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Asimple,rapidprocedurefortheisolationofDNAforPCR

The polymerase chain reaction (PCR) is a method for amplifying specific segments of DNA defined by the small primers used to start the reaction. Using arbitrarily chosen 10-base primers, one can generate "random amplified polymorphic DNA" (RAPD) markers (Williams et al. 1991 Nucl. Acids Res. 18:6531-6535). These DNA fragments, separated by electrophoresis in an agarose gel, can be used as markers for studyi......阅读全文

DNA抽提

DNA抽提(主要内容如下)·   Working with DNA·   DNA Extraction from Bacteria and Other Organisms·   DNA Extraction f

Genomic DNA Extraction - PureLink™

实验概要The  PureLink™ Genomic DNA Purification Kit allows rapid and efficient  purification of genomic DNA. The kit is designed to efficiently

定量RT-PCR (Quantitative RT-PCR)

Application: Quantitative RT-PCR is used to quantify mRNA in both relative and absolute terms. It can be applied for the quantification of m

Isolation of Genomic DNA from Tissue Using ChargeSwitch® Technology

实验概要 The ChargeSwitch®  gDNA Mini and Micro Tissue Kits allow rapid and efficient purification  of genomic DNA from mini (10-25 mg) or

其它PCR方法

·         Standard PCR Protocol (Molecular Biology Techniques Manual)The followings are described in

反向PCR

主要内容如下:·         RT-PCR·         Competitive and Quantative

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

Isolation of micro-RNA (miRNA)

实验概要        This protocol utilizes the powerful guanidine isothiocyanate–phenol:chloroform extraction method which allows the

A simple, rapid procedure for the isolation of DNA for PCR

N.M. DuTeau and J.F. Leslie - Department of Plant Pathology, Throckmorton Hall, Kansas State University, Manhattan, KS 66506-5502The polymerase chain

An Ultra-fast method of DNA extraction from Neurospora

We have found that the DNA extraction procedure of Metzenberg and Baitch (Neurospora Newsl. 28:20)/Stevens and Metzenberg (Neurospora Newsl. 29:27) wh

DNA的酶学操作

DNA的酶学操作DNA Modifying Enzymes (Michael Blaber)Introduction to bacterial restriction/modification system. It provides very useful background knowl

SuperScript™ III One-Step RT-PCR System with Platinum® Taq High Fidelity

实验概要The  SuperScript™ III One-Step RT-PCR System with Platinum® Taq  High  Fidelity is designed for sensitive, high-fidelity end-p

Protocols for LCM preparation and analysis

Protocols for LCM preparation and analysis I. Preparation, LCM and RNA/DNA extraction of Frozen Tissue SectionsA. EmbeddingB. CuttingC.

Extraction of DNA From Plants Using Plant DNAzol® Reagent

实验概要Plant DNAzol® is an extra-strength-DNAzol® reagent (patent pending) specifically formulated for the isolation of genomic DNA from plants. The Plan

Standard Protocol For Up to 10 ml Whole Blood

实验概要The E.Z.N.A.®  Blood DNA Maxi Kit is designed for isolation of genomic DNA from up to  25 ml of fresh, whole blood treated with any comm

Extraction of DNA using DNAzol® Reagent

实验概要DNAzol®  Reagent (Genomic DNA Isolation Reagent) is a complete and ready-to-use  reagent for the isolation of genomic DNA from solid and

Competitive RT-PCR Strategy for Quantitative Evaluation -1

Competitive RT-PCR Strategy for Quantitative Evaluation of the Expression of Tilapia (Oreochromis niloticus) Growth Hormone Receptor Type IQuantizatio

转基因

DNA PreparationGene TransferEmbryo TransferTransgenic IdentificatioinOthersTransgenic Outline (University of Michigan Transgenic Animal Model Cor

An Integrative Procedure for Apoptosis Identification and Measurement-2

TroubleshootingCritical Steps(1) Don’t trypsinize cells for too long when collecting them.(2) Rotation speed should be no more than 1500 rpm during ce

结核杆菌的耐药机制及分子生物学检测方法进展(2

2 目前国内外应用于检测耐药结核杆菌的分子生物学方法随着分子生物学的发展,尤其是PCR技术的问世,检测耐药可以直接从基因入手,这样与传统的结核杆菌药敏试验相比,不仅大大缩短了检测周期,实现了自动化,而且也降低了生物实验室的危险性。耐药检测包括用PCR扩增基因组内携带的耐药性区域,和进行扩增产物的突变

ChIP using plant samples

实验概要 The  immunoprecipitation (IP) of cross-linked chromatin with antibodies  specific for certain histone modifications (chromatin &nb

质粒的小量制备

·         Standard (alkaline lysis) Mini-Prep (Goldberg Lab)Standard protocol for mini-prep and reci

质粒的小量制备

·         Standard (alkaline lysis) Mini-Prep (Goldberg Lab)Standard protocol for mini-prep and reci

siRNA Design Guidelines

Using siRNA for gene silencing is a rapidly evolving tool in molecular biology. There are several methods for preparing siRNA, such as chemical synthe

A novel method of growing fungi for DNA extraction

Preparation of fungi for DNA extraction typically involves growing cultures in liquid culture in Erlenmeyer flasks, Roux bottles or even microfuge tub

Culturing Mouse Embryonic Fibroblasts

MaterialsTrypsin (Gibco 25200-023)3T3 Medium:  500 mL DME (Invitrogen) + 50 mL FBS (Hyclone) + 5 mL 100x Pen/Strep2x Freezing Medium: 3T3 Medium

DNA Immunoprecipitation for the Determination of DNA-Binding Specificity

Andrea J. Gossett and Jason D. Lieb1Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA1Correspon

Gene splicing and mutagenesis by PCR-driven overlap extension

实验概要        Extension of overlapping gene segments by PCR is a simple, versatile technique for site-directed mutagenesis and g

High Throughput Isolation Of PCR Products Using ChargeSwitch® PCR Clean-Up

实验概要The ChargeSwitch®  PCR Clean-Up Kit allows rapid and efficient purification of PCR  products from salts, primers, dNTPs, and other non-n

Dynabeads® Streptavidin Trial Kit

实验概要Intended UseDynabeads®  Streptavidin are ideal for numerous applications, including  purification of proteins, nucleic acids purificatio