pTXG-hTDG
(Plasmid
#52281)
-
PurposeBacterial expression of human TDG C-terminally fused to GyrA intein and GST
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 52281 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepTXB3
-
Backbone manufacturerNew England Biolabs
- Backbone size w/o insert (bp) 7194
- Total vector size (bp) 8394
-
Modifications to backboneCBD domain (StuI-BamHI fragment) replaced by GST (StuI-BglII fragment)
-
Vector typeBacterial Expression
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Growth instructionsIn combination with a second vector for protein expression in BL21(DE3) cells, the selection pressure was reduced by half to 50 mg/L Ampicillin
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert namehTDG
-
Alt namethymine DNA glycosylase
-
SpeciesH. sapiens (human)
-
Insert Size (bp)1232
-
GenBank IDNM_003211.4
-
Entrez GeneTDG (a.k.a. hTDG)
- Promoter T7
-
Tag
/ Fusion Protein
- GyrA-intein-GST (C terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NcoI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer TAATACGACTCACTATAGGG (Common Sequencing Primers)
Resource Information
-
A portion of this plasmid was derived from a plasmid made by
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:
pTXG-hTDG was a gift from Primo Schaer (Addgene plasmid # 52281 ; http://n2t.net/addgene:52281 ; RRID:Addgene_52281) -
For your References section:
Versatile Recombinant SUMOylation System for the Production of SUMO-Modified Protein. Weber AR, Schuermann D, Schar P. PLoS One. 2014 Jul 9;9(7):e102157. doi: 10.1371/journal.pone.0102157. eCollection 2014. 10.1371/journal.pone.0102157 PubMed 25007328