Mut.Blimp1pGL3 (Mutant human Blimp1 promoter in pGL3-basic)
Full plasmid sequence is not available for this item.
|Item||Catalog #||Description||Quantity||Price (USD)|
|Plasmid||40341||Standard format: Plasmid sent in bacteria as agar stab||1||$65|
This material is available to academics and nonprofits only.
- Backbone size w/o insert (bp) 4818
- Total vector size (bp) 6818
Vector typeMammalian Expression, Luciferase
Growth in Bacteria
Gene/Insert nameBlimp1 promoter (mutated)
Alt namePRDM1 promoter (mutated)
SpeciesH. sapiens (human)
MutationTwo AP-1 sites at -1813 and -1647 replaced with BamHI and EcoRI restriction enzyme sites, respectively
- Promoter Blimp1
/ Fusion Protein
- Luciferase (C terminal on backbone)
- Cloning method Restriction Enzyme
- 5′ cloning site KpnI (unknown if destroyed)
- 3′ cloning site XhoI (unknown if destroyed)
- 5′ sequencing primer RVprimer3
- 3′ sequencing primer LucNrev (Common Sequencing Primers)
This mutant AP-1 site promoter, Mut.Blimp-1pGL3, was constructed by replacing the two AP-1 sites at -1813 and -1647 with BamHI and EcoRI restriction enzyme sites, respectively.
Addgene sequencing results have determined that this is a truncated promoter of ~400bp
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:Mut.Blimp1pGL3 (Mutant human Blimp1 promoter in pGL3-basic) was a gift from Alexander Dent (Addgene plasmid # 40341 ; http://n2t.net/addgene:40341 ; RRID:Addgene_40341)
For your References section:Repression of AP-1 function: a mechanism for the regulation of Blimp-1 expression and B lymphocyte differentiation by the B cell lymphoma-6 protooncogene. Vasanwala FH, Kusam S, Toney LM, Dent AL. J Immunol. 2002 Aug 15;169(4):1922-9. PubMed 12165517