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. Author manuscript; available in PMC: 2009 Aug 1.
Published in final edited form as: Mol Genet Metab. 2008 May 15;94(4):491–497. doi: 10.1016/j.ymgme.2008.03.019

Fig. 3. Recombinant human frataxin56–210 and endogenous human frataxin in whole cell extracts exhibit similar binding profiles.

Fig. 3

Samples of recombinant frataxin56–210 and cellular frataxin (from lymphoblast cell extract) were prepared at concentrations empirically determined to generate approximately equal dipstick signals (~25,000 units). The two samples were then serially diluted in 2-fold steps, frataxin levels measured, and the results plotted by pairing the starting high end samples and each pair of subsequent 2-fold diluted samples. The strong linear relationship between the two sample sets indicates immunological equivalence of the two forms of frataxin as measured in the dipstick assay.