参考图片
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 thymocytes (left panel) and splenocytes (right panel). BALB/c mouse thymocytes were stained with APC-conjugated anti-mouse CD4 (clone RM4-5, Cat. No. 553051) and biotinylated anti-mouse CD8a (clone 53-6.7, Cat. No. 553028/553029) (left panel). BALB/c mouse splenocytes were stained with APC-conjugated anti-mouse CD3e (clone 145-2C11, Cat. No. 553066) and biotinylated anti-mouse CD45R/B220 (clone RA3-6B2, Cat. No. 553085/553086) (right panel). The biotin conjugates were revealed with SAv-APC-Cy7. Experiements 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.
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