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Expression of COL5A2, <t>COL1A2,</t> PRRX1, and TGFβ2 was detected in the periosteal region and the primary ossification centers. A. Merged and single-channel images of COL5A2 (red) and DAPI (blue) staining. B. Merged and single-channel images of <t>COL1A2</t> (red) and DAPI (blue) staining. C. Merged and single-channel images of PRRX1 (red) and DAPI (blue) staining. D. Merged and single-channel images of TGFβ2 (red) and DAPI (blue) staining. All experiments were independently repeated at least three times. Scale bars in snapshot image, 200 μm; scale bars in magnified images, 50 μm.
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( A ) Uniform Manifold Approximation and Projection (UMAP) clustering of 434,810 cells from eight public scRNA-seq datasets. ( B ) Dot plot showing relative Cdh5 and Runx1 co-expression across clusters; clusters 8 and 50 co-express both genes. ( C ) UMAP highlighting clusters 8 and 50; all other clusters shown in grey. ( D ) Violin plots of doublet scores across Leiden clusters. Clusters 50 and 8 show no evidence of doublet enrichment. ( E ) Datasets proportional contribution to clusters 50 and 8; each dataset is color-coded. ( F ) Dot plot showing expression of selected marker genes in clusters 50 and 8 (from the public sc RNA-seq datasets listed in ) and from clusters 0, 1, 13, 22, and 14 (from Polylox scRNA-seq; ). Results reflect mean expression and fraction of cells in group. ( G ) Cdh5, Runx1, and <t>Col1a2</t> co-expression in the indicated clusters as a fraction of cells in the cluster. ( H, I ) t-SNE plot of ECs from 11 murine tissues ( G ) and Venn diagram ( H ) showing rare co-expression of Cdh5, Runx1, and Col1a2 in these tissues.
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( A ) Uniform Manifold Approximation and Projection (UMAP) clustering of 434,810 cells from eight public scRNA-seq datasets. ( B ) Dot plot showing relative Cdh5 and Runx1 co-expression across clusters; clusters 8 and 50 co-express both genes. ( C ) UMAP highlighting clusters 8 and 50; all other clusters shown in grey. ( D ) Violin plots of doublet scores across Leiden clusters. Clusters 50 and 8 show no evidence of doublet enrichment. ( E ) Datasets proportional contribution to clusters 50 and 8; each dataset is color-coded. ( F ) Dot plot showing expression of selected marker genes in clusters 50 and 8 (from the public sc RNA-seq datasets listed in ) and from clusters 0, 1, 13, 22, and 14 (from Polylox scRNA-seq; ). Results reflect mean expression and fraction of cells in group. ( G ) Cdh5, Runx1, and <t>Col1a2</t> co-expression in the indicated clusters as a fraction of cells in the cluster. ( H, I ) t-SNE plot of ECs from 11 murine tissues ( G ) and Venn diagram ( H ) showing rare co-expression of Cdh5, Runx1, and Col1a2 in these tissues.
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( A ) Uniform Manifold Approximation and Projection (UMAP) clustering of 434,810 cells from eight public scRNA-seq datasets. ( B ) Dot plot showing relative Cdh5 and Runx1 co-expression across clusters; clusters 8 and 50 co-express both genes. ( C ) UMAP highlighting clusters 8 and 50; all other clusters shown in grey. ( D ) Violin plots of doublet scores across Leiden clusters. Clusters 50 and 8 show no evidence of doublet enrichment. ( E ) Datasets proportional contribution to clusters 50 and 8; each dataset is color-coded. ( F ) Dot plot showing expression of selected marker genes in clusters 50 and 8 (from the public sc RNA-seq datasets listed in ) and from clusters 0, 1, 13, 22, and 14 (from Polylox scRNA-seq; ). Results reflect mean expression and fraction of cells in group. ( G ) Cdh5, Runx1, and <t>Col1a2</t> co-expression in the indicated clusters as a fraction of cells in the cluster. ( H, I ) t-SNE plot of ECs from 11 murine tissues ( G ) and Venn diagram ( H ) showing rare co-expression of Cdh5, Runx1, and Col1a2 in these tissues.
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( A ) Uniform Manifold Approximation and Projection (UMAP) clustering of 434,810 cells from eight public scRNA-seq datasets. ( B ) Dot plot showing relative Cdh5 and Runx1 co-expression across clusters; clusters 8 and 50 co-express both genes. ( C ) UMAP highlighting clusters 8 and 50; all other clusters shown in grey. ( D ) Violin plots of doublet scores across Leiden clusters. Clusters 50 and 8 show no evidence of doublet enrichment. ( E ) Datasets proportional contribution to clusters 50 and 8; each dataset is color-coded. ( F ) Dot plot showing expression of selected marker genes in clusters 50 and 8 (from the public sc RNA-seq datasets listed in ) and from clusters 0, 1, 13, 22, and 14 (from Polylox scRNA-seq; ). Results reflect mean expression and fraction of cells in group. ( G ) Cdh5, Runx1, and <t>Col1a2</t> co-expression in the indicated clusters as a fraction of cells in the cluster. ( H, I ) t-SNE plot of ECs from 11 murine tissues ( G ) and Venn diagram ( H ) showing rare co-expression of Cdh5, Runx1, and Col1a2 in these tissues.
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Image Search Results


Journal: Cell Reports Medicine

Article Title: A biomimetic hybrid membrane vesicle nanoplatform attenuates tendinopathy through neuroinflammation modulation and tendon regeneration

doi: 10.1016/j.xcrm.2026.102937

Figure Lengend Snippet:

Article Snippet: Rabbit Polyclonal anti-COL1A2 , ABclonal , Cat# A21059; RRID: AB_3712537.

Techniques: Recombinant, Lysis, Hydroxyproline Assay, Enzyme-linked Immunosorbent Assay, Isolation, SYBR Green Assay, Bicinchoninic Acid Protein Assay, Staining, Software

Expression of COL5A2, COL1A2, PRRX1, and TGFβ2 was detected in the periosteal region and the primary ossification centers. A. Merged and single-channel images of COL5A2 (red) and DAPI (blue) staining. B. Merged and single-channel images of COL1A2 (red) and DAPI (blue) staining. C. Merged and single-channel images of PRRX1 (red) and DAPI (blue) staining. D. Merged and single-channel images of TGFβ2 (red) and DAPI (blue) staining. All experiments were independently repeated at least three times. Scale bars in snapshot image, 200 μm; scale bars in magnified images, 50 μm.

Journal: PLOS One

Article Title: Single-cell profiling unveils key regulators of skeletal stem cells in chicken and human embryonic limb development

doi: 10.1371/journal.pone.0346514

Figure Lengend Snippet: Expression of COL5A2, COL1A2, PRRX1, and TGFβ2 was detected in the periosteal region and the primary ossification centers. A. Merged and single-channel images of COL5A2 (red) and DAPI (blue) staining. B. Merged and single-channel images of COL1A2 (red) and DAPI (blue) staining. C. Merged and single-channel images of PRRX1 (red) and DAPI (blue) staining. D. Merged and single-channel images of TGFβ2 (red) and DAPI (blue) staining. All experiments were independently repeated at least three times. Scale bars in snapshot image, 200 μm; scale bars in magnified images, 50 μm.

Article Snippet: The following antibodies were used: anti-COL5A2 antibody ( GB111012 , 1:500, Servicebio, Wuhan, China), anti-COL1A2 antibody (AF7001, 1:200, Affinity Biosciences, Jiangsu, China), anti-PRRX1 antibody (DF4274, 1:200, Affinity Biosciences, Jiangsu, China), anti-TGFβ2 antibody (AF0260, 1:100, Affinity Biosciences, Jiangsu, China), and Cy3-conjugated goat anti-rabbit IgG (GB21303, 1:300, Servicebio, Wuhan, China).

Techniques: Expressing, Staining

( A ) Uniform Manifold Approximation and Projection (UMAP) clustering of 434,810 cells from eight public scRNA-seq datasets. ( B ) Dot plot showing relative Cdh5 and Runx1 co-expression across clusters; clusters 8 and 50 co-express both genes. ( C ) UMAP highlighting clusters 8 and 50; all other clusters shown in grey. ( D ) Violin plots of doublet scores across Leiden clusters. Clusters 50 and 8 show no evidence of doublet enrichment. ( E ) Datasets proportional contribution to clusters 50 and 8; each dataset is color-coded. ( F ) Dot plot showing expression of selected marker genes in clusters 50 and 8 (from the public sc RNA-seq datasets listed in ) and from clusters 0, 1, 13, 22, and 14 (from Polylox scRNA-seq; ). Results reflect mean expression and fraction of cells in group. ( G ) Cdh5, Runx1, and Col1a2 co-expression in the indicated clusters as a fraction of cells in the cluster. ( H, I ) t-SNE plot of ECs from 11 murine tissues ( G ) and Venn diagram ( H ) showing rare co-expression of Cdh5, Runx1, and Col1a2 in these tissues.

Journal: eLife

Article Title: Single-cell lineage tracing identifies hemogenic endothelial cells in the adult mouse bone marrow

doi: 10.7554/eLife.109553

Figure Lengend Snippet: ( A ) Uniform Manifold Approximation and Projection (UMAP) clustering of 434,810 cells from eight public scRNA-seq datasets. ( B ) Dot plot showing relative Cdh5 and Runx1 co-expression across clusters; clusters 8 and 50 co-express both genes. ( C ) UMAP highlighting clusters 8 and 50; all other clusters shown in grey. ( D ) Violin plots of doublet scores across Leiden clusters. Clusters 50 and 8 show no evidence of doublet enrichment. ( E ) Datasets proportional contribution to clusters 50 and 8; each dataset is color-coded. ( F ) Dot plot showing expression of selected marker genes in clusters 50 and 8 (from the public sc RNA-seq datasets listed in ) and from clusters 0, 1, 13, 22, and 14 (from Polylox scRNA-seq; ). Results reflect mean expression and fraction of cells in group. ( G ) Cdh5, Runx1, and Col1a2 co-expression in the indicated clusters as a fraction of cells in the cluster. ( H, I ) t-SNE plot of ECs from 11 murine tissues ( G ) and Venn diagram ( H ) showing rare co-expression of Cdh5, Runx1, and Col1a2 in these tissues.

Article Snippet: TaqMan probes used were purchased from Applied Biosystems: Spp1 (Mm00436767_m1); Cxcl12 (Mm00445553_m1); Col1a2 (Mm00483888_m1); Cdh5 (Mm00486938_m1); Runx1 (Mm01213404_m1); Ptprc (Mm01293577_m1); Gapdh (Mm99999915_g1); Actb (Mm02619580_g1).

Techniques: Expressing, Marker, RNA Sequencing

Related to . ( A ) Schematic representation of the Col1a2 tracking lines. ( B ) Representative confocal image of a BM section from a tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen mouse, showing widespread distribution of ZsGreen + cells. Flow cytometric identification of RUNX1 + VE-Cadherin + CD45 − endothelial cells (ECs) in the BM of peanut oil-treated ( n = 6) and tamoxifen-treated ( n = 6) Col1a2-Cre ERT2 /ZsGreen adult mice; Cre − mice ( n = 5) ( C ); WT C57Bl/6 mice ( n = 6) and Fluorescence Minus One (FMO) control ( n = 5) ( D ); and Cdh5-Cre ERT2 (PAC)/ZsGreen mice treated with peanut oil ( n = 6) or tamoxifen ( n = 6); Cre − mice ( n = 5) ( E ). Left panels: quantification of cells identified by the indicated gates as a percentage of total BM ECs; each dot represents one mouse (1 femur + 1 tibia). Middle and right panels: representative gating strategies. ( F ) Representative confocal microscopy image of a BM section from a tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen adult mouse showing a ZsGreen + Endomucin + cell lining a vascular structure (white arrows). ( G ) Representative confocal image of a blood smear from a Col1a2-Cre ERT2 /ZsGreen mouse treated with tamoxifen showing the presence of a nucleate CD45 + cell tracked by ZsGreen/Col1a2 fluorescence (pointed by the arrow). ( H ) Representative confocal image of a blood smear from a Col1a2-Cre ERT2 /mTmG mouse treated with tamoxifen showing the presence of a nucleated CD45 + cell tracked by EGFP/Col1a2 fluorescence (pointed by the arrow). Dots represent individual mice. Data are shown as mean ± SD. ***p < 0.001 by Student’s t -test.

Journal: eLife

Article Title: Single-cell lineage tracing identifies hemogenic endothelial cells in the adult mouse bone marrow

doi: 10.7554/eLife.109553

Figure Lengend Snippet: Related to . ( A ) Schematic representation of the Col1a2 tracking lines. ( B ) Representative confocal image of a BM section from a tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen mouse, showing widespread distribution of ZsGreen + cells. Flow cytometric identification of RUNX1 + VE-Cadherin + CD45 − endothelial cells (ECs) in the BM of peanut oil-treated ( n = 6) and tamoxifen-treated ( n = 6) Col1a2-Cre ERT2 /ZsGreen adult mice; Cre − mice ( n = 5) ( C ); WT C57Bl/6 mice ( n = 6) and Fluorescence Minus One (FMO) control ( n = 5) ( D ); and Cdh5-Cre ERT2 (PAC)/ZsGreen mice treated with peanut oil ( n = 6) or tamoxifen ( n = 6); Cre − mice ( n = 5) ( E ). Left panels: quantification of cells identified by the indicated gates as a percentage of total BM ECs; each dot represents one mouse (1 femur + 1 tibia). Middle and right panels: representative gating strategies. ( F ) Representative confocal microscopy image of a BM section from a tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen adult mouse showing a ZsGreen + Endomucin + cell lining a vascular structure (white arrows). ( G ) Representative confocal image of a blood smear from a Col1a2-Cre ERT2 /ZsGreen mouse treated with tamoxifen showing the presence of a nucleate CD45 + cell tracked by ZsGreen/Col1a2 fluorescence (pointed by the arrow). ( H ) Representative confocal image of a blood smear from a Col1a2-Cre ERT2 /mTmG mouse treated with tamoxifen showing the presence of a nucleated CD45 + cell tracked by EGFP/Col1a2 fluorescence (pointed by the arrow). Dots represent individual mice. Data are shown as mean ± SD. ***p < 0.001 by Student’s t -test.

Article Snippet: TaqMan probes used were purchased from Applied Biosystems: Spp1 (Mm00436767_m1); Cxcl12 (Mm00445553_m1); Col1a2 (Mm00483888_m1); Cdh5 (Mm00486938_m1); Runx1 (Mm01213404_m1); Ptprc (Mm01293577_m1); Gapdh (Mm99999915_g1); Actb (Mm02619580_g1).

Techniques: Fluorescence, Control, Confocal Microscopy

Percent EGFP + CD45 + cells in bone marrow (BM) and blood of tamoxifen-treated ( n = 6) or oil-treated ( n = 5) Col1a2-Cre ERT2 /mTmG mice ( A ) and tamoxifen-treated ( n = 4) or oil-treated ( n = 3) Col1a2-Cre ERT2 /ZsGreen mice ( B ). Cre-control mice ( n = 5 in A, and n = 2 in B). ( C ) Transplant experiment: sorted VE-Cadherin + CD45 − ZsGreen + /Col1a2 + cells from tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen mice are transplanted into 5-FU-conditioned WT recipients. Detection ( D ) and characterization ( E ) of ZsGreen + CD45 + cells in BM and blood of WT 5-FU-conditioned mice ( n = 5), 4 weeks post-transplant of VE-Cadherin + CD45⁻ZsGreen + /Col1a2 + cells. Control FU-conditioned WT mice ( n = 4) received no cell transplant ( D ). ( F ) Time course of ZsGreen + peripheral blood mononuclear cell (PBMC) detection in control (Cdh5-Cre + /ZsGreen + ) and Runx1 EC-KI (Cdh5-Cre + /ZsGreen + /Runx1-KI) mice ( n = 10 per group). Representative images ( G ) and quantification ( H ) of ZsGreen + cells from OP9 cell-supported cultures of BM cells from tamoxifen-treated Cdh5-Cre + /ZsGreen + ( n = 11) and Runx1 EC-KI mice ( n = 5). Representative flow cytometry plots ( I ) and quantification ( J ) of CD45 + ZsGreen + cells from OP9 cell-supported BM cell cultures ( n = 5/group). Dots represent individual mice. Data are shown as mean ± SD. **p < 0.01, ***p < 0.001 by Student’s t -test.

Journal: eLife

Article Title: Single-cell lineage tracing identifies hemogenic endothelial cells in the adult mouse bone marrow

doi: 10.7554/eLife.109553

Figure Lengend Snippet: Percent EGFP + CD45 + cells in bone marrow (BM) and blood of tamoxifen-treated ( n = 6) or oil-treated ( n = 5) Col1a2-Cre ERT2 /mTmG mice ( A ) and tamoxifen-treated ( n = 4) or oil-treated ( n = 3) Col1a2-Cre ERT2 /ZsGreen mice ( B ). Cre-control mice ( n = 5 in A, and n = 2 in B). ( C ) Transplant experiment: sorted VE-Cadherin + CD45 − ZsGreen + /Col1a2 + cells from tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen mice are transplanted into 5-FU-conditioned WT recipients. Detection ( D ) and characterization ( E ) of ZsGreen + CD45 + cells in BM and blood of WT 5-FU-conditioned mice ( n = 5), 4 weeks post-transplant of VE-Cadherin + CD45⁻ZsGreen + /Col1a2 + cells. Control FU-conditioned WT mice ( n = 4) received no cell transplant ( D ). ( F ) Time course of ZsGreen + peripheral blood mononuclear cell (PBMC) detection in control (Cdh5-Cre + /ZsGreen + ) and Runx1 EC-KI (Cdh5-Cre + /ZsGreen + /Runx1-KI) mice ( n = 10 per group). Representative images ( G ) and quantification ( H ) of ZsGreen + cells from OP9 cell-supported cultures of BM cells from tamoxifen-treated Cdh5-Cre + /ZsGreen + ( n = 11) and Runx1 EC-KI mice ( n = 5). Representative flow cytometry plots ( I ) and quantification ( J ) of CD45 + ZsGreen + cells from OP9 cell-supported BM cell cultures ( n = 5/group). Dots represent individual mice. Data are shown as mean ± SD. **p < 0.01, ***p < 0.001 by Student’s t -test.

Article Snippet: TaqMan probes used were purchased from Applied Biosystems: Spp1 (Mm00436767_m1); Cxcl12 (Mm00445553_m1); Col1a2 (Mm00483888_m1); Cdh5 (Mm00486938_m1); Runx1 (Mm01213404_m1); Ptprc (Mm01293577_m1); Gapdh (Mm99999915_g1); Actb (Mm02619580_g1).

Techniques: Control, Flow Cytometry

Related to . ( A ) Representative FACS gating strategy used to isolate BM hematopoietic cells, ECs, stromal cells, and Col1a2-tracked ECs from tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen mice. ( B ) Gene expression profiling of unsorted BM and sorted BM populations defined in ( A ). Results from qRT-PCR are normalized by Gapdh and unsorted BM. Dots reflect experimental triplicates. ( C ) Representative confocal image of a BM section from a transplant recipient showing a CD45 + CD11b + ZsGreen + cell (arrow), indicating hematopoietic derivation from transplanted ZsGreen + VE-Cadherin + CD45 − (Col1a2 + ) cells. ( D ) Representative image of a blood smear from a WT recipient mouse transplanted with ZsGreen (Col1a2) + BM ECs from Col1a2-Cre ERT2 /ZsGreen mice. ZsGreen tracked cells are pointed by the arrows. ( E ) Schematic diagram of the Cdh5-Cre ERT2 /ZsGreen/Runx1-Knock-in (Runx1 EC-KI ) mouse line used to trace ECs with Runx1 expression induced upon tamoxifen treatment.

Journal: eLife

Article Title: Single-cell lineage tracing identifies hemogenic endothelial cells in the adult mouse bone marrow

doi: 10.7554/eLife.109553

Figure Lengend Snippet: Related to . ( A ) Representative FACS gating strategy used to isolate BM hematopoietic cells, ECs, stromal cells, and Col1a2-tracked ECs from tamoxifen-treated Col1a2-Cre ERT2 /ZsGreen mice. ( B ) Gene expression profiling of unsorted BM and sorted BM populations defined in ( A ). Results from qRT-PCR are normalized by Gapdh and unsorted BM. Dots reflect experimental triplicates. ( C ) Representative confocal image of a BM section from a transplant recipient showing a CD45 + CD11b + ZsGreen + cell (arrow), indicating hematopoietic derivation from transplanted ZsGreen + VE-Cadherin + CD45 − (Col1a2 + ) cells. ( D ) Representative image of a blood smear from a WT recipient mouse transplanted with ZsGreen (Col1a2) + BM ECs from Col1a2-Cre ERT2 /ZsGreen mice. ZsGreen tracked cells are pointed by the arrows. ( E ) Schematic diagram of the Cdh5-Cre ERT2 /ZsGreen/Runx1-Knock-in (Runx1 EC-KI ) mouse line used to trace ECs with Runx1 expression induced upon tamoxifen treatment.

Article Snippet: TaqMan probes used were purchased from Applied Biosystems: Spp1 (Mm00436767_m1); Cxcl12 (Mm00445553_m1); Col1a2 (Mm00483888_m1); Cdh5 (Mm00486938_m1); Runx1 (Mm01213404_m1); Ptprc (Mm01293577_m1); Gapdh (Mm99999915_g1); Actb (Mm02619580_g1).

Techniques: Gene Expression, Quantitative RT-PCR, Knock-In, Expressing