Zobrazeno 1 - 4
of 4
pro vyhledávání: '"protein radiolabelling"'
Publikováno v:
Journal of Labelled Compounds & Radiopharmaceuticals
Morris, O, Mcmahon, A, Boutin, H, Grigg, J & Prenant, C 2016, ' Automation of [18F]fluoroacetaldehyde synthesis: application to a recombinant human interleukin-1 receptor antagonist (rhIL-1RA) ', Journal of Labelled Compounds and Radiopharmaceuticals, vol. 59, no. 7, pp. 277-283 . https://doi.org/10.1002/jlcr.3393
Morris, O, Mcmahon, A, Boutin, H, Grigg, J & Prenant, C 2016, ' Automation of [18F]fluoroacetaldehyde synthesis: application to a recombinant human interleukin-1 receptor antagonist (rhIL-1RA) ', Journal of Labelled Compounds and Radiopharmaceuticals, vol. 59, no. 7, pp. 277-283 . https://doi.org/10.1002/jlcr.3393
[(18) F]Fluoroacetaldehyde is a biocompatible prosthetic group that has been implemented pre-clinically using a semi-automated remotely controlled system. Automation of radiosyntheses permits use of higher levels of [(18) F]fluoride whilst minimising
Autor:
Ana Paula Pêgo, Cátia D. F. Lopes, Ismael Neiva, Isabel F. Amaral, Ana M. Piloto, Charles James Kirkpatrick, Mário A. Barbosa, F. Ferreira da Silva, Susana Sousa
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
The present study aimed to develop a pre-endothelialized chitosan (CH) porous hollowed scaffold for application in spinal cord regenerative therapies. CH conduits with different degrees of acetylation (DA; 4% and 15%) were prepared, characterized (mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fb8794b8591aa83cc281b38afea4e7a
https://hdl.handle.net/10400.22/3343
https://hdl.handle.net/10400.22/3343
Autor:
Badar, Adam, Williams, Jennifer, de Rosales, Rafael TM, Tavaré, Richard, Kampmeier, Florian, Blower, Philip J, Mullen, Gregory ED
Publikováno v:
EJNMMI Research
Background To date, the majority of protein-based radiopharmaceuticals have been radiolabelled using non-site-specific conjugation methods, with little or no control to ensure retained protein function post-labelling. The incorporation of a hexahisti
Akademický článek
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