BD Pharmingen- PE Mouse Anti-Human TNFR Related Protein -LT-R_BD Pharmingen
参考图片
Flow cytometric analysis of LTβR expression by HeLa, Jurkat and human monocytes. HeLa cell line (Left Panel), Jurkat cell line (Middle Panel), or human peripheral monocytes (Right Panel) were stained with PE Mouse Anti-Human TNFR Related Protein (LTβR) (Cat No. 551503; filled histograms) or PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; empty histograms) at 0.5 µg/10^6 cells. Whole human blood was first treated with PharmLyse™ Lysing Buffer (Cat No. 555899) to lyse erythrocytes and blocked with normal polyclonal human IgG (5 µg/10^6 cells) prior to staining. Note that certain human cell lines or cell types (e.g., neutrophils, monocytes) can first be treated with reagents that block receptors for the Fc regions of immunoglobulin to avoid nonspecific immunofluorescent staining mediated by Fc receptors. Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable cells.
Flow cytometric analysis of LTβR expression by HeLa, Jurkat and human monocytes. HeLa cell line (Left Panel), Jurkat cell line (Middle Panel), or human peripheral monocytes (Right Panel) were stained with PE Mouse Anti-Human TNFR Related Protein (LTβR) (Cat No. 551503; filled histograms) or PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; empty histograms) at 0.5 µg/10^6 cells. Whole human blood was first treated with PharmLyse™ Lysing Buffer (Cat No. 555899) to lyse erythrocytes and blocked with normal polyclonal human IgG (5 µg/10^6 cells) prior to staining. Note that certain human cell lines or cell types (e.g., neutrophils, monocytes) can first be treated with reagents that block receptors for the Fc regions of immunoglobulin to avoid nonspecific immunofluorescent staining mediated by Fc receptors. Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable cells.
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