首页 | 本学科首页   官方微博 | 高级检索  
   检索      

cDNA微阵列制作的优化
引用本文:黄宝俊,赵雨杰,徐惠绵,何群,张玉魁,徐莹莹,马佳明.cDNA微阵列制作的优化[J].遗传,2003,25(5):591-595.
作者姓名:黄宝俊  赵雨杰  徐惠绵  何群  张玉魁  徐莹莹  马佳明
作者单位:1. 中国医科大学附属第一医院肿瘤外科,沈阳,110001
2. 中国医科大学生物芯片中心,沈阳,110001
基金项目:辽宁省自然科学基金(2001101001)~~
摘    要:为了优化筛检cDNA微阵列中靶基因的最适长度、浓度及点样溶液的种类,设计持家基因betaactin和GAPDHRT PCR3对引物,产物长度在189~1078bp之间,以乙肝病毒DNA片段为阴性对照,扩增纯化后分别溶于3×SSC、50%DMSO及0.5mol/L碳酸盐缓冲液(pH=9.0)中,调整浓度分别为0.5μg/μL、1.0μg/μL和1.5μg/μL,比较上述不同条件的杂交结果。结果表明,杂交具有较好的特异性,阴性对照(乙肝病毒)和空白对照(点样溶液)均未见杂交信号;3种长度的同一靶基因杂交信号强度无明显差别(betaactinP=0.378;GAPDHP=0.866);3种点样溶液中以50%DMSO杂交信号最好,较强且均匀一致(P=0.0001),其余2种差异不显著(P=0.142);3种浓度靶基因杂交信号差异不显著(P=0.648),浓度高者信号略强。短片段靶基因(200bp左右)可获得与长片段靶基因(1000bp以上)一样较好的杂交信号,点样溶液以50%DMSO效果最好,靶基因浓度为0.5μg/μL时即可得到较好的杂交结果。

关 键 词:cDNA微阵列  靶基因  点样溶液  杂交
文章编号:0253-9772(2003)05-0591-05
修稿时间:2002年10月21

Optimization of cDNA Microarray Fabrication
Bao-Jun Huang,Yu-Jie Zhao,Hui-Mian Xu,Qun He,Yu-Kui Zhang,Ying-Ying Xu,Jia-Ming Ma.Optimization of cDNA Microarray Fabrication[J].Hereditas,2003,25(5):591-595.
Authors:Bao-Jun Huang  Yu-Jie Zhao  Hui-Mian Xu  Qun He  Yu-Kui Zhang  Ying-Ying Xu  Jia-Ming Ma
Institution:Oncology Department, The First Affiliated Hospital, China Medical University, Shenyang 110001, China. huang_bj@163.com
Abstract:To optimize and screen the most suitable target gene length,concentration and printing solution in cDNA microarray, housekeeping genes, such as beta actin and GAPDH, were selected as targets and hepatitis B virus gene as negative control. The RT-PCR primers that spanned at least one intron and whose products were at between 189 bp and 1078 bp were designed with primer premier 5.0, so did the hepatitis B virus gene PCR primer. After polymerase chain reaction, the products were purified with ethanol and dissolved in 3xSSC, 50% DMSO and 0.5 mol/L carbonate buffer(pH=9.0)respectively. The concentrations of target genes were adjusted at 0.5 microg/microL, 1.0 microg/microL and 1.5 microg/microL. The hybridization signals had a good specificity. No signal showed in either negative control (HBV) or blank control (printing solution only). There was no significant difference in target gene lengths. The P value of beta actin (189 bp,491 bp,974 bp) and GAPDH (227 bp,552 bp,1078 bp) was 0.378 and 0.866 respectively. There was no significant difference among concentrations(P=0.648),too. However, the higher the concentration was, the stronger the signals would be. Among the three kinds of printing solution, 50% DMSO was the best (P=0.0001), while the other two had no difference by multi-comparison (P=0.142). The target gene at length between 200 bp and 1000 bp has got the same hybridization signals.50% DMSO printing solution and the target gene concentration of 0.5 microg/microl are suitable for good hybridization.
Keywords:cDNA microarray  target gene  printing buffer
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号