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. 2001 Mar 13;98(6):3328–3333. doi: 10.1073/pnas.041614798

Figure 2.

Figure 2

Functional activity of the truncated ΔhMCIP1 protein product compared with full-length hMCIP1, assessed by inhibition of calcineurin-dependent activation in C2C12 myoblasts. C2C12 cells were transfected with a luciferase reporter gene driven by a calcineurin-responsive IL-2 promoter (IL-2-Luc). Cells were cotransfected with a constitutively active calcineurin expression plasmid (pCMV-CnA*) and either an empty control vector (pCMV-neo) or the indicated MCIP-encoding plasmid (pCMV-hMCIP1 or pCMV-ΔhMCIP1).