PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 24668066-1 2014 Conventional N-glycoproteome analysis usually applies C18 reversed-phase (RP) adsorbent for sample purification, which will lead to unavoidable sample loss due to the high hydrophilicity of N-glycopeptides. n-glycopeptides 190-205 Bardet-Biedl syndrome 9 Homo sapiens 54-57 24668066-3 2014 It was observed that the small hydrophilic N-glycopeptides that cannot retain onto C18 adsorbent can be captured by the graphitized carbon, while the large hydrophobic N-glycopeptides that cannot retain onto the graphitized carbon can be feasibly captured by the C18 adsorbent. n-glycopeptides 43-58 Bardet-Biedl syndrome 9 Homo sapiens 83-86 24668066-4 2014 Comparing with sample purification by using C18 adsorbent only, 28.5 % more N-glycopeptides were identified by combining both C18 and PGC adsorbents. n-glycopeptides 76-91 Bardet-Biedl syndrome 9 Homo sapiens 44-47 24668066-4 2014 Comparing with sample purification by using C18 adsorbent only, 28.5 % more N-glycopeptides were identified by combining both C18 and PGC adsorbents. n-glycopeptides 76-91 Bardet-Biedl syndrome 9 Homo sapiens 126-129