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染色体免疫共沉淀(chip)

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识别和表征无义介导的mRNA降解过程中的序列模式

摘要 In both prokaryotes and eukaryotes nonsense mutations in a gene can enhance the decay rate or reduce the abundance of the mRNA transcribed from that gene and we call this process nonsense-m ...

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多核糖体mRNAs是酿酒酵母中mRNA无义介导降解途径的底物

摘要In eukaryotic cells premature termination of translation at nonsense codons has been implicated as the cause of a variety of posttranscriptional events including rapid mRNA decay in the cytoplasm or ...

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识别和表征加速降解包含早期翻译终止密码子的mRNAs的基因

In both prokaryotes and eukaryotes nonsense mutations in a gene can enhance the decay rate of the mRNA transcribed from that gene a phenomenon described as nonsense-mediated mRNA decay. In yeast the ...

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没有IRT的DNA样品或许会很脏

很多研究者因样品DNA很脏,转而求助于我们。问题样品主要集中在土壤、粪便和血液。样品富含腐植酸、多糖类、亚铁血红素和色素等,与DNA交联严重抑制下游PCR扩增等酶实验和测序。MO BIO拥有一项专利抑制因子去除技术®(IRT),应用在多款试剂盒上能高效去除抑制因子却极少影响DNA得率。这项技术真的有用吗?负责任的研究者需要看到实验数据。最近我们接到下面的一个问题:Q:你们有使用与不使用抑制 ...

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细胞短串联重复序列鉴定的重要性

短串联重复序列(short tandem repeat,STR),又称为微卫星DNA ,重复单位为2-6bp,重复次数10~60多次,在DNA复制过程中的滑动、复制、修复过程中滑动链与互补链的碱基错配,从而导致一个或几个重复单位的缺失或插入,形成STR的多态性,主要应用于遗传连锁图谱分析、家系鉴定、身份认证 ...

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单核苷酸多态性检测方法—SNapShot

SNP(Single Nucleotide Polymorphisms),即单核苷酸多态性,是指在基因组水平上由单个核苷酸的变异所引起的DNA序列多态性,它是人类可遗传的变异中最常见的一种,并作为第三代遗传标志。人体许多表型差异、对药物或疾病的易感性等等都可能与SNP有关,因此被广泛用于群体遗传学研究和疾病相关基因研究。目前,SNP检测技术已经很成熟,主要有以下几种检测方法:TaqMan探针法、H ...

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Methods for DNA isolation

A. Large scale double-stranded DNA isolationThe method used for the isolation of large scale cosmid and plasmid DNA is an unpublished modification (16) of an alkaline lysis procedure (1718) followed b ...

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Plasmid Mini-Prep

Objective:Mini-Prep procedure is used to isolate small plasmid DNA from bacteria while limiting contaminating proteins and genomic DNA. The plasmid quality is acceptable for restriction analysis seque ...

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Recovery plasmids from dead bacterial/plasmid

We store our all of our plasmids as bacterial host stocks at -80 stored in 7% DMSO. Such stocks are very long-lived giving robust bacterial growth even after 10-15 years. However occasionally we hav ...

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Purification of Plasmid from 50 ml-culture

1. Shake E. coli harboring plasmid at 37 C overnight in 50 ml of TB containing appropriate antibiotics. (when using ampicillin addition of the antibiotics to 100-200 ug/ml rather than usual 50 ug/ml m ...

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C10311 Cell-Light TM EdU 流式细胞仪 检测说明书

锐博生物新的EdU荧光标记技术,能够方便、快速、准确的检测研究细胞的增殖、周期、凋亡、活性、分化、迁移及示踪。详细使用说明请见下面的PDF文档!C10311 Cell-Light TM EdU 流式细胞仪 检测说明书.pdf需要订购相关产品请填好下面的合同和信息卡发到:sales-cd@ribobio.com!EdU&EU 订购信息卡.xlsRibobio 2010年购销合同.doc ...

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PEG Preparation of Plasmid DNA(聚乙二醇制备质粒)

You will need 3 basic solutions:-

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Reverse SAGE (rSAGE)

Jian Yu ( Email: jianyu@jhmi.edu)Last edited on May 1 2000OverviewThis protocol was developed in Kinzler/Vogelstein laboratories to isolate cDNA fragments corresponding to novel SAGE tags that do not ...

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Map-Based Cloning(图位克隆技术)

Map-Based Cloning of KAM2

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Mini-preps

IntroductionExtraction and purification of plasmid DNA from E.coli can be performed on a small scalewhere DNA is extracted from just 1-2 ml of bacterial culture (mini-prep) or from much larger volumes ...

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Bacterial Transformation(细菌转化)

IntroductionTransformation is a technique to introduce DNA into bacterial cells. There are many variations on a common theme but the key points are listed below. Check details with supplier of compete ...

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染色质 免疫沉淀 反应

Chromatin Immunoprecipitation Protocols. ChIP assay. Protocols and Methods for chromatin IP.CHROMATIN IMMUNOPRECIPITATION (CHIP) PROTOCOL FOR YEAST PDF - http://research.stowers-institute.org/jeg/200 ...

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