Приказ основних података о документу

dc.creatorAnđelković, Uroš
dc.creatorGiacometti, Jasminka
dc.creatorJosić, Đuro
dc.date.accessioned2021-02-11T20:17:51Z
dc.date.available2021-02-11T20:17:51Z
dc.date.issued2017
dc.identifier.isbn978-0-12-805392-8
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4233
dc.description.abstractSince the introduction of suitable, highly porous supports and later nonporous and monolithic supports, chromatography has been an indispensibleindispensable method for protein separations on the analytical and preparative scales. The most frequently used methods for protein chromatography are ion exchange, reversed- phase, hydrophobic hydrophobic-interaction chromatography, chromatography on hydroxyapatite and different types of affinity, and pseudo-affinity chromatography. Because of the use of organic solvents during the separation in reversed-phase chromatography, denaturation and loss of biological activity frequently occurs, and this method is less suitable for the separation of biologically active, therapeutic proteins. Chromatography on monolithic supports and chromatography in the displacement mode offer additional opportunities for fast, highly effective separation of proteins on both the analytical and preparative scales.sr
dc.language.isoensr
dc.publisherElseviersr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172048/RS//
dc.rightsrestrictedAccesssr
dc.sourceLiquid Chromatography: Applicationssr
dc.subjectLiquid chromatographysr
dc.subjectProtein fractionationsr
dc.subjectPeptide separationssr
dc.titleProtein and Peptide Separationssr
dc.typebookPartsr
dc.rights.licenseARRsr
dcterms.abstractAнђелковић, Урош; Гиацометти, Јасминка; Јосић, Ђуро; Протеин анд Пептиде Сепаратионс; Протеин анд Пептиде Сепаратионс;
dc.citation.volume2
dc.citation.spage107
dc.citation.epage157
dc.identifier.doi10.1016/B978-0-12-805392-8.00005-0
dc.identifier.scopus2-s2.0-85032478892
dc.type.versionpublishedVersionsr


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Приказ основних података о документу