1. Shodhganga@INFLIBNET
  2. Indian Institute of Technology Guwahati
  3. DEPARTMENT OF BIOSCIENCES AND BIOENGINEERING
Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/419790
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dc.coverage.spatialBiosciences and Bioengineering
dc.date.accessioned2022-11-16T12:03:33Z-
dc.date.available2022-11-16T12:03:33Z-
dc.identifier.urihttp://hdl.handle.net/10603/419790-
dc.description.abstractRecombinant huIFN 206 177 2b has been expressed on various platforms which includes bacteria yeast insect cell lines mammalian cell lines and plants Expression of recombinant huIFN 206 177 2b in E coli yielded high huIFN 206 177 2b titer but the expressed protein forms inclusion bodies and loses the activity during renaturation process Also the expressed protein lacks post translational modifications and exhibited very less plasma life The plasma life of huIFN 206 177 2b expressed by E coli increased to certain e...
dc.format.extentNot Available
dc.languageEnglish
dc.relationNot Available
dc.rightsself
dc.titleCloning expression process analytical technology pat enabled monitoring and control of glycoengineered pichia pastoris cultivation for human interferon 945 2b production
dc.title.alternativeNot available
dc.creator.researcherSrikanth, Katla
dc.subject.keywordBiochemistry and Molecular Biology
dc.subject.keywordBiology and Biochemistry
dc.subject.keywordLife Sciences
dc.description.noteNot Available
dc.contributor.guideSivaprakasam, Senthilkumar
dc.publisher.placeGuwahati
dc.publisher.universityIndian Institute of Technology Guwahati
dc.publisher.institutionDEPARTMENT OF BIOSCIENCES AND BIOENGINEERING
dc.date.registered2012
dc.date.completed2019
dc.date.awarded2019
dc.format.dimensionsNot Available
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:DEPARTMENT OF BIOSCIENCES AND BIOENGINEERING

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