HowtouseBasicLocalAlignmentSearchTool(BLAST)

DescriptionThe BLAST algorithm was developed as a way to perform DNA and protein sequence similarity searches by an algorithm that is faster than FASTA but considered to be equally as sensitive. Both of these methods follow a heuristic (tried-and-true) method that almost always works to find related sequences in a database search, but does not have the underlying guarantee of an optimal ......阅读全文

How-to-use-Basic-Local-Alignment-Search-Tool-(BLAST)

DescriptionThe BLAST algorithm was developed as a way to perform DNA and protein sequence similarity searches by an algorithm that is faster than FAST

A-Collection-of-PlantSpecific-Genomic-Data-and-Resources-at-NCBI

The National Center for Biotechnology Information (NCBI) provides a data-rich environment in support of genomic research by collecting the biologi

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1) Turn on the counter by pulling out the on/off button. You need to do this at least 10 min before use to obtain sufficient vacuum.Usually put 0.2 ml

How-to-Import-Medline-Search-Result-(DUMC-OVID)-in-Reference-Manager

If you would like to print this page, please use the printer inRm. 221 since printing through those printers in the computer rooms will be UNBELIEVABL

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For ionisation to take place at all, chemical reaction between the sample and the reagent gas must be exothermic. The grater the heat of the reaction,

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BASIC THEORY AND USE OF GC-MSbyDr. Eugenia SobolevaContent1.  Introduction.2.  GC-MS systems and components.3.  Vacuum system3.1.  Rotary pump3.2.  Di

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RNAi target selection rules:Targeted regions on the cDNA sequence of a targeted gene should be located 50-100 nt downstream of the start codon (ATG).S

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Sequence - Evolution - FunctionComputational Approaches in Comparative GenomicsbyEugene V. KooninNational Center for Biotechnology Information, Bethes

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What is degenerate PCR?   Degenerate PCR is in most respect identical to ordinary PCR, but with one major difference. Instead of using specific PCR pr

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Identify reuses of GEO datasetsAimThe aim of this protocol is to collect data on the reuses of datasets in the published literature. This particular p

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Degenerate PCR is in most respects identical to ordinary PCR, but with one major difference. Instead of using specific PCR primers with a given sequen

RNAi技术专有名词(2)

21.Homologous Chromosome:同源染色体一对染色体,分别来自父本和母本,染色体上有着相同的线性基因序列。 22.Recombinant Clone:重组克隆将不同来源的DNA片段合成在一个DNA分子中,这种技术称为重组,得到的分子为重组克隆。 23.Ribonucleic

Blast基本介绍

什么是BLAST?BLAST (Basic Local Alignment Search Tool)是一套在蛋白质数据库或DNA数据库中进行相似性比较的分析工具。BLAST程序能迅速与公开数据库进行相似性序列比较。BLAST结果中的得分是对一种对相似性的统计说明。BLAST 采用一种局部的算法获得两

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Gastrulation has been celled "the most important time of your life" (Lewis Wolpert); without it you would be flat like a pancake! Vertebrate gastrulat

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The i PhyClassifier is an internet-based research tool for quick identification and classification of diverse phytoplasmas. The i PhyClassifier simu

siRNA数据库与设计工具

siRNA DatabaseSearchable database of Silencer ™ Validated and Pre-designed siRNAs to >34,000 human, mouse, and rat targets. All siRNAs in the database

基因表达轮廓(gene-expressed-profile)技术3

电子杂交即虚拟的RNA杂交(Virtual northern blots)。用已知的EST序列为起始序列,采用BLAST(Basic Local Alignment Search Tool,BLAST)检索程序检索数据库中与其同源或有部分重叠的EST序列,以分别确定EST是属于已知基因还是已

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Basic-PCR

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第八章:常用引物设计工具大集合

Oligo 6作为目前最好、最为专业的引物设计软件,Oligo 的功能很强大,他主要功能有:普通引物对的搜索、测序引物的设计、杂交探针的设计以及评估「引物对」质量的功能。如何使用Oligo6 请参看:「两分钟教你学会 Oligo 7」BLASTBLAST(Basic Local Alignment

常用引物设计工具大集合

Oligo 6作为目前最好、最为专业的引物设计软件,Oligo 的功能很强大,他主要功能有:普通引物对的搜索、测序引物的设计、杂交探针的设计以及评估「引物对」质量的功能。如何使用Oligo6 请参看:「两分钟教你学会 Oligo 7」BLASTBLAST(Basic Local Alignment

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The Transmission Electron Microscope (TEM) (HEI)An explanation of how the TEM works.  TEM Specimen Preparation (HEI)  Serial Sectioning (Walter Steffe

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eBioscience公司Luminex液相蛋白芯片检测试剂——ProcartaPlex可以为您的生物学研究提供各种多因子检测方案,包括细胞因子、生长因子、趋化因子和其他蛋白。在选择试剂盒及操作时会遇到很多问题,现将常见问题及答复汇总如下,供您参考: 如果不小心将整个试剂盒保存在-20°C. 这个试

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METTLER TOLEDO is pleased to announce their series of one-day training courses, which are designed to familiarize users with thermal analysis theo

USE-诱变实验

            实验材料 带 mutS 表型(例如 BMH71-18) 的转化用大肠杆菌感受态 带 mut+表型的转化用大肠杆菌感受态 试剂、试剂盒

USE-诱变实验

本方法中,两条寡核苷酸引物杂交到变性重组质粒 DNA 双链的同一条链上。一条引物(诱变引物)携带一个拟引进靶 DNA 序列的突变,第二条引物携带一个能破坏质粒单一限制酶位点的突变。本实验来源于分子克隆实验指南(第三版)下册,作者:〔美〕J. 萨姆布鲁克 D.W. 拉塞尔。实验材料带 mutS 表型(

USE-诱变实验

实验材料 带 mutS 表型(例如BMH71-18) 的转化用大肠杆菌感受态带 mut+表型的转化用大肠杆菌感受态试剂、试剂盒 退火缓冲液贮存液合成缓冲液噬菌体 T4DNA 连接酶噬菌体 T4DNA 聚合酶或测序酶单一位点的限制性内切核酸酶琼脂糖凝胶诱变引物选择引物质粒 DNA仪器、耗材 70°C