参考图片
Flow cytometric analysis of mouse CD22.2 and rat CD45RA expression using APC Rat Anti-Mouse IgG1 antibody as a second step. Left Plot: CD22.2 expression on mouse splenocytes. BALB/c mouse splenic leucocytes were either not stained (control staining; dashed line histogram) or stained with Purified Mouse IgG1, κ Anti-Mouse CD22.2 antibody (solid line histogram). After washing, the cells were then stained with APC Rat Anti-Mouse IgG1 antibody (Cat. No. 550874) at 1 µg/test. The fluorescence histogram showing CD22.2 expression (or control staining) was derived from gated events with the forward and side light-scatter characteristics of intact leucocytes. Right Plot: CD45RA expression on rat splenocytes. Rat splenic leucocytes were either not stained (control staining; dashed line histogram) or stained with Purified Mouse IgG1, κ Anti- Rat CD45RA antibody (Cat. No. 554882; solid line histogram). After washing, the cells were then stained with APC Rat Anti-Mouse IgG1 antibody at 1 µg/test. The fluorescence histogram showing CD45RA expression (or control staining) was derived from gated events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry and data analysis was performed using a BD LSRFortessa™ X-20 Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
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