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dc.contributor.advisorArtika, I Made
dc.contributor.advisorKoerniati, Sri
dc.contributor.authorHapsari, Elmita
dc.date.accessioned2015-01-06T02:17:06Z
dc.date.available2015-01-06T02:17:06Z
dc.date.issued2014
dc.identifier.urihttp://repository.ipb.ac.id/handle/123456789/72942
dc.description.abstractArtemisia annua WRKY1 (AaWRKY1) gene encodes a protein WRKY a transcriptional activator of Amorpha-4,11-diene synthase (ADS). The overexpression farnesil diphosphate AaWRKY1 genes can increase levels of artemisinin. This study was aimed to isolate an AaWRKY1 gene from Artemisia annua L. Amplification of AaWRKY1 gene was done by PCR (Polymerase Chain Reaction) technique using specific primer pairs and cDNA as a template. Subsequently, AaWRKY1 gene fragment was cloned into a cloning vector pJET 1.2 using T4-ligase and transformed into competent cell Escherichia coli DH5α through heat shock method, and grown on LB agar medium containing ampicillin. Result showed that amplification with specific primers of AaWRKY1 gene generated an amplicon fragment of ± 1500 bp. The gene fragment was succesfully cloned into pJET 1.2 and transformed into cells of E. coli DH5α. Confirmation of recombinant clone was carried out using colony PCR to obtain recombinant colonies.en
dc.language.isoid
dc.subject.ddcAaWRixYi geneen
dc.subject.ddcBiochemistryen
dc.titleIsolasi dan Kloning pada Escherichia coli Gen AaWRKY1 Artemisia annua Len
dc.subject.keywordBogor Agricultural University (IPB)en
dc.subject.keywordpJET 1.2 Vectoren
dc.subject.keywordcolony PCRen
dc.subject.keywordcloningen
dc.subject.keywordAaWRKY1 geneen
dc.subject.keywordArtemisia annua Len


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