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產(chǎn)品信息

貨號	產(chǎn)品名稱	規(guī)格	價格/元
TNP92110	EZ-Tn5 Transposase/EZ-Tn5轉(zhuǎn)座酶	10 units	6418
EZI982K	EZ-Tn5? <KAN-2> Insertion Kit/EZ-Tn5? <KAN-2>插入試劑盒	10 rxns	6950
EZI921T	EZ-Tn5? <TET-1> Insertion Kit EZ-Tn5? <TET-1>插入試劑盒	10 rxns	6999
EZI912D	EZ-Tn5? <DHFR-1> Insertion Kit/EZ-Tn5? <DHFR-1>插入試劑盒	10 rxns	7060
EZI03T7	EZ-Tn5? <T7/KAN-2> Promoter Insertion Kit/EZ-Tn5? <T7/KAN-2>啟動子插入試劑盒	10 rxns	7312
EZI011RK	EZ-Tn5? <R6Kγori/KAN-2> Insertion Kit/EZ-Tn5? <R6Kγori/KAN-2>插入試劑盒	10 rxns	7517
CIS40025	CopyCutter? Induction Solution/CopyCutter?誘導試劑	25 mL	856

產(chǎn)品簡介

       Transposons are mobile DNA sequences found in the genomes of prokaryotes and eukaryotes. Transposon tagging has long been recognized as a powerful research tool for randomly   distributing primer binding sites, creating gene“knockouts”, and introducing a physical tag or a genetic tag into large target DNAs. One frequently used transposition system is the Tn5 system isolated from gram-negative bacteria. Though a naturally occurring transposition system, the Tn5 system can be readily adapted for routine use in research laboratories for the following reasons:

 1) Tn5 transposase is a small, single subunit enzyme that has been cloned and purified to high specific activity.

 2) Tn5 transposase carries out transposition without the need for host cell factors. 

 3) Tn5 transposon insertions into target DNA are highly random.

 4) Tn5 transposition proceeds by a simple“cut and paste”process. Although the chemistry is unique, the result is similar to using a restriction endonuclease, with random sequence specifi city, accompanied by a DNA ligase activity.

 5) Tn5 transposase will transpose any DNA sequence contained between its short    9 basepair Mo saic End (ME) Tn5 transposase recognition sequences.

       In 1998 Goryshin and Reznikoff1demonstrated that a fully functional Tn5 transposition system could be reconstituted in vitro. Additionally, the transposition efficiency of this system has been increased more than 1,000-fold compared to wild-type Tn5 by introducing mutations in the transposase gene and in the 19-bp Tn5 ME transposase recognition sequence.

        Lucigen’s EZ-Tn5 Transposon Tools (kits and reagents) are based on the hyperactive Tn5 transposition system developed by Goryshin and Reznikoff.

優(yōu)點：

        Insert a kanamycin, tetracycline, or DHFR selectable marker into any DNA sequence in vitro

        Skip primer walking - simplify Sanger sequencing of large DNA inserts

        Speed functional analysis without subcloning - create libraries of random mutants from purified DNA

        Minimize insertion bias with the hyperactive Tn5 system, known for highest level of randomness

組成成分：

               EZ-Tn5? Transposase 10 U ：儲存在-20℃

               EZ-Tn5? <R6Kγori/KAN-2> Transposon：儲存在-20℃

               EZ-Tn5? 10X Reaction Buffer：儲存在-20℃

               EZ-Tn5? 10X Stop Solution:儲存在-20℃

               KAN-2 FP-1 Forward Primer:儲存在-20℃

               R6KAN-2 RP-1 Reverse Primer:儲存在-20℃

               pUC19/3.4 Control Target DNA:儲存在-20℃

               Sterile Water:儲存在-20℃

數(shù)據(jù)：

 

Figure 1. The process for generating DNA sequencing templates using an EZ-Tn5 Insertion kit. 

 技術參數(shù)

產(chǎn)品優(yōu)點- Insert a kanamycin, tetracycline, or DHFR selectable marker into any DNA sequence in vitro

- Skip primer walking - simplify Sanger sequencing of large DNA inserts

- Speed functional analysis without subcloning - create libraries of random mutants from purified DNA

- Minimize insertion bias with the hyperactive Tn5 system, known for highest level of randomness

產(chǎn)品應用- Introduce the R6Kγori into any plasmid and/or cloning vector.

- Propagate vectors from non-E. coli species in E. coli. Randomly insert the EZ-Tn5 <R6Kγori/KAN-2> Transposon into any foreign vector, transform an E. coli pir+ or E. coli pir-116 strain and select on kanamycin plates.

- Propagate genomic DNA fragments from any species as independently replicating plasmids in E. coli . Randomly insert the EZ-Tn5 <R6Kγori/KAN-2> Transposon in vitro into self-ligated genomic DNA fragments, transform an E. coli pir+ strain and select on kan