Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain

The purpose of this study were to design an optimized DNA extraction method which can produce optimum DNA yield and purity and to link the optimized DNA extraction method and PCR reaction in order to develop a porcine DNA detection system that can be commercialized for halal liaratn authentication o...

Full description

Saved in:
Bibliographic Details
Main Author: Ahmad Spain, Nur Arina
Format: Thesis
Language:English
Published: 2007
Subjects:
Online Access:https://ir.uitm.edu.my/id/eprint/99681/1/99681.PDF
https://ir.uitm.edu.my/id/eprint/99681/
Tags: Add Tag
No Tags, Be the first to tag this record!
id my.uitm.ir.99681
record_format eprints
spelling my.uitm.ir.996812024-08-02T10:19:32Z https://ir.uitm.edu.my/id/eprint/99681/ Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain Ahmad Spain, Nur Arina DNA. Deoxyribonucleic acids RM Therapeutics. Pharmacology RS Pharmacy and materia medica The purpose of this study were to design an optimized DNA extraction method which can produce optimum DNA yield and purity and to link the optimized DNA extraction method and PCR reaction in order to develop a porcine DNA detection system that can be commercialized for halal liaratn authentication of pharma-cosmeceutical products. There are two testing parameters used in this study and comparison between these two testing parameters and standard parameter of in house DNA extraction method was made in te1111s of efficiency to extract genomic DNA. This study was begun with in house DNA extraction using the all parameters as well the standard, followed by running nucleic acid gel electrophoresis to determine the size of the extracted genomic DNA. Next, the efficiency of all parameters used was confirmed with PCR assays. PCR assays will amplify the target DNA sequence, therefore its sensitivity and specificity is very important. At the final step, nucleic acid gel electrophoresis was nm to determine to size of the PCR products as well as to verify the efficiency of the two parameters. In conclusion, the two testing parameters used in this study have same efficiency as the standard parameter, and therefore can be used to replace the standard parameter. The results show that all pharma-cosmeceutical samples tested are free from porcine DNA. The efficiency of the optimized in house DNA extraction method is proven by the successive PCR assay. 2007 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/99681/1/99681.PDF Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain. (2007) Degree thesis, thesis, Universiti Teknologi MARA (Kampus Puncak Alam).
institution Universiti Teknologi Mara
building Tun Abdul Razak Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
url_provider http://ir.uitm.edu.my/
language English
topic DNA. Deoxyribonucleic acids
RM Therapeutics. Pharmacology
RS Pharmacy and materia medica
spellingShingle DNA. Deoxyribonucleic acids
RM Therapeutics. Pharmacology
RS Pharmacy and materia medica
Ahmad Spain, Nur Arina
Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain
description The purpose of this study were to design an optimized DNA extraction method which can produce optimum DNA yield and purity and to link the optimized DNA extraction method and PCR reaction in order to develop a porcine DNA detection system that can be commercialized for halal liaratn authentication of pharma-cosmeceutical products. There are two testing parameters used in this study and comparison between these two testing parameters and standard parameter of in house DNA extraction method was made in te1111s of efficiency to extract genomic DNA. This study was begun with in house DNA extraction using the all parameters as well the standard, followed by running nucleic acid gel electrophoresis to determine the size of the extracted genomic DNA. Next, the efficiency of all parameters used was confirmed with PCR assays. PCR assays will amplify the target DNA sequence, therefore its sensitivity and specificity is very important. At the final step, nucleic acid gel electrophoresis was nm to determine to size of the PCR products as well as to verify the efficiency of the two parameters. In conclusion, the two testing parameters used in this study have same efficiency as the standard parameter, and therefore can be used to replace the standard parameter. The results show that all pharma-cosmeceutical samples tested are free from porcine DNA. The efficiency of the optimized in house DNA extraction method is proven by the successive PCR assay.
format Thesis
author Ahmad Spain, Nur Arina
author_facet Ahmad Spain, Nur Arina
author_sort Ahmad Spain, Nur Arina
title Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain
title_short Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain
title_full Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain
title_fullStr Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain
title_full_unstemmed Optimization of in house lysis reagent concentration towards the performance of sus scrofa DNA detection system / Nur Arina Ahmad Spain
title_sort optimization of in house lysis reagent concentration towards the performance of sus scrofa dna detection system / nur arina ahmad spain
publishDate 2007
url https://ir.uitm.edu.my/id/eprint/99681/1/99681.PDF
https://ir.uitm.edu.my/id/eprint/99681/
_version_ 1806454663113867264
score 13.188404