Figure 2
Figure 2. SYK is activated in primary DLBCL tissues. (A) Immunoblotting of total and phosphorylated SYK (pY525/526) in LY7 and LY18 cell lines. Cells were stimulated with (+) or without (-) anti-BCR as described in “Methods.” (B) Immunohistochemical staining of p-SYK (pY525/526) on sections of paraffin cell blocks made from anti-BCR stimulated (+) or unstimulated (-) LY7 and LY18 cells. Photomicrographs were generated using Nikon E600, Planachromat 4/0.10/30.0, 20/0.40/1.3, PlanApo 40/0.095/0.12-0.16, and PlanFluor 40/0.75/0.72 objectives, and were captured using an Olympus DP12 camera. (C-D) Immunohistochemical staining of p-SYK on paraffin-embedded sections from tissue microarray in normal lymphoid tissues (C) and DLBCL tissues (D). The ranges for the scoring system are shown.

SYK is activated in primary DLBCL tissues. (A) Immunoblotting of total and phosphorylated SYK (pY525/526) in LY7 and LY18 cell lines. Cells were stimulated with (+) or without (-) anti-BCR as described in “Methods.” (B) Immunohistochemical staining of p-SYK (pY525/526) on sections of paraffin cell blocks made from anti-BCR stimulated (+) or unstimulated (-) LY7 and LY18 cells. Photomicrographs were generated using Nikon E600, Planachromat 4/0.10/30.0, 20/0.40/1.3, PlanApo 40/0.095/0.12-0.16, and PlanFluor 40/0.75/0.72 objectives, and were captured using an Olympus DP12 camera. (C-D) Immunohistochemical staining of p-SYK on paraffin-embedded sections from tissue microarray in normal lymphoid tissues (C) and DLBCL tissues (D). The ranges for the scoring system are shown.

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