An intercalating fluorochrome, PicoGreen, was assessed for its ability to d
etermine the concentration of DNA in clarified mammalian cell culture broth
s containing monoclonal antibodies. Fluorescent signal suppression was amel
iorated by sample dilution or by performing the assay above the pI of secre
ted IgG. The source of fluorescence in clarified culture broth was validate
d by incubation with RNase A and DNase I. At least 91.8% of fluorescence wa
s attributable to nucleic acid and pre-digestion with RNase A was shown to
be a requirement for successful quantification of DNA in such samples.