Figure 1
Figure 1. MCPyV detection by FISH in previously reported MCC and CLL cases.1,4 MCPyV FISH was carried out using tyramide signal amplification (TSA) as described previously.3,5 Signal evaluation was performed with a Leica DM 5000 B fluorescence microscope (Leica) using 1000× magnification and specific filter sets for Texas red to visualize MCPyV (A,C,E,G) and DAPI showing blue nuclear counterstaining (B,D,F,H). (A-B) MCPyV detection in MCC and corresponding DAPI (B). (C-D) Negative control on MCC tissue without probe and corresponding DAPI (D). (E-F) MCPyV detection in CLL cells of a bone marrow trephine and corresponding DAPI (F). (G-H) MCPyV detection in another CLL case in a bone marrow trephine and corresponding DAPI (H).

MCPyV detection by FISH in previously reported MCC and CLL cases.1,4  MCPyV FISH was carried out using tyramide signal amplification (TSA) as described previously.3,5  Signal evaluation was performed with a Leica DM 5000 B fluorescence microscope (Leica) using 1000× magnification and specific filter sets for Texas red to visualize MCPyV (A,C,E,G) and DAPI showing blue nuclear counterstaining (B,D,F,H). (A-B) MCPyV detection in MCC and corresponding DAPI (B). (C-D) Negative control on MCC tissue without probe and corresponding DAPI (D). (E-F) MCPyV detection in CLL cells of a bone marrow trephine and corresponding DAPI (F). (G-H) MCPyV detection in another CLL case in a bone marrow trephine and corresponding DAPI (H).

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