Fig. 1.
Fig. 1. Flow cytometric histograms of Pgp expression in representative AML cases. / Leukemia blasts enriched over density gradients were assessed for Pgp expression using the fluorescence-conjugated Pgp-specific monoclonal antibody MRK16. MRK16 fluorescence, and that of appropriately matched isotype controls, were detected using highly sensitive flow cytometric assays. MRK16 expression was quantitated with the Kolmogorov-Smirnov statistic D. Representative histograms for AML cases in the present study are shown for (A) case considered “Pgp+ high” (defined as D > 0.3) with a D value of 0.45 relative to the isotype control; (B) case considered “Pgp−”(defined as D < 0.2) with a D value of 0.10; (C) “PgP+ low” AML (defined as 0.2 < D < 0.3) with a D value of 0.25 relative to the isotype control; and (D) the Pgp+ DOX 6 cell line used as a positive control for MRK16 staining, with a D value of 0.42 relative to the isotype control.

Flow cytometric histograms of Pgp expression in representative AML cases.

Leukemia blasts enriched over density gradients were assessed for Pgp expression using the fluorescence-conjugated Pgp-specific monoclonal antibody MRK16. MRK16 fluorescence, and that of appropriately matched isotype controls, were detected using highly sensitive flow cytometric assays. MRK16 expression was quantitated with the Kolmogorov-Smirnov statistic D. Representative histograms for AML cases in the present study are shown for (A) case considered “Pgp+ high” (defined as D > 0.3) with a D value of 0.45 relative to the isotype control; (B) case considered “Pgp”(defined as D < 0.2) with a D value of 0.10; (C) “PgP+ low” AML (defined as 0.2 < D < 0.3) with a D value of 0.25 relative to the isotype control; and (D) the Pgp+ DOX 6 cell line used as a positive control for MRK16 staining, with a D value of 0.42 relative to the isotype control.

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