Fig. 2.
Fig. 2. PU.1 expression in Hodgkin cell lines and transient cotransfections of the Hodgkin cell lines L428 and KM-H2 with immunoglobulin enhancer constructs. / (A) Western blot analysis of cell lysate proteins from Hodgkin (lanes 1-6), non-Hodgkin (Burkitt lymphoma: Daudi, Namalwa; pre-B cell line: Reh; lanes 7-9) cell lines and mature CD19+ B cells (B cells; lane 10), showing bands of PU.1 and Spi-B. Left margin, size markers in kilodalton. L428 (B) and KM-H2 (C) cells were transfected with luciferase reporter plasmids driven by conalbumin promoter with or without the MluI-HpaI fragment of the human IgH gene intronic enhancer (pEcona and pcona). Expression vectors for PU.1, Oct2, and BOB/OBF.1 were cotransfected as indicated. Relative luciferase activity is shown and transfections with empty expression vectors were arbitrarily set to 1.

PU.1 expression in Hodgkin cell lines and transient cotransfections of the Hodgkin cell lines L428 and KM-H2 with immunoglobulin enhancer constructs.

(A) Western blot analysis of cell lysate proteins from Hodgkin (lanes 1-6), non-Hodgkin (Burkitt lymphoma: Daudi, Namalwa; pre-B cell line: Reh; lanes 7-9) cell lines and mature CD19+ B cells (B cells; lane 10), showing bands of PU.1 and Spi-B. Left margin, size markers in kilodalton. L428 (B) and KM-H2 (C) cells were transfected with luciferase reporter plasmids driven by conalbumin promoter with or without the MluI-HpaI fragment of the human IgH gene intronic enhancer (pEcona and pcona). Expression vectors for PU.1, Oct2, and BOB/OBF.1 were cotransfected as indicated. Relative luciferase activity is shown and transfections with empty expression vectors were arbitrarily set to 1.

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