OGS561
PSF-OXB18 - VERY STRONG E.COLI PROMOTER PLASMID
plasmid vector for molecular cloning
Sinónimos:
cloning vector, expression vector, molecular cloning vector, plasmid, plasmid vector, snapfast vector, vector
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About This Item
Código UNSPSC:
12352200
NACRES:
NA.85
Productos recomendados
formulario
buffered aqueous solution
mol peso
size 3858 bp
selección de bacterias
kanamycin
Origen de replicación
pUC (500 copies)
Escisión peptídica
no cleavage
Promotor
Promoter name: OXB18
Promoter activity: constitutive
Promoter type: bacterial
gen reportero
none
Condiciones de envío
ambient
temp. de almacenamiento
−20°C
Descripción general
PSF-OXB18 - VERY STRONG E.COLI PROMOTER PLASMID that allows the production of protein in bacteria. The plasmid contains our standard multiple cloning site downstream of the OXB18 promoter. We developed this promoter in house by modifying the RecA E. coli promoter so that it no longer repressed by LexA and also incorporates a series of mutations that make it slightly weaker. This is part of an extended product range of bacterial promoters with different transcriptional activities. OXB20 is the strongest in this range and OXB1 is the weakest. This plasmid vector does not require an inducing agent for activity.
Promoter Expression Level: This molecular cloning vector contains a very strong constitutive E. coli promoter that was derived from the RecA promoter by random mutagenesis. It is part of our constitutive bacterial promoter range. This promoter (OXB18) shows the very high levels of expression in the range with OXB1 showing the lowest level and OXB20 showing the highest level of expression. This vector require no inducing agent for expression.
Promoter Expression Level: This molecular cloning vector contains a very strong constitutive E. coli promoter that was derived from the RecA promoter by random mutagenesis. It is part of our constitutive bacterial promoter range. This promoter (OXB18) shows the very high levels of expression in the range with OXB1 showing the lowest level and OXB20 showing the highest level of expression. This vector require no inducing agent for expression.
Aplicación
Cloning in a gene: PSF-OXB18 - VERY STRONG E.COLI PROMOTER 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.
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.
Secuencia
To view sequence information for this product, please visit the product page
Nota de análisis
To view the Certificate of Analysis for this product, please visit www.oxgene.com
Producto relacionado
Referencia del producto
Descripción
Precios
Código de clase de almacenamiento
12 - Non Combustible Liquids
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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