Purpose / Description: (Empty Backbone) FX cloning E.coli expression vector with araBAD promoter and N-terminal 1x His tag and 3C protease cleavage site
Reference: A versatile and efficient high-throughput cloning tool for structural biology.
Bacteria Resistance: Chloramphenicol and Bleocin (Zeocin)
Vector backbone: pPICZ
Vector type: Yeast Expression
Total vector size: 5778 bp
Backbone Manufacturer: Invitrogen
Modification to backbone: modified for compatibility with FX cloning and added tags/fusion proteins
Copy number: Low
Growth strain: DB3.1
Growth temperature: 37°C
Antibiotics Resistance: Unknown
Depositor comment: Constructed by Dr. Stephan Schenck, Dutzler lab, Dept of Biochemistry, University of Zurich, Switzerland.
Gene / Insert: None
Cloning method: Unknown
Selectable marker: Zeocin
Promoter: AOX1
Tag / fusion protein: 3C protease site (PreScission site) (C terminal on backbone); GFP (C terminal on backbone); decaHIS (1x His) (C terminal on backbone)