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. 2013 Apr 17;15(8):1027–1040. doi: 10.1093/neuonc/not046

Fig. 1.

Fig. 1.

Expression profile and through-passage stability of U251 sublines armed with extra chromosome 7 (c5, c9, c55) or transfected with erbB1 gene (E1L, E1H/L, E1H/H). U251 subclones were labeled for ErbB1 with AlexaFluor 546-528 and for integrin-β1 with AlexaFluor 647-TS2 antibodies, as described in the Material and Methods. (A and B) Number of ErbB1 (Inline graphic) and integrin-β1 (Inline graphic) molecules on the cell surface of U251 subclones transferred with extra chromosome 7 material (A) or transfected with erbB1 gene (B) were quantitated by flow cytometry using QIFIKIT. (C) Number of ErbB1 on U251_E1H/H (Inline graphic), E1H/L (Inline graphic), and E1L (Inline graphic) and number of integrin-β1 on U251_E1H/H (Inline graphic) and E1L (Inline graphic) subclones over 28 passages. (D) Percentage of high (E1H/H) and low (E1H/L) ErbB1 expressing subpopulations of U251_E1H transfectant subline gradually splitting into 2 over the passages.