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The new DNAVAC research project targets the removal of antibiotics in veterinary DNA-vaccines
The new DNAVAC research project targets the removal of antibiotics in veterinary
Delphi Genetics participation to the AMERE study granted by the European Space Agency (ESA)
Nivelles, Belgium, 23rd of January 2012 – Lambda-X, Delphi Genetics, The d
Delphi Genetics at Peptalk 2012
Delphi Genetics will be present at the Peptalk meeting taking place in San
Delphi Genetics announces that all the bacterial strains present in its research kits are completely
Yokohama, Japan, 16 of December 2011 - Delphi Genetics announced today during a
You are here : Products > Protein Expression
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The StabyExpress T7 kit contains all the necessary elements for cloning of a gene-of-interest and its expression in Escherichia coli. The kit combines two technologies (T7 expression and Staby plasmid stabilization) that allow high-yield protein expression and standardization of the production-protocol. Vectors with His-tag and/or GST-tag are available. Additional CYS21 and SE1 competent bacteria can be purchased separately. |
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The StabyCodon T7 kit combines three technologies to ensure high-yield and standardized expression of eukaryote proteins in Escherichia coli. These technologies are (i) T7-controled expression, (ii) plasmid stabilization, and (iii) |
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The CherryTMExpress kit allows direct visualization (by eye!) of your protein of interest during protein production in E. coli and protein purification. No special requirements or reagents are needed. It is also |
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The CherryTMCodon kit allows direct visualization (by eye!) of your protein of interest during protein production in E. coli and protein purification. Special requirements or reagents are not needed. It is also possible to quantify the protein concentration at any step by spectral measurement. The CherryTMCodon kit combines multiple advantages: protein |
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The StabyTMSubCloning kit was designed to transfer your genes of interest from StabyCloning vector (pSTC1) to efficient expression vectors. This transfer is very easy and powerful: using simple restriction sites and ligation, your insert is oriented and selected in the appropriate sub-cloning vector, it is not required to purify your insert.The multiple cloning sites of destination vectors contain the same compatible restriction sites. Consequently, one restriction of the pSCT1 vector is compatible with all StabySubCloning vectors. |
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