AgaroseGelElectrophoresis

实验概要Separating nucleic acid fragments by agarose gel electrophoresis.实验原理 Agarose gel electrophoresis remains the most widely used technique for separating nucleic acid fragments due to its ease of use, non-toxicity, and broad separation range. By varying agarose concentration, gel pore size can be controlled to separate nucleic acid molecules in a wide range of sizes. The migration......阅读全文

Agarose-Gel-Electrophoresis

实验概要Separating nucleic acid fragments by agarose gel electrophoresis.实验原理 Agarose  gel electrophoresis remains the most widely used technique for  sep

Agarose-gel-electrophoresis

General ProcedureCast a gelPlace it in gel box in running bufferLoad samplesRun the gelImage the gelCasting Gels0.7% agarose gel with 1kbp ladder in U

Standard-neutral-agarose-electrophoresis

Standard neutral agarose electrophoresisStandard agarose gels can be prepared using either TBE or TAE running buffers.You will need:Either 10 x TBE or

Agarose-Gel-Electrophoresis-of-DNA

1) Dissolve 1 g of agarose in 100 ml of 1X TAE or TBE buffer (gives a 1% gel). See note for making LMP agarose gel. 2) Cast the gel with the comb in p

Alkaline-agarose-gel-electrophoresis

Alkaline agarose gel electrophoresis (Sambrook et al., 1989)Alkaline agarose gels can be used to determine the size and quality of first and second st

DNA电泳(agarose胶)

DNA琼脂糖凝胶电泳             实验方法原理 利用DNA分子在琼脂糖凝胶中泳动时具有的电荷效应和分子筛效应。电荷效应是指DNA分子在高于等电点的pH溶液中带负电,在电场

ELECTROPHORESIS-OF-DNA-IN-AGAROSE-GELS

ELECTROPHORESIS OF DNA IN AGAROSE GELSA). AGAROSE CONCENTRATIONS:       Use 0.8% agarose (w/v) for high molecular weight DNA fragments, and 1 - 1.2% f

DNA电泳(agarose胶)

实验材料 DNA样品试剂、试剂盒 琼脂糖 电泳缓冲液溴化乙锭 上样缓冲液仪器、耗材 电泳仪电泳漕 透射紫外灯 胶带纸 紫外成像仪

DNA电泳(agarose胶)

DNA电泳可用于:(1)分离不同大小的DNA片段;(2)鉴定目的DNA片段;(3)纯化和回收DNA片段。实验方法原理利用DNA分子在琼脂糖凝胶中泳动时具有的电荷效应和分子筛效应。电荷效应是指DNA分子在高于等电点的pH溶液中带负电,在电场中向正极移动,且相同数量的双链DNA几乎具有等量的净电荷,能以

The-UnderAgarose-Migration-Assay

overviewThe Under-Agarose assay is a useful method for observing the response of a cell population to one or more chemoattractant sources. The behavio

Preparation-of-Agarose-Gels-for-DNA-separations

Weigh out the desired amount of agarose and place in an Erlenmeyer flask with a measured amount of electrophoresis buffer, e.g. for an 0.8% gel, add 0

Agarose-Gels-for-Single-Stranded-DNA

1. Prepare 50X TAE as:242 g Tris Base57.1 mL Glacial Acetic Acid100 mL 500 mM EDTA, pH 8.0600 mL ddH2OMix. Bring volume to 1 L. Autoclave.2. Mix the f

DNA-Purification-from-Agarose-Gels

1. Separate DNA fragments in an agarose gel cast with 0.5 mg/mL Ethidium bromide. Locate bands with a hand-held long-wave UV lamp.2. Slice the gel wit

High-Resolution-Agarose-Gel-Electrophoresis

实验概要Agarose gel  electrophoresis remains the most widely used technique for separating  nucleic acid fragments due to its ease of use, non-toxicity, a

Denaturing-Agarose-Gel-Electrophoresis-of-RNA

The overall quality of an RNA preparation may be assessed by electrophoresis on a denaturing agarose gel; this will also give some information about R

EGel®-CloneWell-Agarose-Gels

实验概要Instructions are  provided below for using the E-Gel®CloneWell pre-cast agarose gels with  the E-Gel® iBase™ Power System. For detailed instructio

Preparation-of-Yeast-DNA-Embedded-in-Agarose-Plugs

Preparation of Yeast DNA Embedded in Agarose PlugsAnja van Brabant(adapted from Iadonato, S. P., and A. Gnirke. 1996. RARE-cleavage analysis of YACs.

The-UnderAgarose-Migration-Assay2

F. Video Microscopy 1. The behavior of migrating cells may be filmed with an inverted microscope fitted with a CCD camera. 2. Determine the best magni

QUALITATIVE-ANALYSIS-OF-DNA-FRAGMENTATION-BY-AGAROSE-GEL-ELECTROPHORESIS

1. IntroductionNuclear morphology changes characteristic of apoptosis appear within the cell together with a distinctive biochemical event: the endonu

DNA电泳(agarose胶)操作方法

一、 试剂与材料:1、 琼脂糖2、 电泳缓冲液(1×TAE)3、 10mg/ml溴化乙锭4、 上样缓冲液5、 电泳仪和水平电泳漕6、 透射紫外灯7、 胶带纸 二、 操作方法 按1~2%的琼脂糖浓度(据DNA样品分子量不同而定)配胶100ml ↓ 置于微波炉内加热搅拌,至琼脂糖完全溶解

DNA凝胶电泳(DNA-agarose-gel-electrophoresis)

实验原理琼脂糖凝胶电泳是常用的用于分离、鉴定DNA、RNA分子混合物的方法,这种电泳方法以琼脂凝胶作为支持物,利用DNA分子在泳动时的电荷效应和分子筛效应,达到分离混合物的目的。DNA分子在高于其等电点的溶液中带负电,在电场中向阳极移动。在一定的电场强度下,DNA分子的迁移速度取决于分子筛效应,即分

RNA-analysis-on-nondenaturing-agarose-gel-electrophoresis

1. The following gel electrophoresis conditions are recommended:- use 1X TAE buffer instead of 1X TBE- use agarose gel in the concentration of 1.1%-1.

RNA-analysis-on-nondenaturing-agarose-gel-electrophoresis

实验概要RNA analysis on non-denaturing agarose gel electrophoresis实验步骤1. The following gel electrophoresis conditions are recommended:- use 1X TAE buffer

QUALITATIVE-ANALYSIS-OF-DNA-FRAGMENTATION-BY-AGAROSE-GEL-ELECTROPHORESIS2

3. Commentary    3.1. Background informationApoptosis is an innate mechanism of eukariotic cell suicide which plays a major role in many physiological

Antibody-Purification-using-Protein-A,-Protein-G,-or-Protein-L-Agarose

实验概要This  protocol is designed as a quick purification method for antibodies from  mammalian sera, ascites, and cell culture supernatants主要试剂 Protein

Antibody-Purification-using-Protein-A,-Protein-G,-or-Protein-L-Agarose

实验概要This protocol is designed as a quick purification method for antibodies from mammalian sera, ascites, and cell culture supernatants. It should

甲醛洋菜胶体电泳(formaldehydeagarose-gel-electrophoresis)

甲醛洋菜胶体电泳 (formaldehyde-agarose gel electrophoresis)甲醛是一种常用的RNA 变性剂。在进行甲醛洋菜胶体电泳分析时,必须先配制含有甲醛的洋菜胶体,RNA 也必须先以甲醛及formamide 进行变性处理,以确保其二度结构充分被打开。由于甲醛可能

琼脂糖凝胶电泳(agarose-gel-electrophoresis)介绍

主要试剂:核酸电泳缓冲液有三种,即Tris-硼酸(TBE)、Tris-乙酸(TAE)和Tris-磷酸(TPE).TBE与TPE缓冲容量高,DNA分离效果好,但TPE在DNA段回收时含磷酸盐浓度高,容易使DNA沉淀.TAE缓冲容量低,但价格较便宜,因而推荐选用TBE.缓冲液中的EDTA可螯合二价阳离子

琼脂糖凝胶电泳(agarose-gel-electrophoresis)检测DNA

原理: 琼脂糖是从海藻中提取出来的一种线状高聚物,可作为电泳支持物,适用于分离大小范围在0.2-50kb的DNA片段。DNA分子的迁移率与分子量的对数值成反比关系。观察其迁移距离,与标准DNA片段进行对照,就可获知该样品分子量大小。在质粒抽提过程中,由于各种因素的影响,使质粒DNA呈现超螺旋的共

双向琼脂糖凝胶电泳(agarose-gel-electrophoresis)实验

【实验目的】了解和掌握双向电泳技术,并学习用它来研究与DNA 复制相关的问题。【实验原理】DNA 分子有线状的,还有一些非线状的,如复制叉和重组DNA 结构。双向琼脂糖凝胶电泳技术就是被人们开发用以研究一些非线状DNA 分子的。双向琼脂糖凝胶电泳技术(2-D gel)实际上可分为两类:中性/中性