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R&D Systems Hematology sheep polyclonal foxc2
(A) Overlay of Mesp1 , <t>Foxc2</t> , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.
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Images

1) Product Images from "A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors"

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors

Journal: bioRxiv

doi: 10.1101/2022.08.22.504863

(A) Overlay of Mesp1 , Foxc2 , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.
Figure Legend Snippet: (A) Overlay of Mesp1 , Foxc2 , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.

Techniques Used: Gene Expression, Immunostaining, Confocal Microscopy, Control, Disruption

Related Articles

Gene Expression:

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
Article Snippet: All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.. Antibodies used in this study: sheep polyclonal Foxc2 (R&D, AF6989), chicken polyclonal GFP (Aves, GFP-1020), rabbit polyclonal Cre (Millipore, 69050).. Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).

Immunostaining:

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
Article Snippet: All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.. Antibodies used in this study: sheep polyclonal Foxc2 (R&D, AF6989), chicken polyclonal GFP (Aves, GFP-1020), rabbit polyclonal Cre (Millipore, 69050).. Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).

Confocal Microscopy:

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
Article Snippet: All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.. Antibodies used in this study: sheep polyclonal Foxc2 (R&D, AF6989), chicken polyclonal GFP (Aves, GFP-1020), rabbit polyclonal Cre (Millipore, 69050).. Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).

Control:

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
Article Snippet: All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.. Antibodies used in this study: sheep polyclonal Foxc2 (R&D, AF6989), chicken polyclonal GFP (Aves, GFP-1020), rabbit polyclonal Cre (Millipore, 69050).. Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).

Disruption:

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors
Article Snippet: All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.All steps of immunostaining protocol were done at 37°C with gentle rocking and rotation.. Antibodies used in this study: sheep polyclonal Foxc2 (R&D, AF6989), chicken polyclonal GFP (Aves, GFP-1020), rabbit polyclonal Cre (Millipore, 69050).. Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).Light sheet embryo images were acquired using Z1 Light Sheet Microscope (Zeiss) and processed as described ( ).



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Transcriptional profiles of cardiac mesoderm in Mesp1 KO embryos. (A,F,K) scRNA-seq UMAP atlases of Ai14, Smarcd3 -F6 double-positive mesoderm cells from early (A; 5504 cells), middle (F; 7666 cells) and late (K; 22,622 cells) developmental embryo stages. (B,C,G,H,L,M) Associated UMAPs colored by genotype (B,G,L) and Smarcd3 -F6-eGFP expression (C,H,M). (D,E) Early mesoderm DGE in LSMeso2 (D) and EomesPSMeso (E). (I,J) Middle mesoderm DGE in LSMeso2 (I) and Mesp1ME (J). (N-P) Late mesoderm DGE in Meso2 (N), Meso1 (O), and postLPM (P). Significant changes denoted with adjusted P <0.05. antPrSoM, anterior presomitic mesoderm; DE-ME, definitive endoderm/mesendoderm; Foxc2M, <t>Foxc2</t> + mesoderm; Meso, mesoderm; PSMeso, primitive streak mesoderm; PS-NM, primitive streak/neuromesodermal.
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(A) Overlay of Mesp1 , <t>Foxc2</t> , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.
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(A) Overlay of Mesp1 , <t>Foxc2</t> , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.
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(A) Overlay of Mesp1 , <t>Foxc2</t> , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.
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Image Search Results


Transcriptional profiles of cardiac mesoderm in Mesp1 KO embryos. (A,F,K) scRNA-seq UMAP atlases of Ai14, Smarcd3 -F6 double-positive mesoderm cells from early (A; 5504 cells), middle (F; 7666 cells) and late (K; 22,622 cells) developmental embryo stages. (B,C,G,H,L,M) Associated UMAPs colored by genotype (B,G,L) and Smarcd3 -F6-eGFP expression (C,H,M). (D,E) Early mesoderm DGE in LSMeso2 (D) and EomesPSMeso (E). (I,J) Middle mesoderm DGE in LSMeso2 (I) and Mesp1ME (J). (N-P) Late mesoderm DGE in Meso2 (N), Meso1 (O), and postLPM (P). Significant changes denoted with adjusted P <0.05. antPrSoM, anterior presomitic mesoderm; DE-ME, definitive endoderm/mesendoderm; Foxc2M, Foxc2 + mesoderm; Meso, mesoderm; PSMeso, primitive streak mesoderm; PS-NM, primitive streak/neuromesodermal.

Journal: Development (Cambridge, England)

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors

doi: 10.1242/dev.201229

Figure Lengend Snippet: Transcriptional profiles of cardiac mesoderm in Mesp1 KO embryos. (A,F,K) scRNA-seq UMAP atlases of Ai14, Smarcd3 -F6 double-positive mesoderm cells from early (A; 5504 cells), middle (F; 7666 cells) and late (K; 22,622 cells) developmental embryo stages. (B,C,G,H,L,M) Associated UMAPs colored by genotype (B,G,L) and Smarcd3 -F6-eGFP expression (C,H,M). (D,E) Early mesoderm DGE in LSMeso2 (D) and EomesPSMeso (E). (I,J) Middle mesoderm DGE in LSMeso2 (I) and Mesp1ME (J). (N-P) Late mesoderm DGE in Meso2 (N), Meso1 (O), and postLPM (P). Significant changes denoted with adjusted P <0.05. antPrSoM, anterior presomitic mesoderm; DE-ME, definitive endoderm/mesendoderm; Foxc2M, Foxc2 + mesoderm; Meso, mesoderm; PSMeso, primitive streak mesoderm; PS-NM, primitive streak/neuromesodermal.

Article Snippet: Antibodies used in this study were: sheep polyclonal Foxc2 (R&D Systems, AF6989), chicken polyclonal GFP (Aves Labs, GFP-1020), rabbit polyclonal Cre (Millipore, 69050).

Techniques: Expressing

(A) Overlay of Mesp1 , Foxc2 , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.

Journal: bioRxiv

Article Title: A Mesp1 -dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors

doi: 10.1101/2022.08.22.504863

Figure Lengend Snippet: (A) Overlay of Mesp1 , Foxc2 , and Ai14 Mesp1 -lineage gene expression in cell types of Middle mesoderm atlas UMAP. (B) Immunostaining and Light Sheet Confocal microscopy for Foxc2 (magenta), Smarcd3 -F6 (green) and Mesp1 via Cre detection (blue) in Middle stage embryos (∼E6.75). Arrowheads denote domain boundaries in control and disruption in Mesp1 KO embryo. Scale bars are 100 μm.

Article Snippet: Antibodies used in this study: sheep polyclonal Foxc2 (R&D, AF6989), chicken polyclonal GFP (Aves, GFP-1020), rabbit polyclonal Cre (Millipore, 69050).

Techniques: Gene Expression, Immunostaining, Confocal Microscopy, Control, Disruption