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Sample staining on mouse thymocytes (left panel) and splenocytes (right panel). BALB/c mouse thymocytes were stained with APC Rat Anti-Mouse CD4 (Cat. No. 553051) and Biotin Rat Anti-Mouse CD8a (Cat. No. 553028/553029). BALB/c mouse splenocytes were stained with APC Hamster Anti-Mouse CD3e (Cat. No. 553066) and Biotin Rat Anti-Mouse CD45R/B220 (Cat. No. 553085/553086). The biotin conjugates were visualized with Streptavidin APC-Cy™7 (Cat. No.554063). Experiments were performed on a dual-laser FACSVantage™ flow cytometry system equipped with a HeNe laser. APC-Cy7 fluorescence was collected in the FL4 PMT channel, and APC fluorescence was collected in the FL5 PMT channel.
APC-Cy7 spectra. The absorption spectrum of SAv-APC-Cy7 is presented with the corresponding emission spectrum, at the excitation wavelength of 635 nm.
Sample staining on mouse thymocytes (left panel) and splenocytes (right panel). BALB/c mouse thymocytes were stained with APC Rat Anti-Mouse CD4 (Cat. No. 553051) and Biotin Rat Anti-Mouse CD8a (Cat. No. 553028/553029). BALB/c mouse splenocytes were stained with APC Hamster Anti-Mouse CD3e (Cat. No. 553066) and Biotin Rat Anti-Mouse CD45R/B220 (Cat. No. 553085/553086). The biotin conjugates were visualized with Streptavidin APC-Cy™7 (Cat. No.554063). Experiments were performed on a dual-laser FACSVantage™ flow cytometry system equipped with a HeNe laser. APC-Cy7 fluorescence was collected in the FL4 PMT channel, and APC fluorescence was collected in the FL5 PMT channel.
APC-Cy7 spectra. The absorption spectrum of SAv-APC-Cy7 is presented with the corresponding emission spectrum, at the excitation wavelength of 635 nm.
Sample staining on mouse thymocytes (left panel) and splenocytes (right panel). BALB/c mouse thymocytes were stained with APC Rat Anti-Mouse CD4 (Cat. No. 553051) and Biotin Rat Anti-Mouse CD8a (Cat. No. 553028/553029). BALB/c mouse splenocytes were stained with APC Hamster Anti-Mouse CD3e (Cat. No. 553066) and Biotin Rat Anti-Mouse CD45R/B220 (Cat. No. 553085/553086). The biotin conjugates were visualized with Streptavidin APC-Cy™7 (Cat. No.554063). Experiments were performed on a dual-laser FACSVantage™ flow cytometry system equipped with a HeNe laser. APC-Cy7 fluorescence was collected in the FL4 PMT channel, and APC fluorescence was collected in the FL5 PMT channel.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Sav-APC-Cy7 is a useful second-step reagent for the indirect immunofluorescent staining of cells in combination with biotinylated primary antibodies for flow cytometric analysis. SAv-APC-Cy7/biotin conjugates can be used with APC-conjugated reagents to provide two independent staining parameters from a HeNe laser. When choosing reagents for a multicolor staining protocol, we recommend that the APC-Cy7 fluorochrome be reserved for detection of high-density antigens to assure adequate discrimination of antigen expression.
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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.