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本文引用的文献

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2
Oligonucleotide fingerprint identification for microarray-based pathogen diagnostic assays.基于微阵列的病原体诊断检测的寡核苷酸指纹识别
Bioinformatics. 2007 Jan 1;23(1):5-13. doi: 10.1093/bioinformatics/btl549. Epub 2006 Oct 26.
3
The effects of different sample labelling methods on signal intensities of a 60-mer diagnostic microarray.不同样本标记方法对60聚体诊断微阵列信号强度的影响。
J Virol Methods. 2006 Jun;134(1-2):36-40. doi: 10.1016/j.jviromet.2005.11.017. Epub 2006 Jan 4.
4
[Comparison of two amine-modified chemical platforms for DNA microarray preparation].[用于DNA微阵列制备的两种胺修饰化学平台的比较]
Di Yi Jun Yi Da Xue Xue Bao. 2005 Jul;25(7):794-8.
5
Multipathogen oligonucleotide microarray for environmental and biodefense applications.用于环境和生物防御应用的多病原体寡核苷酸微阵列
Biosens Bioelectron. 2004 Nov 1;20(4):684-98. doi: 10.1016/j.bios.2004.04.030.
6
Molecular biology and DNA microarray technology for microbial quality monitoring of water.用于水微生物质量监测的分子生物学与DNA微阵列技术
Crit Rev Microbiol. 2004;30(3):145-72. doi: 10.1080/10408410490435142.
7
Immobilized probe and glass surface chemistry as variables in microarray fabrication.固定化探针和玻璃表面化学作为微阵列制造中的变量。
BMC Genomics. 2004 Aug 4;5(1):53. doi: 10.1186/1471-2164-5-53.
8
Oligonucleotide microarrays in microbial diagnostics.用于微生物诊断的寡核苷酸微阵列
Curr Opin Microbiol. 2004 Jun;7(3):245-54. doi: 10.1016/j.mib.2004.04.005.
9
Nucleic acid amplification strategies for DNA microarray-based pathogen detection.基于DNA微阵列的病原体检测的核酸扩增策略。
Appl Environ Microbiol. 2004 May;70(5):3047-54. doi: 10.1128/AEM.70.5.3047-3054.2004.
10
A modified restriction display PCR method in sample-labelling of DNA microarray.一种用于DNA微阵列样品标记的改良限制性显示PCR方法。
J Virol Methods. 2003 Dec;114(1):71-5. doi: 10.1016/j.jviromet.2003.09.013.

玻璃表面和探针GC含量对60聚体诊断微阵列信号强度的影响。

The effects of glass surfaces and probe GC content on signal intensities of a 60-mer diagnostic microarray.

作者信息

Mo Xiaoyang, Wu Qinghua, Hu Junjian, Ma Wenli, Wei Min, Yuan Wuzhou, Wang Yuequn, Li Yongqin, Deng Yun, Wu Xiushan

机构信息

1The Center for Heart Development, Key Lab of MOE for Development Biology and Protein Chemistry, College of Life Sciences, Hunan Normal University, 410081 Changsha, Human.

2Key Lab of Biochip, Southern Medical University, 510515 Guangzhou, Guangdong, China.

出版信息

Ann Microbiol. 2008;58(2):313. doi: 10.1007/BF03175336.

DOI:10.1007/BF03175336
PMID:32226355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7097383/
Abstract

The effects of glass surfaces and probe GC content on signal intensities of a 60-mer diagnostic microarray were studied. Twelve virus-specific oligonucleotide probes for severe acute respiratory syndrome coronavirus (SARS-CoV) were divided into a high GC content group (≥ 50%) and a low GC content group (< 50%), and spotted onto four different chemically-modified glass surfaces: a poly-amine coating activated by 1,4-phenylene diisothiocyanate (Poly-Amine surface), an acrylic acid-co-acrylamide copolymer coating activated by 1-(3-dimethylamino propyl)-3-ethylcarbodiimide hydrochloride and N-hydroxysuccinimide (AACA-Copolymer surface), a commercial Corning CMT-GAPS amino surface, and a Telechem SuperAmine amino surface. RNA samples from cultured SARS-CoV strain were labelled using direct cDNA labelling with restriction display in a single colour format. The background-subtracted signal intensities were analysed using two-way analysis of variance. The effects of glass surfaces on background-subtracted signal intensities were significant (p=0.003). Multiple comparisons showed that differences existed mainly between the AACA-Copolymer surface and the other glass surfaces, and that the AACA-Copolymer surface had the highest background-subtracted signal intensity. The probe GC content had no significant effect on signal intensities in the narrow range of GC content represented (p=0.07). The results suggested that the AACA-Copolymer surface may be a novel choice of microorganism survey based on long oligonucleotide microarray.

摘要

研究了玻璃表面和探针GC含量对60聚体诊断微阵列信号强度的影响。将针对严重急性呼吸综合征冠状病毒(SARS-CoV)的12种病毒特异性寡核苷酸探针分为高GC含量组(≥50%)和低GC含量组(<50%),并点样到四种不同化学修饰的玻璃表面上:由1,4-亚苯基二异硫氰酸酯活化的聚胺涂层(聚胺表面)、由盐酸1-(3-二甲氨基丙基)-3-乙基碳二亚胺和N-羟基琥珀酰亚胺活化的丙烯酸-丙烯酰胺共聚物涂层(AACA-共聚物表面)、商业康宁CMT-GAPS氨基表面和Telechem SuperAmine氨基表面。使用单颜色格式的限制性显示直接cDNA标记法对培养的SARS-CoV毒株的RNA样本进行标记。使用双向方差分析对扣除背景后的信号强度进行分析。玻璃表面对扣除背景后的信号强度的影响具有显著性(p=0.003)。多重比较表明,差异主要存在于AACA-共聚物表面与其他玻璃表面之间,且AACA-共聚物表面具有最高的扣除背景后的信号强度。在所代表的GC含量窄范围内,探针GC含量对信号强度没有显著影响(p=0.07)。结果表明,基于长寡核苷酸微阵列,AACA-共聚物表面可能是微生物检测的一种新选择。