Browsing by Author "Nurhayati, Siti"
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Item OPTIMASI SUHU ANNEALING UNTUK AMPLIFIKASI DAERAH trnQ-5’ rps16 INTERGENIC SPACER PADA TUMBUHAN PANDAN (Benstonea sp.) ASAL RIAU(2020-08) Nurhayati, Siti; Roslim, Dewi IndriyaniPandan (Benstonea sp.) is one of the most important plant in Kajuik Lake located in Langgam, Riau Province, Indonesia. Polymerase Chain Reaction (PCR) is a technique used to multiply or amplify DNA samples in vitro using a primer pair. trnQ-5’ rps16 intergenic spacer is a pair of primers used to amplify the trnQ- 5’ rps16 intergenic spacer region. This study aimed to optimize annealing temperature of trnQ-5’ rps16 intergenic spacer primer. This research invloved total DNA isolation using Genomic DNA Mini Kit Plant (Geneaid), PCR, and electrophoresis. The result showed that the optimal annealing temperature for amplification of trnQ-5’ rps16 intergenic spacer was 58°C. The PCR product on this annealing temperature was thick DNA with a size of about 950 bp .Item OPTIMASI SUHU ANNEALING UNTUK AMPLIFIKASI DAERAH trnQ-5’rps16 INTERGENIC SPACER PADA TUMBUHAN PANDAN (Benstonea sp.) ASAL RIAU(2020-06) Nurhayati, Siti; Roslim, Dewi IndriyaniPandan (Benstonea sp.) is one of the most important plant in Kajuik Lake located in Langgam, Riau Province, Indonesia. Polymerase Chain Reaction (PCR) is a technique used to multiply or amplify DNA samples in vitro using a primer pair. This study aims to optimize annealing temperature of trnQ-5’rps16 intergenic spacer primer. Stages of research are total DNA isolation using Genomic DNA Mini Kit Plant (Geneaid), PCR and electrophoresis. The result showed that the optimal annealing temperature for amplification of trnQ-5’rps16 intergenic spacer is 58°C. The PCR product on this annealing temperature is thick.