pIZ/V5-His Vector Kit
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Invitrogen™

pIZ/V5-His Vector Kit

El kit InsectSelect™ incluye el vector pIZ/V5-His para la expresión de alto nivel en una variedad de células de insectos.Más información
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Número de catálogoCantidad
V800001
también denominado V8000-01
1 kit
Número de catálogo V800001
también denominado V8000-01
Precio (MXN)
-
Cantidad:
1 kit
El kit InsectSelect™ incluye el vector pIZ/V5-His para la expresión de alto nivel en una variedad de células de insectos. Este vector excepcionalmente pequeño tiene varias características que facilitan la expresión, el análisis y la detección de proteínas recombinantes en células de insectos:

• El promotor OpIE2 de la expresión constitutiva
• El gen de resistencia al Zeocin™ para la selección rápida de líneas celulares transfectadas de forma estable
• Secuencia de epítopo C-terminal V5 y polihistidina (6xHis) para la detección con anticuerpo anti-V5 de Invitrogen y purificación rápida mediante resina quelante de níquel
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Tipo de productoVector de expresión de células de insectos
Posición de la etiqueta de la proteína (a su gen)C-terminal
Cantidad1 kit
VectorpIZ
Método de clonaciónEnzimas de restricción/MCS
Línea de productosInsectSelect
PromotorOplE2
Etiqueta de proteínaEtiqueta His (6x), Etiqueta de epítopo V5
Unit Size1 kit
Contenido y almacenamiento
El kit InsectSelect™ incluye 20 μg cada uno de pIZT/V5-His y pIZT/V5-His/CAT superenrollados y liofilizados, 2 μg de cebadores de secuenciación inversa OpIE2 liofilizados,1 g de Zeocin™, reactivo Cellfectin™ y 1 L de medio para la línea de células de insectos elegida. Las células Sf9 se suministran con medios para insectos GIBCO™ Grace, mientras que las células High Five™ se suministran con medio sin suero GIBCO™ Express Five™. El kit de vectores pIZ/V5-His contiene únicamente los vectores de expresión y el cebador según lo descrito anteriormente. Almacene las células de insectos congeladas en nitrógeno líquido. Conserve el medio y el reactivo Cellfectin™ a +4°C. Conservar todos los demás reactivos a -20°C. Se garantiza la estabilidad de todos los reactivos durante 6 meses si se almacenan correctamente.

Preguntas frecuentes

Do I need to include a Kozak sequence for expression of recombinant proteins in insect cells?

While the importance of a Kozak consensus sequence in translation initiation has been demonstrated in mammalian cells, there seems to be some debate as to whether the Kozak rules are as stringent in insect cells. The only way to determine its importance would be a direct comparison of expression of the same protein from different initiation sequences. Even then, the rules for optimal expression of one protein may not hold for another. Here are two references which indicate that a Kozak consensus sequence does not have any effect on efficiency of expression in insect cells:

- Hills D, Crane-Robinson C (1995) Baculovirus expression of human basic fibroblast growth factor from a synthetic gene: role of the Kozak consensus and comparison with bacterial expression.
- Biochim Biophys Acta 1260(1):14-20.
- Ranjan A, Hasnain SE (1995) Influence of codon usage and translational initiation codon context in the AcNPV-based expression system: computer analysis using homologous and heterologous genes. Virus Genes 9(2):149-153.

Do I need to include a ribosomal binding site (RBS/Shine Dalgarno sequence) or Kozak sequence when I clone my gene of interest?

ATG is often sufficient for efficient translation initiation although it depends upon the gene of interest. The best advice is to keep the native start site found in the cDNA unless one knows that it is not functionally ideal. If concerned about expression, it is advisable to test two constructs, one with the native start site and the other with a Shine Dalgarno sequence/RBS or consensus Kozak sequence (ACCAUGG), as the case may be. In general, all expression vectors that have an N-terminal fusion will already have a RBS or initiation site for translation.

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

Can you tell me the difference between a Shine-Dalgarno sequence and a Kozak sequence?

Prokaryotic mRNAs contain a Shine-Dalgarno sequence, also known as a ribosome binding site (RBS), which is composed of the polypurine sequence AGGAGG located just 5’ of the AUG initiation codon. This sequence allows the message to bind efficiently to the ribosome due to its complementarity with the 3’-end of the 16S rRNA. Similarly, eukaryotic (and specifically mammalian) mRNA also contains sequence information important for efficient translation. However, this sequence, termed a Kozak sequence, is not a true ribosome binding site, but rather a translation initiation enhancer. The Kozak consensus sequence is ACCAUGG, where AUG is the initiation codon. A purine (A/G) in position -3 has a dominant effect; with a pyrimidine (C/T) in position -3, translation becomes more sensitive to changes in positions -1, -2, and +4. Expression levels can be reduced up to 95% when the -3 position is changed from a purine to pyrimidine. The +4 position has less influence on expression levels where approximately 50% reduction is seen. See the following references:

- Kozak, M. (1986) Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes. Cell 44, 283-292.
- Kozak, M. (1987) At least six nucleotides preceding the AUG initiator codon enhance translation in mammalian cells. J. Mol. Biol. 196, 947-950.
- Kozak, M. (1987) An analysis of 5´-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 15, 8125-8148.
- Kozak, M. (1989) The scanning model for translation: An update. J. Cell Biol. 108, 229-241.
- Kozak, M. (1990) Evaluation of the fidelity of initiation of translation in reticulocyte lysates from commercial sources. Nucleic Acids Res. 18, 2828.

Note: The optimal Kozak sequence for Drosophila differs slightly, and yeast do not follow this rule at all. See the following references:

- Romanos, M.A., Scorer, C.A., Clare, J.J. (1992) Foreign gene expression in yeast: a review. Yeast 8, 423-488.
- Cavaneer, D.R. (1987) Comparison of the consensus sequence flanking translational start sites in Drosophila and vertebrates. Nucleic Acids Res. 15, 1353-1361.

Find additional tips, troubleshooting help, and resources within our Protein Expression Support Center.

Citations & References (1)

Citations & References
Abstract
Proteolysis of CCN1 by plasmin: functional implications.
Authors:Pendurthi UR,Tran TT,Post M,Rao LV
Journal:Cancer research
PubMed ID:16266990
Plasmin is shown to play a crucial role in many pathophysiological processes, primarily through its ability to degrade extracellular matrix and/or mobilizing growth factors that are sequestered in the extracellular matrix. CCN1 is a matricellular protein whose expression is upregulated in cancer and various vascular diseases. The present study was ... More