taking the mean of at least 3 replicates. For each cell line, fold change is calculated relative to the baseline fluorescence with no added ligand and then normalized by the maximum value. Responses at select ligand words (red circles) are analyzed further in (B). (B) For select ligand words from (A), the responses of each cell line are shown. Error bars indicate SD of at least 3 repeats. Ligand words were chosen by fixing a threshold of 0.5 (gray dashed line) and identifying those ligand combinations yielding unique on- and off-target activation patterns. (C) Data from (B) are summarized by showing the response of each cell type (columns) to each ligand word (rows), illustrating that distinct ligand words can activate different subsets of cell types. (D) Responses of NMuMG, NMuMG with ACVR1 KD, and NMuMG with BMPR2 KD to BMP9 and BMP10 are shown, as in (A). (E) As in (B), the responses of each cell type at selected ligand words are shown. (F) As in (C), the responses of each cell type (columns) to each ligand word (rows) confirm that distinct ligand words preferentially activate distinct groups of cell types. See also Table S1.

    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Chemicals, Peptides, and Recombinant Proteins BMP2 R&D Systems Cat# 355-BM BMP9 R&D Systems Cat# 5566-BP BMP10 R&D Systems Cat# 6038-BP Fetal Bovine Serum Clontech Cat# 631367 Fetal Bovine Serum, ES Cell Qualified Gibco Cat# 16141 Leukemia Inhibitory Factor MilliporeSigma Cat# ESG1107 Trypsin Gibco Cat# 25200 Accutase Gibco Cat# A11105 Deposited Data Optimization and simulation results This paper https://doi.org/10.22002/D1.1692 Experimental measurements of BMP responses in multiple cell lines This paper https://doi.org/10.22002/D1.1692 Experimental Models: Cell Lines NMuMG sensor line Klumpe et al., 2022 N/A NMuMG sensor line with ACVR1 knockdown Klumpe et al., 2022 N/A NMuMG sensor line with BMPR2 knockdown Klumpe et al., 2022 N/A NMuMG sensor line with ACVRL1 overexpression Klumpe et al., 2022 N/A mESC sensor line Antebi et al., 2017 N/A Software and Algorithms MATLAB MathWorks N/A Python Python Software Foundation N/A Equilibrium Toolkit (EQTK) (Python) Bois, 2020 https://github.com/justinbois/eqtk and https://doi.org/10.22002/D1.1430 PromiSys (Python) This paper https://github.com/christinasu/PromiSys and https://doi.org/10.22002/D1.20047 Simulation and analysis code (Python) This paper https://github.com/christinasu/PromiSys and https://doi.org/10.22002/D1.20047 EasyFlow (MATLAB) Antebi et al., 2017 https://github.com/AntebiLab/easyflow

    Techniques: Knockdown, Over Expression, Cytometry, Titration, Activation Assay