Fig. 2.
Fig. 2. Role of the cytoplasmic portion of CD34 in tyrosine phosphorylation. (A) Amino acid sequence of the cytoplasmic portions of the full-length CD34 (CD34full; top) and the truncated CD34 (CD34trunc; bottom). Vertical bars indicate conserved residues. PTK, a candidate tyrosine phosphorylation site; PKC, a consensus phosphorylation site for protein kinase C. (B) FACS analysis of U937 cells stably transfected with vector alone, CD34full, or CD34trunc. Cells were stained with anti-CD34 (4A1, solid lines) or with the secondary reagent alone (dotted lines). (C) Western blot of Triton X-100 lysates from U937 cells stably transfected with Vector alone (lane 1), CD34full (lane 2), or CD34trunc (lane 3), probed with anti-CD34 (4A1). (D) Western blots of equal amounts of Triton X-100 lysates from U937 cells stably transfected with vector, CD34full, or CD34trunc, probed with anti-pTyr (4G10). Cells were stimulated for 30 minutes with anti-CD34 (4A1) or MOPC21 (control) as described in the legend to Fig 1. Molecular size markers are indicated on the left (kD).

Role of the cytoplasmic portion of CD34 in tyrosine phosphorylation. (A) Amino acid sequence of the cytoplasmic portions of the full-length CD34 (CD34full; top) and the truncated CD34 (CD34trunc; bottom). Vertical bars indicate conserved residues. PTK, a candidate tyrosine phosphorylation site; PKC, a consensus phosphorylation site for protein kinase C. (B) FACS analysis of U937 cells stably transfected with vector alone, CD34full, or CD34trunc. Cells were stained with anti-CD34 (4A1, solid lines) or with the secondary reagent alone (dotted lines). (C) Western blot of Triton X-100 lysates from U937 cells stably transfected with Vector alone (lane 1), CD34full (lane 2), or CD34trunc (lane 3), probed with anti-CD34 (4A1). (D) Western blots of equal amounts of Triton X-100 lysates from U937 cells stably transfected with vector, CD34full, or CD34trunc, probed with anti-pTyr (4G10). Cells were stimulated for 30 minutes with anti-CD34 (4A1) or MOPC21 (control) as described in the legend to Fig 1. Molecular size markers are indicated on the left (kD).

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