LigationOptimization
The following protocol can be used to optimize ligation conditions for difficult to clone (e.g. very large) fragments. The principle is to independently characterize the ligation kinetics of the vector and insert DNA fragments and then to combine them in optimal ratios. The final ligation is also performed in two stages to optimize the proportion of vector:insert heterodimers followed by a shift to low concentration ......阅读全文
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PCR引物
PCR Primer Design and Reaction Optimization (Molecular Biology Techniques Manual) PCR Primer Design (Newman Lab) PCR Primer Design (Eppendorf)Detail
PCR引物
PCR Primer Design and Reaction Optimization (Molecular Biology Techniques Manual) PCR Primer Design (Newman Lab) PCR Primer Design (Eppendorf)Detail
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Gene－Inactivation－in－the－Cyanobacterium－Synechococcus－sp.－PCC－7002－and...
Gene Inactivation in the Cyanobacterium Synechococcus sp. PCC 7002 and the Green Sulfur Bacterium Chlorobium tepidum Using In Vitro-Made DNA Const
Universal－RiboClone®－cDNA－Synthesis－System
Universal RiboClone® cDNA Synthesis SystemThe Universal RiboClone® cDNA Synthesis System contains the reagents required for the synthesis of double-st
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特点：检测小分子叠氮化物比CuAAC反应更快不需要铜离子，无毒性没有催化剂或者配体，因此无需大量的条件优化适合与四氮杂苯-反式环辛烯连接反应进行双标记方法 四氮杂苯-反式环辛烯连接反应（Tetrazine–trans- Cyclooctene Ligation，TCO）点击化学特点：快速点击化学反应
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This chapter describes a detailed protocol for genomic Southern blot analysis which can be used to detect transgene or endogenous gene sequences i
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The moss Physcomitrella patens is a long-standing model for studying plant development, growth and cell differentiation in particular. Interest in
Cloning－of－small－RNAs－with－5’－phosphate－and－3’－OH－ends2
3’ Adaptor Ligation and PurificationHeat shock the RNA by putting at 90°C for 30 seconds. Snap cool on ice.Set up the 3’Adaptor ligation reaction in a
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Chick－or－Mouse－embr...
实验概要The following procedure describes the procedure for whole mount staining of chick or mouse embryo’s. A similar procedure could be used for sta
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In addition, proficiency panel projects have demonstrated that even after an experiment was done and spots were counted, considerable variation can
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In a microcentrifuge tube prepare a solution of linear DNA (25-50ng) in deionized water or TE buffer (10-35µl).Add:10X ligation buffer 5µl,50% PEG 400
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Differential cDNA Screening ProceduresThe protocols listed refer to cDNA library construction and preliminary differential screening procedures. They
分享一些计算建模和仿真在类器官芯片技术中的具体应用论文
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反向PCR
主要内容如下：· RT-PCR· Competitive and Quantative RT-PCR· In Situ RT-PCR· RL-PCR· DNA Contamination· RT-PCR
Cloning－of－small－RNAs－with－5’－phosphate－and－3’－OH－ends01
IntroductionThe following protocol describes a procedure for the purification and cloning of miRNAs and other small RNAs in the 20-30 nucleotide size
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Introduction The most important aspect of our cloning vectors is that they are based on the E. coli F-factor replicon. It allows for strict
DNA指纹法
DNA Fingerprinting (David F. Betsch)the theory, procedures and applications · DNA Fingerprinting (Polyarylamide Gel) (Caltech)BAC DNA sample