cd105 pe cy7 Search Results


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Thermo Fisher cd105-pe-cy7 ebioscience
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Thermo Fisher cd105-pe-cy7
a Histological section of tibial mono-cortical defects 5 days after injury, stained with Movat’s Pentachrome. The defect site is filled with soft tissue. b PCNA IHC shows active proliferation in the periosteum and defect site at this early time point. c Alkaline phosphatase staining demonstrates only a small region of osteogenic differentiation at the cortical edge. d After 14 days, the defects site is filled with woven bone, stained yellow-green with Pentachrome. e PCNA staining reveals absence of proliferation within the injury. f Alkaline phosphatase staining indicating osteogenic differentiation throughout the injury site. g Quantification of PCNA-positive cells in the injury site at POD 5 and 14. h Quantification of alkaline phosphatase staining at POD 5 and 14. i Frequency of bone-cartilage-stromal progenitor cells (BCSPs) was analyzed over the time course of fracture healing by flow cytometry using the following BCSP markers: CD45 − Ter119 − Tie2 − CD51 + CD90 − 6C3 − <t>CD105</t> + . Scale bar = 100 μm. ALP alkaline phosphatase, BCSP bone-cartilage-stromal progenitor cells, c cortical bone, PCNA proliferating cell nuclear antigen, POD postoperative day. ** p < 0.01. Data were represented as mean ± s.e.m.
Cd105 Pe Cy7, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology cd105 pe/cy7 antibody
a Histological section of tibial mono-cortical defects 5 days after injury, stained with Movat’s Pentachrome. The defect site is filled with soft tissue. b PCNA IHC shows active proliferation in the periosteum and defect site at this early time point. c Alkaline phosphatase staining demonstrates only a small region of osteogenic differentiation at the cortical edge. d After 14 days, the defects site is filled with woven bone, stained yellow-green with Pentachrome. e PCNA staining reveals absence of proliferation within the injury. f Alkaline phosphatase staining indicating osteogenic differentiation throughout the injury site. g Quantification of PCNA-positive cells in the injury site at POD 5 and 14. h Quantification of alkaline phosphatase staining at POD 5 and 14. i Frequency of bone-cartilage-stromal progenitor cells (BCSPs) was analyzed over the time course of fracture healing by flow cytometry using the following BCSP markers: CD45 − Ter119 − Tie2 − CD51 + CD90 − 6C3 − <t>CD105</t> + . Scale bar = 100 μm. ALP alkaline phosphatase, BCSP bone-cartilage-stromal progenitor cells, c cortical bone, PCNA proliferating cell nuclear antigen, POD postoperative day. ** p < 0.01. Data were represented as mean ± s.e.m.
Cd105 Pe/Cy7 Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher scientific25 1057 42
Antibody panel created for the study.
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Thermo Fisher cd105 pe cy7
Antibody panel created for the study.
Cd105 Pe Cy7, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher alexa 647 anti-sca1
Antibody panel created for the study.
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Thermo Fisher cd90-apc antibody
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Danaher Inc cd105 pe cy7
Antibody panel created for the study.
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Thermo Fisher anti mouse cd105 pe cy7
Antibody panel created for the study.
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Becton Dickinson cd105-bv786
Antibody panel created for the study.
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Becton Dickinson cd106-v450
Antibody panel created for the study.
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Thermo Fisher anti-mouse cd105 mj7/18; pe
Antibody panel created for the study.
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Image Search Results


a Histological section of tibial mono-cortical defects 5 days after injury, stained with Movat’s Pentachrome. The defect site is filled with soft tissue. b PCNA IHC shows active proliferation in the periosteum and defect site at this early time point. c Alkaline phosphatase staining demonstrates only a small region of osteogenic differentiation at the cortical edge. d After 14 days, the defects site is filled with woven bone, stained yellow-green with Pentachrome. e PCNA staining reveals absence of proliferation within the injury. f Alkaline phosphatase staining indicating osteogenic differentiation throughout the injury site. g Quantification of PCNA-positive cells in the injury site at POD 5 and 14. h Quantification of alkaline phosphatase staining at POD 5 and 14. i Frequency of bone-cartilage-stromal progenitor cells (BCSPs) was analyzed over the time course of fracture healing by flow cytometry using the following BCSP markers: CD45 − Ter119 − Tie2 − CD51 + CD90 − 6C3 − CD105 + . Scale bar = 100 μm. ALP alkaline phosphatase, BCSP bone-cartilage-stromal progenitor cells, c cortical bone, PCNA proliferating cell nuclear antigen, POD postoperative day. ** p < 0.01. Data were represented as mean ± s.e.m.

Journal: NPJ Regenerative Medicine

Article Title: Notch-Wnt signal crosstalk regulates proliferation and differentiation of osteoprogenitor cells during intramembranous bone healing

doi: 10.1038/s41536-021-00139-x

Figure Lengend Snippet: a Histological section of tibial mono-cortical defects 5 days after injury, stained with Movat’s Pentachrome. The defect site is filled with soft tissue. b PCNA IHC shows active proliferation in the periosteum and defect site at this early time point. c Alkaline phosphatase staining demonstrates only a small region of osteogenic differentiation at the cortical edge. d After 14 days, the defects site is filled with woven bone, stained yellow-green with Pentachrome. e PCNA staining reveals absence of proliferation within the injury. f Alkaline phosphatase staining indicating osteogenic differentiation throughout the injury site. g Quantification of PCNA-positive cells in the injury site at POD 5 and 14. h Quantification of alkaline phosphatase staining at POD 5 and 14. i Frequency of bone-cartilage-stromal progenitor cells (BCSPs) was analyzed over the time course of fracture healing by flow cytometry using the following BCSP markers: CD45 − Ter119 − Tie2 − CD51 + CD90 − 6C3 − CD105 + . Scale bar = 100 μm. ALP alkaline phosphatase, BCSP bone-cartilage-stromal progenitor cells, c cortical bone, PCNA proliferating cell nuclear antigen, POD postoperative day. ** p < 0.01. Data were represented as mean ± s.e.m.

Article Snippet: CD105-PE-Cy7 , Thermo Fisher Scientific , 1:200.

Techniques: Staining, Flow Cytometry

Antibodies for flow cytometry.

Journal: NPJ Regenerative Medicine

Article Title: Notch-Wnt signal crosstalk regulates proliferation and differentiation of osteoprogenitor cells during intramembranous bone healing

doi: 10.1038/s41536-021-00139-x

Figure Lengend Snippet: Antibodies for flow cytometry.

Article Snippet: CD105-PE-Cy7 , Thermo Fisher Scientific , 1:200.

Techniques: Cytometry

Antibody panel created for the study.

Journal: International Journal of Molecular Sciences

Article Title: The Expression Pattern of Surface Markers in Canine Adipose-Derived Mesenchymal Stem Cells

doi: 10.3390/ijms22147476

Figure Lengend Snippet: Antibody panel created for the study.

Article Snippet: CD105 , SN6 , Mouse , PE-Cy 7 , Human, published species canine , Monoclonal , Thermo Fisher Scientific25-1057-42.

Techniques: