Fetal bovine serum impacts the observed N‐glycosylation defects in TMEM165 KO HEK cells
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DOI: 10.1002/jimd.12161
Abstract: TMEM165 is involved in a rare genetic human disease named TMEM165‐CDG (congenital disorders of glycosylation). It is Golgi localized, highly conserved through evolution and belongs to the uncharacterized protein family 0016 (UPF0016). The use of… read more here.
Keywords: fetal bovine; glycosylation defects; glycosylation; hek cells ... See more keywords