pYSG-IBA105 vector

IBA Lifescience Kontakt z doradcą
Yeast expression vector encoding an N-terminal Twin-Strep-tag®
pYSG-IBA105 vector

The pYSG-IBA105 vector is designed for high-level expression of target proteins with an N-terminal Twin-Strep-tag® in yeast. The vector carries an ampicillin resistance cassette for selection of transformed E. coli cells, the ColE1 origin for a high plasmid copy number, the copper-inducible promoter (CUP1) for controlled high-level expression, the URA3 auxotrophy marker for selection after transformation (do not use URA3 for selection during expression), the LEU2d auxotrophy marker for selection to increase plasmid copy number for expression (do not use LEU2d for selection after transformation), and the 2 micron ori for episomal replication in yeast. Please note that cloning into pYSG-IBA Acceptor Vectors compulsorily requires the restriction enzyme Esp3I since no other MCS for the integration of a gene of interest is available. In addition to the direct cloning of the gene of interest into pYSG-IBA vectors with Esp3I, another option via a so-called Entry Vector is possible.

Specifications

  • Affinity Tag N'-terminal: Twin-Strep-tag®
  • Cloning Method: Direct cloning using restriction enzyme Esp3I
  • Concentration: 250 ng/µl
  • Expression Host: Yeast
  • Form: Suspension in TE buffer
  • Possible Application: Vector for recombinant expression in yeast
  • Promoter: CUP1 Promoter
  • Resistance: Ampicillin
  • Sequence: See Documents
  • Size: 7913 bp

Podobne produkty

pLSG-IBA162 vector

pLSG-IBA162 vector

IBA Lifescience
Więcej
pESG-IBA142 vector

pESG-IBA142 vector

IBA Lifescience
Więcej
pCSG-IBA3 vector

pCSG-IBA3 vector

IBA Lifescience
Więcej