ma900 high resolution flow cytometer Search Results


sony ma900 flow cytometer  (Sony Biotechnology)
99
Sony Biotechnology sony ma900 flow cytometer
Sony Ma900 Flow Cytometer, supplied by Sony Biotechnology, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ma900+high+resolution+flow+cytometer/pmc12866971-74-6-6?v=Sony+Biotechnology
Average 99 stars, based on 1 article reviews
sony ma900 flow cytometer - by Bioz Stars, 2026-07
99/100 stars
  Buy from Supplier
flow cytometer ma900  (Sony)
90
Sony flow cytometer ma900
Angiogenic potential of muse cells. (A) Representative images showing vascular endothelial markers CD31 expression of mCherry-expressing Muse cells in the ischemic adductor muscles at 7 days after hindlimb ischemia (HLI) surgery. Tissue sections were stained with anti-CD31 antibody (green) and 4′6-diamidino-2-phenylindole (DAPI) (blue). Scale bar, 50 μm. (B) Flow <t>cytometric</t> analysis of CD31 expression in the ischemic adductor muscles at 7 days after HLI surgery ( n = 5). Results are expressed as mean ± SEM of the percentage of mCherry/CD31 double-positive cells per total CD31-positive cell count in the dissociated ischemic adductor muscle. Dots correspond to each mouse. (C) Vascular endothelial growth factor (VEGF) concentration measured by enzyme-linked immunosorbent assay (ELISA) in the cell culture supernatant of Muse cells or non-Muse mesenchymal stem cells (MSCs) under normoxic and hypoxic conditions. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each biological replicate. (D,E) VEGF concentration measured by ELISA in the adductor muscles (D) and relative mRNA expression of representative angiogenic factors in the ischemic adductor muscle (E) at 7 days after HLI surgery. Muse cells or non-Muse MSCs were intravenously injected 1 day after HLI surgery and phosphate buffered saline was injected as a control. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each mouse. * P < 0.05; ** P < 0.01.
Flow Cytometer Ma900, supplied by Sony, 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/ma900+high+resolution+flow+cytometer/pmc09692087-54-16-19?v=Sony
Average 90 stars, based on 1 article reviews
flow cytometer ma900 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
flow cytometers  (Sony Biotechnology)
99
Sony Biotechnology flow cytometers
Angiogenic potential of muse cells. (A) Representative images showing vascular endothelial markers CD31 expression of mCherry-expressing Muse cells in the ischemic adductor muscles at 7 days after hindlimb ischemia (HLI) surgery. Tissue sections were stained with anti-CD31 antibody (green) and 4′6-diamidino-2-phenylindole (DAPI) (blue). Scale bar, 50 μm. (B) Flow <t>cytometric</t> analysis of CD31 expression in the ischemic adductor muscles at 7 days after HLI surgery ( n = 5). Results are expressed as mean ± SEM of the percentage of mCherry/CD31 double-positive cells per total CD31-positive cell count in the dissociated ischemic adductor muscle. Dots correspond to each mouse. (C) Vascular endothelial growth factor (VEGF) concentration measured by enzyme-linked immunosorbent assay (ELISA) in the cell culture supernatant of Muse cells or non-Muse mesenchymal stem cells (MSCs) under normoxic and hypoxic conditions. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each biological replicate. (D,E) VEGF concentration measured by ELISA in the adductor muscles (D) and relative mRNA expression of representative angiogenic factors in the ischemic adductor muscle (E) at 7 days after HLI surgery. Muse cells or non-Muse MSCs were intravenously injected 1 day after HLI surgery and phosphate buffered saline was injected as a control. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each mouse. * P < 0.05; ** P < 0.01.
Flow Cytometers, supplied by Sony Biotechnology, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ma900+high+resolution+flow+cytometer/pmc12365847__mmc1-44-8-13?v=Sony+Biotechnology
Average 99 stars, based on 1 article reviews
flow cytometers - by Bioz Stars, 2026-07
99/100 stars
  Buy from Supplier

Image Search Results


Angiogenic potential of muse cells. (A) Representative images showing vascular endothelial markers CD31 expression of mCherry-expressing Muse cells in the ischemic adductor muscles at 7 days after hindlimb ischemia (HLI) surgery. Tissue sections were stained with anti-CD31 antibody (green) and 4′6-diamidino-2-phenylindole (DAPI) (blue). Scale bar, 50 μm. (B) Flow cytometric analysis of CD31 expression in the ischemic adductor muscles at 7 days after HLI surgery ( n = 5). Results are expressed as mean ± SEM of the percentage of mCherry/CD31 double-positive cells per total CD31-positive cell count in the dissociated ischemic adductor muscle. Dots correspond to each mouse. (C) Vascular endothelial growth factor (VEGF) concentration measured by enzyme-linked immunosorbent assay (ELISA) in the cell culture supernatant of Muse cells or non-Muse mesenchymal stem cells (MSCs) under normoxic and hypoxic conditions. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each biological replicate. (D,E) VEGF concentration measured by ELISA in the adductor muscles (D) and relative mRNA expression of representative angiogenic factors in the ischemic adductor muscle (E) at 7 days after HLI surgery. Muse cells or non-Muse MSCs were intravenously injected 1 day after HLI surgery and phosphate buffered saline was injected as a control. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each mouse. * P < 0.05; ** P < 0.01.

Journal: Frontiers in Cardiovascular Medicine

Article Title: Intravenous administration of human Muse cells recovers blood flow in a mouse model of hindlimb ischemia

doi: 10.3389/fcvm.2022.981088

Figure Lengend Snippet: Angiogenic potential of muse cells. (A) Representative images showing vascular endothelial markers CD31 expression of mCherry-expressing Muse cells in the ischemic adductor muscles at 7 days after hindlimb ischemia (HLI) surgery. Tissue sections were stained with anti-CD31 antibody (green) and 4′6-diamidino-2-phenylindole (DAPI) (blue). Scale bar, 50 μm. (B) Flow cytometric analysis of CD31 expression in the ischemic adductor muscles at 7 days after HLI surgery ( n = 5). Results are expressed as mean ± SEM of the percentage of mCherry/CD31 double-positive cells per total CD31-positive cell count in the dissociated ischemic adductor muscle. Dots correspond to each mouse. (C) Vascular endothelial growth factor (VEGF) concentration measured by enzyme-linked immunosorbent assay (ELISA) in the cell culture supernatant of Muse cells or non-Muse mesenchymal stem cells (MSCs) under normoxic and hypoxic conditions. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each biological replicate. (D,E) VEGF concentration measured by ELISA in the adductor muscles (D) and relative mRNA expression of representative angiogenic factors in the ischemic adductor muscle (E) at 7 days after HLI surgery. Muse cells or non-Muse MSCs were intravenously injected 1 day after HLI surgery and phosphate buffered saline was injected as a control. Results are expressed as mean ± SEM ( n = 5). Dots correspond to each mouse. * P < 0.05; ** P < 0.01.

Article Snippet: After erythrocytes were lysed using BD Pharm Lyse (BD Biosciences, 555899), the cells were subjected to flow cytometric analysis (SONY, MA900).

Techniques: Expressing, Muscles, Staining, Cell Counting, Concentration Assay, Enzyme-linked Immunosorbent Assay, Cell Culture, Injection, Saline, Control