-
Purpose(Empty Backbone) bacterial expression vector with Gentamycin selection, based on pBAD33
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 65098 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepBAD33
-
Backbone manufacturerBeckwith Lab
-
Modifications to backbonethe gentamicin resistance gene (aacC1) of the pUCGmlox vector was used. pUCGmlox was digested with SmaI, and the fragment containing the lox-flanked aacC1 gene was purified and cloned into the PvuII and ScaI sites in previously digested pBAD33, replacing its chloramphenicol resistance gene (cat)
-
Vector typeBacterial Expression
- Promoter pBAD
Growth in Bacteria
-
Bacterial Resistance(s)Gentamicin, 10 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Growth instructionsgrow in 10ug/ul Gentamycin. Too much gentamycin is toxic for e. coli.
-
Copy numberUnknown
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer pBad-Fwd
- 3′ sequencing primer pBad-Rev (Common Sequencing Primers)
Resource Information
-
Articles Citing this Plasmid
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
-
For your Materials & Methods section:
pBAD33-Gm was a gift from Juan Tomas (Addgene plasmid # 65098 ; http://n2t.net/addgene:65098 ; RRID:Addgene_65098) -
For your References section:
Genetics and proteomics of Aeromonas salmonicida lipopolysaccharide core biosynthesis. Jimenez N, Lacasta A, Vilches S, Reyes M, Vazquez J, Aquillini E, Merino S, Regue M, Tomas JM. J Bacteriol. 2009 Apr;191(7):2228-36. doi: 10.1128/JB.01395-08. Epub 2009 Jan 16. 10.1128/JB.01395-08 PubMed 19151135