DINI NURKHASANAH, . (2017) ISOLASI, AMPLIFIKASI DAN KARAKTERISASI GEN fim-C BAKTERI Salmonella typhi DAN Shigella dysenteriae. Sarjana thesis, UNIVERSITAS NEGERI JAKARTA.
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Abstract
Penelitian ini bertujuan untuk mengisolasi DNA bakteri Salmonella typhi dan Shigella dysenteriae menggunakan GeneJET Genomic DNA Purification Kit #K0721, #K0722 (Thermo Scientific), amplifikasi gen fim-C bakteri Salmonella typhi dan Shigella dysenteriae dengan metode Polimerase Chain Reaction (PCR) dan karakterisasi gen fim-C dengan menggunakan elektroforesisi gel agarosa 2%. DNA genom bakteri Salmonella typhi dan Shigella dysenteriae telah berhasil diisolasi dan diperoleh konsentrasi DNA masing – masing sebesar 121.0 ng/µL dan 45.5 ng/µL. DNA genom bakteri Salmonella typhi dan Shigella dysenteriae masing – masing dilakukan proses amplifikasi terhadap sepasang primer DNA bakteri Salmonella typhi dan Shigella dysenteriae dari gen fim-C dengan metode PCR dan hasil amplifikasi dikarakterisasi menggunakan elektroforesisi gel agarosa 2%. Pasangan primer bakteri Shigella dysenteriae mampu mengamplifikasi DNA bakteri Shigella dysenteriae pada suhu annealing 56°C dengan munculnya pita (band) pada fragmen ± 95 pb, ± 700 pb dan ± 1000 pb. Pasangan primer bakteri Salmonella typhi mampu mengamplifikasi DNA bakteri Salmonella typhi pada suhu annealing 56°C dengan munculnya pita (band) pada fragmen ± 95 pb. This study purpose to isolated the DNA of Salmonella typhi and Shigella dysentericae using GeneJET Genomic DNA Purification Kit #K0721, #K0722 (Thermo Scientific), amplification the bacteri fim-C gene of Salmonella typhi and Shigella dysenteriae using Polimerase Chain Reaction (PCR) method, and characterize the fim-C gene using 2% agarose gel electrophoresis. The DNA genome of Salmonella typhi and Shigella dysenteriae has isolated with DNA concentration was 121.0 ng/µL dan 45.5 ng/µL. The DNA genomes was amplified to primer pairs fim-C gene of Salmonella typhi and Shigella dysenteriae using PCR and the result was characterized by 2% agarose gel electrophoresis. The primer pair of Shigella dysenteriae was able to amplified the DNA with fragment band at ± 95 pb, ± 700 pb and ± 1000 pb at annealing temperature 56°C. The primer pair of Salmonella typhi was able to amplified the DNA with fragment band at ± 95 pb at annealing temperature 56°C.
Item Type: | Thesis (Sarjana) |
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Additional Information: | 1) Dr. Muktiningsih Nurjayadi, M.Si 2) Dr. Fera Kurniadewi, M.Si |
Subjects: | Sains > Kimia |
Divisions: | FMIPA > S1 Kimia |
Depositing User: | sawung yudo |
Date Deposited: | 23 Mar 2022 02:11 |
Last Modified: | 23 Mar 2022 02:11 |
URI: | http://repository.unj.ac.id/id/eprint/25103 |
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