-
Purpose(Empty Backbone) Empty backbone for Agrobacterium tumefaciens-mediated transformation of Fusarium oxysporum
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 104175 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepCAMBIA1300
-
Backbone manufacturerCAMBIA, Canberra, Australia
- Backbone size (bp) 8960
-
Modifications to backbonepCAMBIA1300 was digested with with XhoI and BstXIA to remove the hph gene under control of the Cauliflower mosaic virus 35S (CaMV35S). The ends were blunted and ligated to a 1.4-kb HpaI fragment of pCB1004 containing the hph gene under the Aspergillus nidulans trpC promoter. The 3′ end of the hph gene was then ligated to the CaMV35S poly (A) termination signal.
-
Vector typeFungal expression
- Promoter none
-
Selectable markersHygromycin
Growth in Bacteria
-
Bacterial Resistance(s)Kanamycin, 50 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberUnknown
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer unknown (Common Sequencing Primers)
Resource Information
-
A portion of this plasmid was derived from a plasmid made bypCB1004: Carroll, A. M., Sweigard, J. A., and Valent, B. 1994. Improved vectors for selecting resistance to hygromycin. Fungal Genet. Newsl. 41:22.
-
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:
pBHt2 was a gift from Seogchan Kang (Addgene plasmid # 104175 ; http://n2t.net/addgene:104175 ; RRID:Addgene_104175) -
For your References section:
Agrobacterium-Mediated Transformation of Fusarium oxysporum: An Efficient Tool for Insertional Mutagenesis and Gene Transfer. Mullins ED, Chen X, Romaine P, Raina R, Geiser DM, Kang S. Phytopathology. 2001 Feb;91(2):173-80. doi: 10.1094/PHYTO.2001.91.2.173. 10.1094/PHYTO.2001.91.2.173 PubMed 18944391