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purification de l’ARNm

purification de l’ARNm

Behzad Ahmadabadi NILI / Khaled Edbey / Mauro Luisetto

57,03 €
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Editorial:
KS OmniScriptum Publishing
Año de edición:
2022
Materia
Química
ISBN:
9786205347478
57,03 €
IVA incluido
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m R.N.A. La production de VACCINS comme d’autres produits biopharmaceutiques nécessite plusieurs étapes de purification dans le processus de fabrication : T.F.F., filtration à flux tangentiel, suivie de différentes procédures chromatographiques (séparation par affinité et échange d’ions) avec différents types de résines, puis de la technique UF/DF (ultrafiltration-diafiltration). (Il est donc intéressant de vérifier le matériel utilisé pour ce type de procédure en tant que phases solides ou pour la membrane et si des impuretés sont libérées dans le produit final. Pour les garnitures de phase inversée à base de silice, le pourcentage de charge de carbone indique la quantité de phase fonctionnelle liée au matériau de base de la silice. Le but de ce travail est d’étudier le rôle joué par cette caractéristique dans le processus de séparation de l’A.R.N. m.Le but de ce travail est d’étudier le rôle joué par ces caractéristiques dans le processus de séparation du m R.N.A. Parce que ce paramètre influence le temps de rétention, il est intéressant d’évaluer l’utilisation dans la technique de séparation des biopharmaceutiques, et ce également pour les cols de silice recouverts de carbone. Le gel de silice pour la chromatographie peut être produit par un processus systématique, mais également sous forme de Rice traité à haute température. Quel type d’effet peut être joué en utilisant un niveau élevé de matériau de silice recouvert de carbone ?

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