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Single site mutations at asparagine residues were shown to result in a functionally active yet slightly less thermally stable version of the enzyme in vitro, while knockout of all asparagine residues resulted in an accumulation of the uncleaved, propeptide form of the enzyme

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( G ) mCherry high and mCherry low populations were sorted and injected via tail vein into SCID mice (n = 10 cells, n = 10 2 cells, n = 10 3 cells) to generate experimental metastases to the lung