Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene

碩士 === 國立成功大學 === 材料科學及工程學系 === 104 === In this research, we developed a lateral-flow immunoassay combined with primer extension (PEXT) method for SNP genotyping of tmigd1 gene in Tsaiya duck (Anas platyrhynchos), and discussed the effects of experiment parameters on both signal specificity and inte...

Full description

Bibliographic Details
Main Authors: Chih-WeiLin, 林志韋
Other Authors: Jui-Chao Kuo
Format: Others
Language:zh-TW
Published: 2016
Online Access:http://ndltd.ncl.edu.tw/handle/26596697514819368124
id ndltd-TW-104NCKU5159018
record_format oai_dc
spelling ndltd-TW-104NCKU51590182017-10-01T04:30:03Z http://ndltd.ncl.edu.tw/handle/26596697514819368124 Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene tmigd1基因單核苷酸多型性之乾式生物檢測試紙系統 Chih-WeiLin 林志韋 碩士 國立成功大學 材料科學及工程學系 104 In this research, we developed a lateral-flow immunoassay combined with primer extension (PEXT) method for SNP genotyping of tmigd1 gene in Tsaiya duck (Anas platyrhynchos), and discussed the effects of experiment parameters on both signal specificity and intensity. According to our result, the optimal setup is 1mM Mg2+ with 0.12μg streptavidin. Increasing the amount of PCR product or PEXT reaction cycle number can enhance the signal without observable change of signal specificity. To validate the reproducibility, we perform the test with additional 6 DNA samples. We were able to obtain specific signals from all the DNA samples, but the signal intensities were be affected by the concentration of PCR prducts. According to our calculation, time requirement of this method is about 40 minutes, and the cost for 1 strip test is about 38.5 NTD. Jui-Chao Kuo Hsiu-Lin Huang 郭瑞昭 黃秀琳 2016 學位論文 ; thesis 178 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 國立成功大學 === 材料科學及工程學系 === 104 === In this research, we developed a lateral-flow immunoassay combined with primer extension (PEXT) method for SNP genotyping of tmigd1 gene in Tsaiya duck (Anas platyrhynchos), and discussed the effects of experiment parameters on both signal specificity and intensity. According to our result, the optimal setup is 1mM Mg2+ with 0.12μg streptavidin. Increasing the amount of PCR product or PEXT reaction cycle number can enhance the signal without observable change of signal specificity. To validate the reproducibility, we perform the test with additional 6 DNA samples. We were able to obtain specific signals from all the DNA samples, but the signal intensities were be affected by the concentration of PCR prducts. According to our calculation, time requirement of this method is about 40 minutes, and the cost for 1 strip test is about 38.5 NTD.
author2 Jui-Chao Kuo
author_facet Jui-Chao Kuo
Chih-WeiLin
林志韋
author Chih-WeiLin
林志韋
spellingShingle Chih-WeiLin
林志韋
Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene
author_sort Chih-WeiLin
title Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene
title_short Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene
title_full Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene
title_fullStr Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene
title_full_unstemmed Dry-Reagent Strip Biosensor for Single Nucleotide Polymorphism in tmigd1 Gene
title_sort dry-reagent strip biosensor for single nucleotide polymorphism in tmigd1 gene
publishDate 2016
url http://ndltd.ncl.edu.tw/handle/26596697514819368124
work_keys_str_mv AT chihweilin dryreagentstripbiosensorforsinglenucleotidepolymorphismintmigd1gene
AT línzhìwéi dryreagentstripbiosensorforsinglenucleotidepolymorphismintmigd1gene
AT chihweilin tmigd1jīyīndānhégānsuānduōxíngxìngzhīgānshìshēngwùjiǎncèshìzhǐxìtǒng
AT línzhìwéi tmigd1jīyīndānhégānsuānduōxíngxìngzhīgānshìshēngwùjiǎncèshìzhǐxìtǒng
_version_ 1718541837392674816