cd49f pe conjugated antibody Search Results


facs human mouse  (R&D Systems)
93
R&D Systems facs human mouse
Facs Human Mouse, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/facs human mouse/product/R&D Systems
Average 93 stars, based on 1 article reviews
facs human mouse - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier
cd49f pe  (R&D Systems)
94
R&D Systems cd49f pe
Cells for flow cytometry analysis were cultured for 5 days, and only lineage-negative (CD31-PE, CD45-PE, and CD140b-PE negative) cells were gated for the analysis. ( A ) <t>CD49f/EpCAM</t> staining patterns ( n = 9). ( B ) The number of CD49f + /EpCAM − cells varied on the basis of O 2 tension and tumor type. ( C ) EpCAM positivity also showed tumor-specific variability under physioxia compared to ambient air. ( D ) CD24/CD44 staining patterns of cells from ascites fluid under physioxia and ambient air ( n = 9). ( E ) Percentage of CD44 + cells in each sample under physioxia and ambient air. ( F ) Percentage of CD24 + cells under physioxia and ambient air. CD24 + cells were lower under physioxia compared to ambient air. ( G ) Cells from ascites fluids collected under physioxia contained elevated levels of BRD4 protein compared to cells collected under ambient air.
Cd49f Pe, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd49f pe/product/R&D Systems
Average 94 stars, based on 1 article reviews
cd49f pe - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier

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Cells for flow cytometry analysis were cultured for 5 days, and only lineage-negative (CD31-PE, CD45-PE, and CD140b-PE negative) cells were gated for the analysis. ( A ) CD49f/EpCAM staining patterns ( n = 9). ( B ) The number of CD49f + /EpCAM − cells varied on the basis of O 2 tension and tumor type. ( C ) EpCAM positivity also showed tumor-specific variability under physioxia compared to ambient air. ( D ) CD24/CD44 staining patterns of cells from ascites fluid under physioxia and ambient air ( n = 9). ( E ) Percentage of CD44 + cells in each sample under physioxia and ambient air. ( F ) Percentage of CD24 + cells under physioxia and ambient air. CD24 + cells were lower under physioxia compared to ambient air. ( G ) Cells from ascites fluids collected under physioxia contained elevated levels of BRD4 protein compared to cells collected under ambient air.

Journal: Science Advances

Article Title: Tumor collection/processing under physioxia uncovers highly relevant signaling networks and drug sensitivity

doi: 10.1126/sciadv.abh3375

Figure Lengend Snippet: Cells for flow cytometry analysis were cultured for 5 days, and only lineage-negative (CD31-PE, CD45-PE, and CD140b-PE negative) cells were gated for the analysis. ( A ) CD49f/EpCAM staining patterns ( n = 9). ( B ) The number of CD49f + /EpCAM − cells varied on the basis of O 2 tension and tumor type. ( C ) EpCAM positivity also showed tumor-specific variability under physioxia compared to ambient air. ( D ) CD24/CD44 staining patterns of cells from ascites fluid under physioxia and ambient air ( n = 9). ( E ) Percentage of CD44 + cells in each sample under physioxia and ambient air. ( F ) Percentage of CD24 + cells under physioxia and ambient air. CD24 + cells were lower under physioxia compared to ambient air. ( G ) Cells from ascites fluids collected under physioxia contained elevated levels of BRD4 protein compared to cells collected under ambient air.

Article Snippet: The antibodies used against mouse cells were CD31-PE/Cyanine7 (A14715) from Molecular Probes; CD45-PE/Cyanine7 (25-0451-82), EpCAM-APC (allophycocyanin) (17-5791-82), and CD29-FITC (fluorescein isothiocyanate) (11-0291-82) from Invitrogen; CD140a-PE/Cyanine7 (323508) from BioLegend; LGR5-PE (phycoerythrin) (FAB8240P), TSPAN8-APC (FAB6524A), and CD49f-PE (FAB13501P) from R&D Systems; and CD61-FITC (561911), CD274-PE (558091), CD24-APC (562349), and CXCR4-FITC (551967) from BD Pharmingen; isotype control antibodies used included PE/Cyanine7 (400522) and APC (400612) from BioLegend and PE (554689) and FITC (553971) from BD Pharmingen.

Techniques: Flow Cytometry, Cell Culture, Staining