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. 2013 May 1;305(1):C111–C120. doi: 10.1152/ajpcell.00026.2013

Table 1.

Colocalization of filamin, CFTR, and RACK1 in Calu-3 cells

Protein1 Protein2 Rpearson Roverlap M1 M2 ICQ n (cells)
Filamin CFTR 0.61 ± 0.04 0.71 ± 0.06 0.28 ± 0.06 0.57 ± 0.07 0.35 ± 0.05 12 (130)
Filamin RACK1 0.70 ± 0.06 0.79 ± 0.04 0.39 ± 0.06 0.57 ± 0.04 0.37 ± 0.02 6 (47)
CFTR RACK1 0.50 ± 0.03 0.60 ± 0.03 0.24 ± 0.04 0.35 ± 0.04 0.29 ± 0.04 8 (80)

All values shown are means ± SE. CFTR, cystic fibrosis transmembrane regulator; RACK1, receptor for activated C kinase 1; Rpearson, Pearson's correlation coefficient (−1; negative correlation, e.g., exclusion; 0: no correlation; 1: positive correlation); Roverlap, overlap correlation coefficient, similar to Pearson's coefficient but without subtraction of the mean intensity values in each channel (0: negative correlation; 1: positive correlation); M1 and M2: Manders coefficients, quantifying the fractional intensity overlap of the first protein's immunofluorescence signal with that of the second protein (M1) and vice versa (M2); ICQ, intensity correlation quotient, as defined by Li et al. (Ref. 6; −0.5: exclusion; 0: random with uncorrelated intensities; 0.5: colocalization with completely correlated intensities between the 2 channels); n (cells): n, total number of imaged fields; cells, total number of cells in these fields