BD IMag- Anti-Mouse CD90-2 Magnetic Particles - DM_BD Pharmingen
参考图片
Positive selection and depletion of mouse CD90.2-positive splenocytes. Leukocytes were labeled with BD IMag™ anti-mouse CD90.2 Particles - DM (Cat. No. 551518) as described in the protocol. After labeling, the cells were separated using the BD IMag™ Cell Separation Magnet (Cat. No. 552311), and the negative (CD90.2-) and positive (CD90.2+) fractions were collected. Please refer to the Separation Flow Chart to identify the separated cell populations represented in this figure. For flow cytometric analysis, fresh splenocytes (left panel), the negative fraction (middle panel), and the positive fraction (right panel) were stained with FITC Anti-Mouse CD3e (Cat. No. 553061) and PE Anti-mouse CD90.2 (Cat. No. 553005). The percent CD3e+/CD90.2+ cells in each sample is given in the upper right corner.
Positive selection and depletion of mouse CD90.2-positive splenocytes. Leukocytes were labeled with BD IMag™ anti-mouse CD90.2 Particles - DM (Cat. No. 551518) as described in the protocol. After labeling, the cells were separated using the BD IMag™ Cell Separation Magnet (Cat. No. 552311), and the negative (CD90.2-) and positive (CD90.2+) fractions were collected. Please refer to the Separation Flow Chart to identify the separated cell populations represented in this figure. For flow cytometric analysis, fresh splenocytes (left panel), the negative fraction (middle panel), and the positive fraction (right panel) were stained with FITC Anti-Mouse CD3e (Cat. No. 553061) and PE Anti-mouse CD90.2 (Cat. No. 553005). The percent CD3e+/CD90.2+ cells in each sample is given in the upper right corner.
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