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Metal-enhanced fluorescence protein assays

The theory and application of this fluorescence method have been discussed in detail by LePecq and others (3,8). The assay requires that there is sufficient ionic strength to minimize ionic binding (e.g., O.IM sodium chloride), that the pH is 4-10, that no heavy metals are present, that the fluorescence is not enhanced on binding to other excipients (e.g., proteins) and that at least portions of the nucleic acids are not complexed. These requirements can usually he met when dealing with recombinant products in some cases the samples must he manipulated to create the appropriate conditions. In the intercalative method of dye binding, proteins rarely interfere with the assay, and procedures have been developed to remove the few interferences they may cause (e.g., the use of heparin or enzymatic digestion of the protein 9). [Pg.46]


See other pages where Metal-enhanced fluorescence protein assays is mentioned: [Pg.552]    [Pg.467]    [Pg.444]    [Pg.444]    [Pg.1239]    [Pg.748]    [Pg.479]    [Pg.283]    [Pg.331]    [Pg.169]    [Pg.282]   
See also in sourсe #XX -- [ Pg.168 , Pg.169 ]




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