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OGS186

Sigma-Aldrich

PSF-PA-PROMMCS - NO PROMOTER (MCS/POLYLINKER) PLASMID

plasmid vector for molecular cloning

别名:

cloning vector, expression vector, molecular cloning vector, plasmid, plasmid vector, snapfast vector, vector

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About This Item

UNSPSC代码:
12352200
NACRES:
NA.85

表单

buffered aqueous solution

分子量

size 3864 bp

菌种筛选

kanamycin

复制起点

pUC (500 copies)

肽切割

no cleavage

启动子


Promoter type: multiple cloning site

报告基因

none

运输

ambient

储存温度

−20°C

一般描述

PSF-PA-PROMMCS-no promoter (MCS/POLYLINKER) plasmid does not contain a promoter upstream of the main multiple cloning site. Instead this plasmid vector contains a short multiple cloning site (SalI to BstBI) in the same position that all of our promoters are normally inserted (flanked by Bgl2 sites). This region also contains an artificial poly-adenylation sequence upstream of the multiple cloning site to reduce background read-through from interfering with any promoter that you insert.

Promoter Expression Level:

应用

Cloning in a gene: PSF-PA-PROMMCS – no promoter (MCS/POLYLINKER) plasmid has been designed to be compatible with a range of cloning techniques. The multiple cloning site contains a range of standard commonly used restriction sites for cloning. Using these sites genes can be inserted using standard cloning methods with DNA ligase. Other methods such as ligase independent cloning (LIC) Gibson Assembly InFusionHD or Seamless GeneArt can also be used and because all of our plasmids are based on the same backbone the same method can be used for cloning into all of our catalogue vectors.

Multiple cloning site notes: There are a few important sites within the MCS. These include the NcoI site the XbaI site and the BsgI and BseRI sites. The NcoI site contains a start codon that is immediately downstream of both a Kozak and Shine-Dalgarno ribosomal binding site. These allow for optimal positioning of genes when the start codon is placed in this location. If this is not required and you wish to use a downstream site for gene cloning you can remove the NcoI site by cleaving the plasmid with KpnI.

The XbaI site contains a stop codon. This stop codon is positioned in a specific position in relation to the BsgI and BseRI sites that are immediately downstream. When either BseRI or BsgI cleave the plasmid they produce a TA overhang from the stop codon in the XbaI site that is compatible with all of our peptide tag plasmids cut with the same sites. BseRI and BsgI sites are non-palindromic and cleave a defined number of bases away from their binding site.

Whenever we clone a gene into our multiple cloning site we always position the start and stop codon in the same positions in the MCS. If the start and ends of the genes are not compatible with NcoI and XbaI we extend the sequence to the nearest external sites but keep the start and stop codons locations consistent.

序列

To view sequence information for this product, please visit the product page

分析说明

To view the Certificate of Analysis for this product, please visit www.oxgene.com

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说明
价格

储存分类代码

12 - Non Combustible Liquids

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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