Isolation and cloning of human NQO1 promoter in pGL3 basic vector
Malaria is a major public health problem caused by Plasmodium falciparum, a parasite that infects red blood cells. Recently, several polyphenolic compounds have been reported capable of preventing the progression of malaria parasite. This observation may be related to NAD (P) H: quinon oxidoreductas...
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my.utm.122872011-04-14T09:44:43Z http://eprints.utm.my/id/eprint/12287/ Isolation and cloning of human NQO1 promoter in pGL3 basic vector Chinigarzadeh, Asma RZ Other systems of medicine Malaria is a major public health problem caused by Plasmodium falciparum, a parasite that infects red blood cells. Recently, several polyphenolic compounds have been reported capable of preventing the progression of malaria parasite. This observation may be related to NAD (P) H: quinon oxidoreductase: a flavoprotein responsible for catalyzing two-electron reduction and detoxification of quinones and their derivatives. In this study the 2123 bp of the 5` upstream of the first transcription start site was successfully isolated. Based on the bioinformatic program, several regulatory regions such as Antioxidant Response Element (ARE) may be responsible for the direct regulation of polyphenols on this enzyme. It was predicted at -477 from the first transcription start site. Upon isolation, this fragment was used in a cloning process into the pGL3 Basic vector and transformed to E.coli DH5? competent cells 2010-12 Thesis NonPeerReviewed Chinigarzadeh, Asma (2010) Isolation and cloning of human NQO1 promoter in pGL3 basic vector. Masters thesis, Universiti Teknologi Malaysia, Faculty of Bioscience and Bioengineering. |
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Malaria is a major public health problem caused by Plasmodium falciparum, a parasite that infects red blood cells. Recently, several polyphenolic compounds have been reported capable of preventing the progression of malaria parasite. This observation may be related to NAD (P) H: quinon oxidoreductase: a flavoprotein responsible for catalyzing two-electron reduction and detoxification of quinones and their derivatives. In this study the 2123 bp of the 5` upstream of the first transcription start site was successfully isolated. Based on the bioinformatic program, several regulatory regions such as Antioxidant Response Element (ARE) may be responsible for the direct regulation of polyphenols on this enzyme. It was predicted at -477 from the first transcription start site. Upon isolation, this fragment was used in a cloning process into the pGL3 Basic vector and transformed to E.coli DH5? competent cells |
format |
Thesis |
author |
Chinigarzadeh, Asma |
author_facet |
Chinigarzadeh, Asma |
author_sort |
Chinigarzadeh, Asma |
title |
Isolation and cloning of human NQO1 promoter in pGL3 basic vector |
title_short |
Isolation and cloning of human NQO1 promoter in pGL3 basic vector |
title_full |
Isolation and cloning of human NQO1 promoter in pGL3 basic vector |
title_fullStr |
Isolation and cloning of human NQO1 promoter in pGL3 basic vector |
title_full_unstemmed |
Isolation and cloning of human NQO1 promoter in pGL3 basic vector |
title_sort |
isolation and cloning of human nqo1 promoter in pgl3 basic vector |
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2010 |
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http://eprints.utm.my/id/eprint/12287/ |
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