Fig. 1.
Fig. 1. Tyrosine phosphorylation of Shc proteins in normal CD34+ progenitor cells and leukemic CD34+cells. Total cell lysates (20 μg protein) were subjected to Western blot analysis. Phosphotyrosine was identified by antiphosphotyrosine antibody (4G10). Representative blots are shown. The positions of p66Shc, p52Shc, and p46Shc are indicated on the right. Molecular-weight marker bands are indicated on the left. Lanes 1 and 4, enhanced chemiluminescence protein molecular-weight markers; lane 2, Nonstimulated A431 cell lysate; lane 3, epidermal growth factor–stimulated A431 cell lysate; lane 5, CD34+ cells from normal BM; lane 6, CD34− cells from normal BM; lane 7, CD34+cells from AML patient BM; lane 8, CD34− cells from AML patient BM.

Tyrosine phosphorylation of Shc proteins in normal CD34+ progenitor cells and leukemic CD34+cells. Total cell lysates (20 μg protein) were subjected to Western blot analysis. Phosphotyrosine was identified by antiphosphotyrosine antibody (4G10). Representative blots are shown. The positions of p66Shc, p52Shc, and p46Shc are indicated on the right. Molecular-weight marker bands are indicated on the left. Lanes 1 and 4, enhanced chemiluminescence protein molecular-weight markers; lane 2, Nonstimulated A431 cell lysate; lane 3, epidermal growth factor–stimulated A431 cell lysate; lane 5, CD34+ cells from normal BM; lane 6, CD34 cells from normal BM; lane 7, CD34+cells from AML patient BM; lane 8, CD34 cells from AML patient BM.

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