Cloning of green fluorescence protein gene into binary vector
Green Fluorescent Protein (GFP) gene derived from the bioluminescent jellyfish, Aequoera victoria has been widely used in the field of molecular biology where it is utilized as reporter gene of many transformation events. The simplicity of this reporter gene has made it as one of the most stable rep...
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University Malaysia Sarawak, (UNIMAS)
2013
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Online Access: | http://ir.unimas.my/id/eprint/3213/7/Ruth%20Grace%20ft.pdf http://ir.unimas.my/id/eprint/3213/ |
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my.unimas.ir.32132023-08-28T07:35:46Z http://ir.unimas.my/id/eprint/3213/ Cloning of green fluorescence protein gene into binary vector Francis, Ruth Grace QR Microbiology SB Plant culture Green Fluorescent Protein (GFP) gene derived from the bioluminescent jellyfish, Aequoera victoria has been widely used in the field of molecular biology where it is utilized as reporter gene of many transformation events. The simplicity of this reporter gene has made it as one of the most stable reporter gene in plant transformation. Through times, a lot of researches have been done to study the applications of gfp gene in plants. In this project, a modification has been done on the genetic material of the binary vector, pGSA1131 which involved the removal of the destructive gus gene via restriction enzyme digestion followed by the blunting of gfp gene and vector ends, ligation, transformation of ligated vector and finally analysis of transformants. Based on the analysis, it is said that the cloning of the gfp gene obtained from plasmid MCB30 into binary vector pGSA1131 was not successful. University Malaysia Sarawak, (UNIMAS) 2013 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/3213/7/Ruth%20Grace%20ft.pdf Francis, Ruth Grace (2013) Cloning of green fluorescence protein gene into binary vector. [Final Year Project Report] (Unpublished) |
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QR Microbiology SB Plant culture Francis, Ruth Grace Cloning of green fluorescence protein gene into binary vector |
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Green Fluorescent Protein (GFP) gene derived from the bioluminescent jellyfish, Aequoera victoria has been widely used in the field of molecular biology where it is utilized as reporter gene of many transformation events. The simplicity of this reporter gene has made it as one of the most stable reporter gene in plant transformation. Through times, a lot of researches have been done to study the applications of gfp gene in plants. In this project, a modification has been done on the genetic material of the binary vector, pGSA1131 which involved the removal of the destructive gus gene via restriction enzyme digestion followed by the blunting of gfp gene and vector ends, ligation, transformation of ligated vector and finally analysis of transformants. Based on the analysis, it is said that the cloning of the gfp gene obtained from plasmid MCB30 into binary vector pGSA1131 was not successful. |
format |
Final Year Project Report |
author |
Francis, Ruth Grace |
author_facet |
Francis, Ruth Grace |
author_sort |
Francis, Ruth Grace |
title |
Cloning of green fluorescence protein gene into binary vector |
title_short |
Cloning of green fluorescence protein gene into binary vector |
title_full |
Cloning of green fluorescence protein gene into binary vector |
title_fullStr |
Cloning of green fluorescence protein gene into binary vector |
title_full_unstemmed |
Cloning of green fluorescence protein gene into binary vector |
title_sort |
cloning of green fluorescence protein gene into binary vector |
publisher |
University Malaysia Sarawak, (UNIMAS) |
publishDate |
2013 |
url |
http://ir.unimas.my/id/eprint/3213/7/Ruth%20Grace%20ft.pdf http://ir.unimas.my/id/eprint/3213/ |
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1775627152661676032 |
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13.211869 |