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  4. Dissertation, BC
Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/8433
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dc.contributor.authorPatel, Yesha-
dc.contributor.authorMemon, Shifa-
dc.date.accessioned2019-07-05T09:27:08Z-
dc.date.available2019-07-05T09:27:08Z-
dc.date.issued2019-04-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/8433-
dc.descriptionSDR00336en_US
dc.description.abstractConclusion In this study, we successfully identified the Sar1a GTPase from E. histolytica genome database. The identified putative 573-bp of Sar1a GTPase sequence (EHI_031410A) was efficiently cloned into a pEhex-HA amoebic expression vector. The sequence identity and fidelity of cloned Sar1a GTPase (573-bp) was confirmed by automated Sanger sequencing. The confirmed pEhex-HA-Sar1a construct will be further used in sub-cellular localization and functional studies in E. histolytica trophozoite.en_US
dc.language.isoen_USen_US
dc.publisherInstitute of Science, Nirma Universityen_US
dc.relation.ispartofseries;SDR00336-
dc.subjectBiochemistryen_US
dc.subjectProject Reporten_US
dc.subjectProject Report 2019en_US
dc.subjectBiochemistry Project Reporten_US
dc.subject17MMBen_US
dc.subject17MMB024en_US
dc.subject17MBTen_US
dc.subject17MBT036en_US
dc.titleCloning of Sar1a GTPases Homologue from Entamoeba Histolyticaen_US
dc.typeDissertationen_US
Appears in Collections:Dissertation, BC

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