Fig. 6.
Fig. 6. Some of the myristylated Syk constitutively localizes to the GEM fraction along with Lyn, LAT, and FcεRI. / (A) The association of signaling molecules in the GEM fraction in RBL-2H3 cells. Lysates from nonstimulated RBL-2H3 cells were fractionated by sucrose density gradient centrifugation, and 12 μL each fraction was analyzed by immunoblotting with anti-pTyr, Lyn, LAT, FcεRIβ, and γ antibodies. (B) RBL-2H3 cells and cells expressingmyr-Syk (A28) were either nonstimulated or stimulated with antigen (Ag), and cell homogenates were fractionated by sucrose density gradient centrifugation and analyzed by immunoblotting with anti-Syk antibody. Similar results were obtained in 3 independent experiments.

Some of the myristylated Syk constitutively localizes to the GEM fraction along with Lyn, LAT, and FcεRI.

(A) The association of signaling molecules in the GEM fraction in RBL-2H3 cells. Lysates from nonstimulated RBL-2H3 cells were fractionated by sucrose density gradient centrifugation, and 12 μL each fraction was analyzed by immunoblotting with anti-pTyr, Lyn, LAT, FcεRIβ, and γ antibodies. (B) RBL-2H3 cells and cells expressingmyr-Syk (A28) were either nonstimulated or stimulated with antigen (Ag), and cell homogenates were fractionated by sucrose density gradient centrifugation and analyzed by immunoblotting with anti-Syk antibody. Similar results were obtained in 3 independent experiments.

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