6his R.3-AR GUSpET28a+/pLysS
(Plasmid
#61157)
-
PurposeN-terminal His tagged round 3 aldehyde-resistant GUS expression vector
-
Depositing Labs
-
Publication
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 61157 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepET28a (+)
-
Backbone manufacturerNovagen
- Backbone size w/o insert (bp) 5369
-
Vector typeBacterial Expression
Growth in Bacteria
-
Bacterial Resistance(s)Chloramphenicol and Kanamycin, 25 & 50 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)BL21(DE3)
-
Growth instructionsContains pLysS plasmid (used for expressing low levels of T7 lysozyme). Maintain selection in kanamycin and chloramphenicol.
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameGUSAR
-
Alt nameglutaraldehyde-resistant gusA
-
Alt namebeta-glucuronidase
-
SpeciesEscherichia coli
-
MutationN66D, D151N, A219V, I396T, T480A, Q498R, D508E and K567R, compared to 6his-WT gusA-pET28a+
- Promoter T7
-
Tag
/ Fusion Protein
- 6x His (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site NcoI (not destroyed)
- 3′ cloning site HindIII (not destroyed)
- 5′ sequencing primer T7
- 3′ sequencing primer T7-term (Common Sequencing Primers)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
Matsumura lab strain number 342
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:
6his R.3-AR GUSpET28a+/pLysS was a gift from Andrew Ellington & Ichiro Matsumura (Addgene plasmid # 61157 ; http://n2t.net/addgene:61157 ; RRID:Addgene_61157) -
For your References section:
Directed evolution of the surface chemistry of the reporter enzyme beta-glucuronidase. Matsumura I, Wallingford JB, Surana NK, Vize PD, Ellington AD. Nat Biotechnol. 1999 Jul;17(7):696-701. 10.1038/10910 PubMed 10404164