Manipulation of UDP-Glc:Glycoprotein Glucosyltransferase (UGGT) Using CRISPR/Cas9 Genome Engineering System

dc.contributor.authorDuffey, Alec
dc.date.accessioned2015-05-12T15:47:58Z
dc.date.available2015-05-12T15:47:58Z
dc.date.issued2015
dc.description1 Broadside. Designed using Microsoft PowerPoint. 48"W x 36"Hen_US
dc.description.abstractGenome engineering is the process of making targeted modifications in the genome. This has become the basis in which DNA alteration can be explored and manipulated. A new form of genome engineering known as clustered regularly interspaced short palindromic repeats (CRISPR) has recently emerged and grants the user the ability for specific target cuts in the genome like never before. This technique was used in this study to investigate and knockout a protein sensor known as UDP-glucose:glycoprotein glucosyltransferase (UGGT) .en_US
dc.description.sponsorshipKalamazoo College. Department of Biology. Diebold Symposium, 2015en_US
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/10920/29638
dc.language.isoen_USen_US
dc.publisherKalamazoo, Mich. : Kalamazoo Collegeen_US
dc.relation.ispartofKalamazoo College Diebold Symposium Presentation Collectionen
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.en
dc.titleManipulation of UDP-Glc:Glycoprotein Glucosyltransferase (UGGT) Using CRISPR/Cas9 Genome Engineering Systemen_US
dc.typePresentationen_US
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