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The assay was designed to demonstrate the biochemical activity of c-met binding sites including Y198 and Y250 (in K1 and K2 domains of HGF, respectively) by significant changes in optical absorbance (expressed as relative unit) within a range from a baseline level (a negative control without HGF
ZnT10, though classically assigned to Golgi and endosomal compartments, can also traffic to the plasma membrane under specific conditions, such as high extracellular zinc or altered manganese levels, possessing a dynamic role in metal detoxification 32
H.LeplaeR.BernardC.VerbruggenN
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