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实验频道正文 用户登录 新用户注册 DNA的诱变和甲基化 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 · In Vitro Mutagenesis Using Altered Sites (Bowtell Lab) In vitro Mutagenesis with dut ung single stranded DNA (Hahn Lab) · Site-directed Mutagenesis using PCR (Lazo Lab)PCR site-directed methods allow site-specific mutations to be incorporated in virtually any double-stranded plasmid; eliminating the need for M13-based vectors or single-stranded rescue.· Site-directed mutagenesis (Dr. Chastain)· Site Directed Mutagenesis Using the Ung-Dut System (Bowtell Lab)· Oligonucleotide-directed mutagenesis (Kunkel method) (Jeff NEwman)· Site-directed Mutagenesis (Promega)For generation and selection of oligonucleotide-directed mutants· Site Directed Mutagenesis Using the Ung-Dut System (PMCI Research)· Nested Deletions (Bowtell Lab)Nested Deletions using exonuclease-III and mung bean nuclease· Deletion Mutagenesis (Promega)For construction of plasmid or M13 subclones containing progressive unidirectional deletions of inserted DNA, Including methods for DNA preparation, vector digestion, exonuclease deletion, ligation, transformation...· ExoIII/S1 Deletion (Fermentas)For construction of plasmid or M13 subclones with nested unidirectional deletions. The method is applicable for DNA sequencing, mapping of boundaries of regions involved in genetic control, DNA/protein interaction sites, or protein domains.· Exo/S1 Deletion Series (Vesicle Trafficking) Four Primer Mutagenesis (PDF) (Templenton Lab)A PCR-based mutagenesis, based on Sarkar and Sommer, but with no ligation required. · Nested Deletions Using Exonuclease-III and Mung Bean Nuclease (PMCI Research) · In vitro Mutagenesis Using Altered Sites (PMCI Research) · Unidirectional deletions (erase-a-base) (Crawford Lab) Design of Mutagenic Oligonucleotides (Promega)Methylation analysis· Bisulfite Treatment of DNA (Issa Lab)· Methylation-Sensitive PCR (MSP) (Issa Lab)· Bisulfite-PCR (for restriction and/or sequencing) (Issa Lab)· Southern Blot Analysis (Issa Lab)· Methylated CpG Island Amplification (MCA) (Issa Lab)· DNA-Methyltransferase Assay (Issa Lab)· Bisulfite Modification (TTO)Modify DNA with bisulfite for methylation analysis 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: T载体的制作和应用 下一篇实验频道: DNA微序列技术 【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 免疫组化染色过程中存在的问常用核酸和氨基酸代码动物模型的设计原则和注意事PCR常见问题总汇如何确定RNA质量的经验谈PCR引物设计的11条黄金法则蛋白纯化经验指南TA克隆常见问题分析及其解决免疫组化实验过程中的要点和核酸的抽提---mRNA的分离技巧 · 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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