Chemicon公司的CpGenomeDNAModificationKit的protocol修正
我用了快4个月这个试剂盒了，下面是一些总结出来的经验，我现在诱变每次都很成功了，呵呵：）1. 我溶NaOH的水PH值大概在6.5左右，所以我每次调Reagent I的时候3MNaO0H基本都要加150uL左右。2. 解链时用50度水浴15分钟。3. 加入Reagent I后，50度水浴16小时。4. 加入Reagent II和III后，室温孵育10分钟5. 第一次离心用9000 rpm 5分钟。6. 70%乙醇清洗3次，每次9000rpm 1 分钟，最后一次13000rpm2min。7. 加入20mM NaOH/90%EtOH后，反映5分钟。8. 不要去掉20mM NaOH/90%EtOH，直接加入90%乙醇后离心，9000rpm 1min9. 90%乙醇清洗2次，每次9000 rpm 1 min，最后一次13000rpm 3min10. PH 7.5 TE buffer 65度 溶解 15 minPS: 如果发现ＰＣＲ结果中M......阅读全文
Chemicon公司的CpGenome－DNA－Modification－Kit－的protocol修正
我用了快4个月这个试剂盒了，下面是一些总结出来的经验，我现在诱变每次都很成功了，呵呵：）1. 我溶NaOH的水PH值大概在6.5左右，所以我每次调Reagent I的时候3MNaO0H基本都要加150uL左右。2. 解链时用50度水浴15分钟。3. 加入Reagent I后，50度水浴16小时。4.
Fungal－Midi－DNA－Kit－Optional－protocol
实验概要This protocol is designed for isolation of genomic DNA from fresh, frozen, or dried specimens from fungal samples contains higher phenolic mat
Fungal－Midi－DNA－Kit－Protocol－for－Fresh/Frozen－Specimens
实验概要This protocol is suitable for most fresh or frozen tissue samples allowing more efficient recovery of DNA. However, due to the tremendous variat
Fastfilter－Plasmid－Midi－Kit－Spin－Protocol
实验概要The E.Z.N.A.TM Fastfilter Plasmid Midi Kit combines the power of HiBind® technology with the time-tested consistency of alkaline-SDS lysis of
Fastfilter－Plasmid－Midi－Kit－Vacuum/Spin－Protocol
实验概要The E.Z.N.A.TM Fastfilter Plasmid Midi Kit combines the power of HiBind® technology with the time-tested consistency of alkaline-SDS lysis of
Miniprep/Kitfree－highthroughput－protocol
BackgroundThis protocol is adapted from "Molecular Cloning: A Laboratory Manual", Second Edition, Sambrook, Fritsch, and Maniatis. It is a quick, inex
Chemicon－试剂盒的说明
TROUBLESHOOTINGNo products are visible in any lane.1. Potential Problem: PCR amplification is not initiated.Recommendations:a. Confirm that all PCR co
E.Z.N.A.®－Total－RNA－Midi－Kit－Protocol－DNase－I－digestion－Protocol
实验概要E.Z.N.A.® Total RNA Midiprep Kit provides a rapid and easy method for the isolation of up to 600 ug of total RNA from cultured eukaryotic cells,
E.Z.N.A.®－Plasmid－Maxi－Kit－vacuum－Protocol
实验概要This Protocol is designed to isolate 500-1200 ug of high Copy-Number plasmids or 50-400 ug of low Copy-Number Plasmids from 200 ml overnight c
E.Z.N.A.®－Plasmid－Maxi－Kit－Spin－Protocol
实验概要This Protocol is designed to isolate 500-1200 ug of high Copy-Number plasmids or 50-400 ug of low Copy-Number Plasmids from 200 ml overnight c
Streamlined－DNA－Extraction－Protocol
This method is derived from a procedure developed by Toby Bradshaw and the Poplar Molecular Genetics Cooperative. We have tested the procedure wit
Insect－DNA－Isolation－Protocol
实验概要The E.Z.N.A.® Insect DNA Kit is designed for efficient recovery of genomic DNA up to 60 kb in size from insects, arthropods, roundworms, flatw
E.Z.N.A.TM－Yeast－RNA－Kit－Spin－Protocol
实验概要The E.Z.N.A.® Yeast RNA Kit allows convenient isolation of high-quality total RNA from a wide variety of yeast species. Up to 2 x 107 log-phase cu
Methylene－Blue－DNA－staining－protocol
Methylene Blue DNA staining protocolProtocol:Load 2-5X the amount of DNA that would give bands of moderate intensity on an ethidium bromide stained ge
HP－Tissue－DNA－Midi－Protocol
实验概要The E.Z.N.A.® HP Tissue DNA Midi Kit is designed for efficient recovery of genomic DNA up to 60 kb in size from up to 500mg of tissue samples.
HP－Tissue－DNA－Maxi－Protocol
实验概要The E.Z.N.A.® HP Tissue DNA Maxi Kit is designed for efficient recovery of genomic DNA up to 60 kb in size from up to 2 grams of tissue samples.
E.Z.N.A.®－Total－RNA－Maxi－Kit－Protocol－for－Animal－Tissues
实验概要The E.Z.N.A.® Total RNA Maxi Kit uses HiBind® matrix spin-column technology to isolate up to 5 mg total cellular RNA from a variety of sources
Roche公司的RNase－Protection－Assay－(RPA)－protocol
Roche公司的RNase Protection Assay (RPA) Using DIG-Labeled RNA Probes下载网址：http://www.roche-applied-science.com/PROD_INF/BIOCHEMI/no1_03/PDF/p22_23.pdf还有一份
Automated－Extraction－－Normalized－DNA－Buccal－Kit
实验概要This section provides a general protocol for automated isolation of genomic DNA from human buccal cell swabs in a 96-well format using the Charg
E.Z.N.A.®－Total－RNA－Midi－Kit－Protocol－for－Eukaryotic－Cells－and－Tissues
实验概要E.Z.N.A.® Total RNA Midiprep Kit provides a rapid and easy method for the isolation of up to 600 ug of total RNA from cultured eukaryotic cells,
Vacuum/Spin－Protocol－for－Tissue－DNA－Extraction
实验概要The E.Z.N.A.® Tissue DNA Kit provides a rapid and easy method for the isolation of genomic DNA for consistent PCR and Southern analysis. Up to 3
DNA甲基化检测的序曲——亚硫酸氢盐转化
检测DNA甲基化的方法有很多种，在众多方法中，研究人员常常会使用到一项技术，那就是亚硫酸氢盐转化。DNA的亚硫酸氢盐处理将未甲基化的胞嘧啶转化成尿嘧啶，而甲基化的胞嘧啶保持不变。随后用测序、定量PCR和芯片等分析来比较处理和未处理DNA的序列，就能确定哪些碱基是甲基化的。尽管在理论上很简单，但亚硫酸
SQ－Blood－DNA－Mini－Protocol－for－Buffy－Coat
实验概要The buffy coat fraction of whole blood is enriched with WBC, and usually gives at least 5-fold more DNA than the same volume of blood. To prep
DNA－Saliva－Kit（唾液DNA提取试剂盒）使用说明
产品特点◎提取DNA纯度高，无抑制剂，A260/A280为1.7-1.9；◎产率高，同样的样本量提取的DNA更多；◎可用于唾液样本中DNA的提取，提取后的DNA可用于核酸检测使用；◎不含苯酚和氯仿等有毒溶剂，安全无毒。试剂盒组成 组分 50
细胞遗传学——原位杂交(ISH)
In Situ Hybridization· In Situ Hybridization (jsmith1@po-box.mcgill.ca)In situ hybridization, as the name suggests, is a method of localizing,
Maxiprep－of－plasmid－DNA－from－E.coli－protocol
Solutions/reagents:LB broth + selective marker50% sterile glycerolTEG(25mM Tris-Cl, 10mM EDTA, 50mM dextrose)20 mg/ml lysozyme10% SDS4M NaOHautoclaved
分光光度计测DNA含量的protocol
Turn on machine and wait for it to warm upWash glass cuvettes thoroughly before use and if 2 are used then make sure they are a ‘matching’ pair.For Sp
Protocol－for－Isolating－DNA－from－Blood－with－Nucleated－Red－blood－Cells
实验概要DNA isolation from fish or avian blood sample can be difficult because it contains nucleated red blood cells. E.Z.N.A. NRBC Blood DNA Kit is de
Vacuum/Spin－Protocol－for－Isolating－DNA－from－Blood－with－Nucleated－Red
实验概要DNA isolation from fish or avian blood sample can be difficult because it contains nucleated red blood cells. E.Z.N.A. NRBC Blood DNA Kit is de
iPrep™－GeneCatcher™－gDNA－Blood－Kit
实验概要The iPrep™ GeneCatcher™ gDNA Blood Kit allows rapid and automated extraction of genomic DNA (gDNA) from human blood including archived or poorly