Figure 1
Figure 1. Gal1 expression in EBV-transformed LCLs and primary EBV+ PTLDs. (A) Gal1 expression in a cHL cell line (L428), a series of EBV-transformed LCLs (NOR-, RIC-, STA-, FOL-, LOV-, RIV-, WOL-, FW-, VS-, MA-, SC-, DS-, and DW-LCL), and a DLBCL cell line (SU-DHL6). (B) Gal1 immunohistochemical staining of 3 representative primary EBV+ PTLDs (i-iii) and a DLBCL (iv). In subpanel iv, a Gal1+ macrophage is indicated with a red arrow and representative Gal1− DLBCL tumor cells are indicated with black arrows. The recently developed murine αGal1 mAb 8F4F8G7 was used at 1:20 000 (final concentration, 250 ng/mL) for immunoblots (A) and at 1:40 000 (final concentration, 125 ng/mL) for immunohistochemistry (B). Original magnifications are 1000×.

Gal1 expression in EBV-transformed LCLs and primary EBV+ PTLDs. (A) Gal1 expression in a cHL cell line (L428), a series of EBV-transformed LCLs (NOR-, RIC-, STA-, FOL-, LOV-, RIV-, WOL-, FW-, VS-, MA-, SC-, DS-, and DW-LCL), and a DLBCL cell line (SU-DHL6). (B) Gal1 immunohistochemical staining of 3 representative primary EBV+ PTLDs (i-iii) and a DLBCL (iv). In subpanel iv, a Gal1+ macrophage is indicated with a red arrow and representative Gal1 DLBCL tumor cells are indicated with black arrows. The recently developed murine αGal1 mAb 8F4F8G7 was used at 1:20 000 (final concentration, 250 ng/mL) for immunoblots (A) and at 1:40 000 (final concentration, 125 ng/mL) for immunohistochemistry (B). Original magnifications are 1000×.

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