OGS521

PSF-CMV-FMDV-KRYFP - FMDV IRES YFP REPORTER VECTOR

plasmid vector for molecular cloning

• Sinónimos: cloning vector, expression vector, molecular cloning vector, plasmid, plasmid vector, snapfast vector, vector
• Código UNSPSC: 12352200
• NACRES: NA.85

Propiedades

• formulario: buffered aqueous solution
• mol peso: size 5422 bp
• selección de bacterias: kanamycin
• Origen de replicación: pUC (500 copies)
• Escisión peptídica: no cleavage
• Promotor: Promoter name: CMV; Promoter activity: constitutive; Promoter type: mammalian
• gen reportero: YFP
• Condiciones de envío: ambient
• temp. de almacenamiento: −20°C

Descripción

Descripción general

This vector contains a CMV promoter that allows the expression of a transgene in mammalian cells. The plasmid also includes the internal ribosome entry site (IRES) from Foot and Mouth Disease Virus (FMDV) which allows two proteins to be translated from the same mRNA molecule. In this vector there is a yellow fluorescent protein (YFP) reporter gene after the IRES. FMDV IRES expression is often signficantly lower (typically 20-30 fold lower by total protein weight) than the gene upstream of the IRES. The reporter in this plasmid is called Kringle YFP and was developed by DNA2. 0.

Promoter Expression Level: <strong>Promoter and IRES Expression Level: </strong>This plasmid contains the mammalian CMV promoter to drive gene expression. We have tested all of our mammalian promoters in a range of cell types and CMV is consistently the strongest in those we have studied. However there are many reports of the CMV promoter demonstrating silencing by methylation in long-term culture. The IRES that is used to drive YFP expression from the CMV promoter is considerably weaker than the CMV promoter and typically yields >20 fold lower protein levels.

Aplicación

Cloning in a gene: This 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.

Nota de análisis

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

Información de seguridad

• Código de clase de almacenamiento: 12 - Non Combustible Liquids
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable