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A vector for the expression of recombinant monoclonal Fab fragments in bacteria

✍ Scribed by Roberto Burioni; Paola Plaisant; Francesca Bugli; Valeria Delli Carri; Massimo Clementi; Giovanni Fadda

Book ID
114052029
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
138 KB
Volume
217
Category
Article
ISSN
0022-1759

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A system has been developed for synthesis and rapid purification of recombinant polypeptides expressed in frame with glutathione S-transferase (D. B. Smith and K. S. Johnson, 1988, Gene 67, 31-40). Expressed fusion proteins are purified from bacterial extracts by glutathione-agarose affinity chromat