pJTRSF50
(Plasmid
#89700)
-
PurposeFor production of GFP with "GLP" N-tag and "TRNCL" for C-tag for cyclisation control.
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 89700 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepRSF-1b
-
Backbone manufacturerNovagen
- Backbone size w/o insert (bp) 3669
-
Modifications to backboneNcoI to NdeI mutation
-
Vector typeBacterial Expression
Growth in Bacteria
-
Bacterial Resistance(s)Kanamycin, 50 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameSMT3_GLP_H6_GFP_TRNCL
-
Insert Size (bp)1038
- Promoter T7
-
Tag
/ Fusion Protein
- SMT3 (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NdeI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer T7 term (Common Sequencing Primers)
Resource Information
-
Supplemental Documents
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:
pJTRSF50 was a gift from Hideo Iwai (Addgene plasmid # 89700 ; http://n2t.net/addgene:89700 ; RRID:Addgene_89700) -
For your References section:
Segmental isotopic labeling of a single-domain globular protein without any refolding step by an asparaginyl endopeptidase. Mikula KM, Tascon I, Tommila JJ, Iwai H. FEBS Lett. 2017 Mar 30. doi: 10.1002/1873-3468.12640. 10.1002/1873-3468.12640 PubMed 28369872