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3 | 488 | 780/60 | 490 | 764 | (in buffer) 4 | flow cytometry |
NovaFluor dyes, including NovaFluor Red 760 dye, are built using Phiton technology and are compatible with both spectral flow cytometry and traditional flow cytometry. NovaFluor dyes exhibit narrow emission spectra and minimal cross-laser excitation, which helps reduce spectral spillover for better marker resolution. In addition, their unique spectral signatures can provide the opportunity to detect additional markers in flow cytometry panels by opening up previously unusable channels.
NovaFluor Blue 760 dye has a unique emission spectrum when excited by the 488 nm laser, which fits in a spectral space that is currently not accessible by other spectral dyes. Adding spectrally unique dyes may allow for building out larger panels with minimal loss of resolution. NovaFluor Blue 760 dye should generally be paired with moderately to highly expressed antigens in multicolor panels. The macromolecule-based NovaFluor Blue 760 dye produces highly stable fluorescence, and stained samples retain their fluorescence intensity and spectral signature when stored at 4°C.
Benefits of NovaFluor Blue 760 dye
Use NovaFluor dyes with CellBlox Plus Blocking Buffer to reduce background and to block non-specific binding of NovaFluor labels, PE and APC tandems observed with macrophages and monocytes.
Figure 1. Spectral signature of NovaFluor Blue 760 dye. Normal human peripheral blood cells stained with anti-CD4 antibodies (clone SK3) conjugated to NovaFluor Blue 760 dye were used for analysis. Data was acquired on a 5-laser Cytek Aurora system.
Figure 2. NovaFluor Blue 760 conjugated antibody staining performance with mouse splenocytes. C57BL/6 mouse splenocytes were stained with CD45R Monoclonal Antibody, eFluor 450 only (left) or along with CD5 Monoclonal Antibody, NovaFluor Blue 760 (right). Viable cells were used for analysis, as determined by LIVE/DEAD Fixable Blue Dead Cell Stain Kit (Cat. No. L34962).
Figure 3. NovaFluor Blue 760 conjugated antibody staining performance with human PBMCs. Normal human peripheral blood cells were stained with CD14 Monoclonal Antibody, APC-eFluor 450 only (left) or with CD11b Monoclonal Antibody, NovaFluor Blue 760 (right). Cells in the monocyte gate were used for analysis.
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