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实验频道正文 用户登录 新用户注册 cDNA 作者:佚名 实验频道来源:中华基因网 点击数: 更新时间:2004-6-8 · cDNA Synthesis (Crawford Lab)mRNA can be converted into DNA (copy DNA, cDNA) by annealing oligo-dT to the 3 poly-A tail that occurs on all eukaryotic mRNA. After the dTs bind to the As, we will use the enzyme Reverse Transcriptase to read the RNA into DNA · Semi-solid Amplification of Plasmid cDNA Libraries (LTI)Protocol for Semi-solid Amplification of Plasmid cDNA Libraries · cDNA Synthesis (Promega)Provides detailed procedures for construction of cDNA library, including first strand and double-stranded cDNA synthesis from mRNA, and subsequent ligation into a suitable vector. · Protocol for First-strand cDNA Synthesis (Fermentas) · cDNA Library Construction (Michael Blabers Lab)Very useful guide and protocol for cDNA library construction · cDNA Library Construction (HMG)Detailed protocol for cDNA cloning · Differential cDNA Screening (Gerard Lazo)cDNA library construction and differential screeningcDNA Synthesis (Cungui Mao) Screening cDNA Clones by RNA In Situ Hybridization (Berkeley Drosophila Genome Project)The RNA in situ procedure described below is based on the protocol developed by Tautz and Pfeifle, but adapted to allow the screening of 96 RNA probes on whole-mount Drosophila embryos at the same time. · 32P Labeled Single-Stranded cDNA Synthesis (Jim Brown Lab) 32P labeled single-stranded cDNA (sscDNA) can be used in a usr/localiety of techniques; as a hybridization probe, for renaturation studies, or for eventual cloning. cDNA/AFLP (CWB Bachem)The protocol which follows gives a step-by-step description of cDNA-AFLP, a method for visualisation of differential gene expression 处理 SSI 文件时出错 处理 SSI 文件时出错 【评论】【进论坛看】【转入博客】 实验频道录入:生物编辑 责任编辑:生物编辑 上一篇实验频道: RNA电泳 下一篇实验频道: 引物延伸反应 【发表评论】【加入收藏】【告诉好友】【打印此文】【关闭窗口】 相关文章 最新热门 推荐文章 病毒DNA和RNA的简易纯化技术哺乳动物细胞中进行RNA干扰:哺乳动物细胞总RNA的分离RNA酶活性的控制mRNA的分离2%多聚甲醛固定剂配方二则细胞学技术细胞培养的一般技术血小板的活化、荧光染色与流血小板活化检测方法 · 免疫细胞表面抗原分子CD家族对照表· 所有的看家基因(housekeeping gene· 生物发光与化学发光专题· 生物发光和化学发光在生物技术中的· 重组DNA的分离、克隆与测序实验手册· RNAi和基因沉默的历史回顾· RNAi原理图解· RNAi术语表· siRNA设计指南· Methods for DNA sequencing · 通用电气医疗集团简介· 生物发光与化学发光专题· 生物发光和化学发光在生物技术中的· RNA干扰技术获得新突破· 蛋白质特性与分离纯化技术的选择· PCR实验指导与常见问题分析· RNAi原理FLASH演示· Extrachromosomal elements, plasm· Promoter analysis by saturation · 重组DNA的分离、克隆与测序实验手册 文章评论 (只显示最新10条。评论内容只代表网友观点,与本站立场无关!) 生物谷 | 网站介绍 | 网站地图 | 广告服务 | 帮助 关于我们 | 广告服务 | 战略伙伴 | 留言| 帮助信息| 联系方式 | 客户投诉 | 友情链接 | 网站地图 | 网站声明 | Bioon English 上海北岸信息技术有限公司 公司地址:上海龙吴路51号嘉源商务中心1#211室(200232) 生物谷网站 bioon.com © Copyright 2001 - 2006. All rights reserved. 备案号:沪ICP备05022939号 < 1 > < 2 >
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