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- W2053135062 abstract "Binding of the N-terminus of fibronectin to assembly sites on the cell surface is an essential step in fibronectin fibrillogenesis. Fibronectin matrix assembly sites have customarily been quantified using an iodinated 70 kDa N-terminal fibronectin fragment. The 125I-70 K fragment is a less than ideal reagent because its preparation requires large amounts of plasma fibronectin and it has a fairly short shelf life. An additional limitation is that the cells responsible for binding the 125I-70 K cannot be quantified or identified directly but must be assessed in parallel cultures. To overcome these disadvantages, we developed an ELISA-based assay using a recombinant HA-tagged 70 K fragment. This assay allows for the simultaneous quantification and localization of matrix assembly sites on the surface of adherent cells." @default.
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- W2053135062 date "2007-05-01" @default.
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- W2053135062 title "Quantification of fibronectin matrix assembly sites using a novel ELISA assay" @default.
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- W2053135062 doi "https://doi.org/10.1016/j.matbio.2006.12.004" @default.
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