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. 2010 Apr;129(4):589–599. doi: 10.1111/j.1365-2567.2009.03161.x

Figure 2.

Figure 2

p21Cip1 induced by n-butyrate was maintained in anergic T helper type 1 (Th1) cells. The Th1 cells were stimulated with keyhole limpet haemocyanin (day 0). n-Butyrate was added to some of the Th1 cells on day 1 (D1). Total cell lysates were prepared daily during the 6-day primary culture and Western blot analysis of p21Cip1 (a) and other cell-cycle proteins (b) was performed. Because n-butyrate was added to the cultures at the end of day 1, there is a common day 1 (D1) lane for the two groups. As there was insufficient material, the D1 level of some proteins could not be included. Densitometric analysis of the p21Cip1 levels was performed and the are results presented as per cent adjusted volume (PAV). Day 6 levels of p21Cip1 were studied in four separate experiments with consistent results.