-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 41187 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepACYC-Duet1 and pET21
- Backbone size w/o insert (bp) 4500
- Total vector size (bp) 6500
-
Modifications to backboneMultiple cloning site was altered to remove restriction sites. Some un-necessary parts of the vector were removed to make a compact plasmid.
-
Vector typeBacterial Expression
Growth in Bacteria
-
Bacterial Resistance(s)Chloramphenicol, 25 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameS. cerevisiae Hsp82
-
Alt nameHsp90
-
SpeciesS. cerevisiae (budding yeast)
-
Insert Size (bp)2130
- Promoter T7
-
Tag
/ Fusion Protein
- 6xHis (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NdeI (not destroyed)
- 3′ cloning site BamHI (not destroyed)
- 5′ sequencing primer T7 forward
- 3′ sequencing primer T7 reverse (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:
pACYC-T7 was a gift from Dan Bolon (Addgene plasmid # 41187 ; http://n2t.net/addgene:41187 ; RRID:Addgene_41187) -
For your References section:
Dimerization of Hsp90 is required for in vivo function. Design and analysis of monomers and dimers. Wayne N, Bolon DN. J Biol Chem. 2007 Nov 30;282(48):35386-95. Epub 2007 Oct 1. 10.1074/jbc.M703844200 PubMed 17908693