Fig. 7.
Fig. 7. GPI anchoring of DOK1. / (A) K562 cells were transfected with pDI2E construct, and stable transfectants were selected in G418-containing media. The cells were then incubated in PI-PLC (+) or buffer (−) prior to analysis. Flow cytometry was performed using FITC-conjugated anti-CD71, anti-CD59, and Dombrock antisera for comparison. (B) K562 cells and the GPI− cell line transfected either with pI2E or pDI2E DNA and selected in G418-containing media were stained with Dombrock antisera and analyzed by flow cytometry. The mean fluorescence of each population is shown at the top of each panel.

GPI anchoring of DOK1.

(A) K562 cells were transfected with pDI2E construct, and stable transfectants were selected in G418-containing media. The cells were then incubated in PI-PLC (+) or buffer (−) prior to analysis. Flow cytometry was performed using FITC-conjugated anti-CD71, anti-CD59, and Dombrock antisera for comparison. (B) K562 cells and the GPI− cell line transfected either with pI2E or pDI2E DNA and selected in G418-containing media were stained with Dombrock antisera and analyzed by flow cytometry. The mean fluorescence of each population is shown at the top of each panel.

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