Please use this identifier to cite or link to this item: http://umt-ir.umt.edu.my:8080/handle/123456789/9126
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dc.contributor.authorChin, Sau Mei-
dc.date.accessioned2018-05-23T03:08:46Z-
dc.date.available2018-05-23T03:08:46Z-
dc.date.issued2008-
dc.identifier.urihttp://umt-ir.umt.edu.my:8080/xmlui/handle/123456789/9126-
dc.description.abstractDelta-9-stearoyl-ACP desaturase (SACPD) gene is the key gene in converting the saturated stearoyl-ACP (C:18) to monounsaturated oleoyl-ACP (C 18:1) in fatty acid biosynthesis pathways. Manipulation of delta-9 stearoyl-ACP desaturase gene 1s an important step to enhance the accumulation of oleic acid level, so that, more monounsaturated oleic acid can be produced in Chiarella sp. The RT-PCR technique was used to isolate the SACPD cDNA clone from Chiarella sp. The total RNA was reverse transcribed with KPN-Tl 7 oligo-dT primer by using M-ML V reverse transcriptase. Four forward primers designed from the conserved regions of SACPD gene were used to amplify corresponding 3 '-end regions of the gene.en_US
dc.language.isoenen_US
dc.publisherUniversiti Malaysia Terengganu (UMT)en_US
dc.subjectLP 8 FST 1 2008en_US
dc.subjectChin, Sau Meien_US
dc.titleIsolation of delta-9 stearoyl-acp desaturase gene from Chlorella spen_US
dc.typeOtheren_US
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