Fig. 3.
Fig. 3. Flow cytometric analysis of human acute leukemia samples by using the MoAbs HSL11, HSL96, and HSL2. Frozen samples of childhood acute leukemia were thawed and stained in the cytoplasm (in a few cases on the cell surface as well) by the MoAbs specific to λ5, VpreB, pre-BCR, μH chain, κL chain, λL chain, CD19, CD22, or CD79b in the same way as in Fig 2. Staining profiles with these MoAbs (thick solid line) and staining profiles with an isotype-matched control MoAb (thin dotted line) are overlaid in the histograms. Though data are not shown, the T-ALL sample was positive for CD3, CD4, and CD8 whereas the AML sample was positive for CD13 and CD33. All data including other leukemia samples are summarized in Tables 2 and 3. Sources of leukemia samples: BM, bone marrow; PB, peripheral blood; LN, lymph node; PE, pleural effusion.

Flow cytometric analysis of human acute leukemia samples by using the MoAbs HSL11, HSL96, and HSL2. Frozen samples of childhood acute leukemia were thawed and stained in the cytoplasm (in a few cases on the cell surface as well) by the MoAbs specific to λ5, VpreB, pre-BCR, μH chain, κL chain, λL chain, CD19, CD22, or CD79b in the same way as in Fig 2. Staining profiles with these MoAbs (thick solid line) and staining profiles with an isotype-matched control MoAb (thin dotted line) are overlaid in the histograms. Though data are not shown, the T-ALL sample was positive for CD3, CD4, and CD8 whereas the AML sample was positive for CD13 and CD33. All data including other leukemia samples are summarized in Tables 2 and 3. Sources of leukemia samples: BM, bone marrow; PB, peripheral blood; LN, lymph node; PE, pleural effusion.

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