Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell

Nasopharyngeal carcinoma (NPC) is one of the major health problem in Malaysia, reported to be the fourth most common cancer among Malaysians and the third most common cancer among Malaysian men. The mechanisms which cause the disease is not fully understood because the understanding about NPC-associ...

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Main Author: Pithrianey Dyllarra, Fernandez
Format: Final Year Project Report
Language:English
English
Published: Universiti Malaysia Sarawak, (UNIMAS) 2018
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Online Access:http://ir.unimas.my/id/eprint/35111/1/PITHRIANEY%2024%20pgs.pdf
http://ir.unimas.my/id/eprint/35111/4/PITHRIANEY%20fulltext.pdf
http://ir.unimas.my/id/eprint/35111/
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spelling my.unimas.ir.351112024-02-23T03:18:54Z http://ir.unimas.my/id/eprint/35111/ Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell Pithrianey Dyllarra, Fernandez Q Science (General) QH301 Biology Nasopharyngeal carcinoma (NPC) is one of the major health problem in Malaysia, reported to be the fourth most common cancer among Malaysians and the third most common cancer among Malaysian men. The mechanisms which cause the disease is not fully understood because the understanding about NPC-associated gene is unclear and how ribosomal protein (RP) genes become part of it. In this study, human ribosomal protein S8 (uS8) gene is studied to find out whether or not the mutation of this gene is the cause of differential expression of the ribosomal protein gene which lead to NPC. The objective of this project is to isolate the sequence of uS8 gene in HK1 cell lines and to analyse the sequence of uS8 gene isolated from the HK1 cell lines. In this study, a set of primer is designed by using NCBI primer blast, Oligo Calc, and OligoAnalyzer 3.1. Then, gradient PCR is used to amplify the DNA of interest. However, both objectives are not achieved at the end of this project. There is no amplification of target gene from the gradient PCR as no band is observed from the gel visualization. To conclude, technical error must be reduced and to study about mutation analysis, biological replicates should be conducted instead of studying on one type of cell line only. Universiti Malaysia Sarawak, (UNIMAS) 2018 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/35111/1/PITHRIANEY%2024%20pgs.pdf text en http://ir.unimas.my/id/eprint/35111/4/PITHRIANEY%20fulltext.pdf Pithrianey Dyllarra, Fernandez (2018) Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell. [Final Year Project Report] (Unpublished)
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
English
topic Q Science (General)
QH301 Biology
spellingShingle Q Science (General)
QH301 Biology
Pithrianey Dyllarra, Fernandez
Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell
description Nasopharyngeal carcinoma (NPC) is one of the major health problem in Malaysia, reported to be the fourth most common cancer among Malaysians and the third most common cancer among Malaysian men. The mechanisms which cause the disease is not fully understood because the understanding about NPC-associated gene is unclear and how ribosomal protein (RP) genes become part of it. In this study, human ribosomal protein S8 (uS8) gene is studied to find out whether or not the mutation of this gene is the cause of differential expression of the ribosomal protein gene which lead to NPC. The objective of this project is to isolate the sequence of uS8 gene in HK1 cell lines and to analyse the sequence of uS8 gene isolated from the HK1 cell lines. In this study, a set of primer is designed by using NCBI primer blast, Oligo Calc, and OligoAnalyzer 3.1. Then, gradient PCR is used to amplify the DNA of interest. However, both objectives are not achieved at the end of this project. There is no amplification of target gene from the gradient PCR as no band is observed from the gel visualization. To conclude, technical error must be reduced and to study about mutation analysis, biological replicates should be conducted instead of studying on one type of cell line only.
format Final Year Project Report
author Pithrianey Dyllarra, Fernandez
author_facet Pithrianey Dyllarra, Fernandez
author_sort Pithrianey Dyllarra, Fernandez
title Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell
title_short Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell
title_full Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell
title_fullStr Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell
title_full_unstemmed Mutation Analysis of the Human Ribosomal Protein S8 (uS8) Gene in Nasopharyngeal Carcinoma (NPC) Cell
title_sort mutation analysis of the human ribosomal protein s8 (us8) gene in nasopharyngeal carcinoma (npc) cell
publisher Universiti Malaysia Sarawak, (UNIMAS)
publishDate 2018
url http://ir.unimas.my/id/eprint/35111/1/PITHRIANEY%2024%20pgs.pdf
http://ir.unimas.my/id/eprint/35111/4/PITHRIANEY%20fulltext.pdf
http://ir.unimas.my/id/eprint/35111/
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score 13.188404