Figure 1.
Experimental setup and functional validation of LSC populations. (A) Integration of proteomic (top row) and transcriptomic (bottom row) data sets of healthy HSPC (left column), LSC and non-LSC populations (right column). Proteome of AML samples (top right) was published earlier.12 (B) Leukemic engraftment potential of sorted populations per patient. Mustard shading indicates populations used for proteomics and transcriptomics; light mustard shading, populations used for additional transcriptomics. (C) Flow cytometric analysis of CD34 and CD38 expression of pooled healthy samples used for proteome. Live, lineage-negative cells are shown, and numbers represent gated events of phenotypic HSPCs. NK, normal karyotype.

Experimental setup and functional validation of LSC populations. (A) Integration of proteomic (top row) and transcriptomic (bottom row) data sets of healthy HSPC (left column), LSC and non-LSC populations (right column). Proteome of AML samples (top right) was published earlier.12  (B) Leukemic engraftment potential of sorted populations per patient. Mustard shading indicates populations used for proteomics and transcriptomics; light mustard shading, populations used for additional transcriptomics. (C) Flow cytometric analysis of CD34 and CD38 expression of pooled healthy samples used for proteome. Live, lineage-negative cells are shown, and numbers represent gated events of phenotypic HSPCs. NK, normal karyotype.

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