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. 2012 Nov 11;2012:989372. doi: 10.1155/2012/989372

Figure 3.

Figure 3

Establishing iPLA 2 γ-knockdown INS-1 cell lines. INS-1 cells were transfected with FIV constructs containing inserts that produced either scrambled RNA (control) or siRNA directed against sequences in iPLA2 γ mRNA (KD1, KD2). The relative iPLA2 γ expression levels in control INS-1 cells and in the iPLA2 γ-knockdown (KD) cell lines KD1 and KD2 were assessed by quantitative PCR for mRNA (panel (a)) and by Western blotting analysis for iPLA2 γ-immunoreactive protein (panel (b)). In panel (a), mean values ± SEM are displayed (n = 4). An asterisk (*) denotes a significant difference (P < 0.05) from the value for control INS-1 cells. The immunoblot in panel (b) is representative of four experiments.