Detection of Glycosylated and Deglycosylated Extensin Precursors by Indirect Competitive ELISA
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A competitive indirect enzyme-linked immunosorbent assay (ELISA) was developed for the rapid quantitation of the glycosylated and deglycosylated forms of the monomeric soluble extensin precursor subunits P1 and P2. A log-linear response range for each kind of precursor in the competition curve was between 0.01 and 100 nanograms per milliliter.
Antibody localization of extensin in cell walls of carrot storage roots.
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