BB1_23_MS2bind_VP64_SV40NLS
(Plasmid
#161479)
-
PurposeBB1 encoding a MS2 binding VP64 fusion protein with an additional SV40 NLS
-
Depositing Labs
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 161479 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backboneBB1_L_23_syn_BsaI
- Backbone size w/o insert (bp) 2000
- Total vector size (bp) 2529
-
Vector typeSynthetic Biology
Growth in Bacteria
-
Bacterial Resistance(s)Kanamycin, 50 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameMS2 binding protein + VP64 activation domain
-
Alt nameMS2 - VP64
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BpiI (destroyed during cloning)
- 3′ cloning site BpiI (destroyed during cloning)
- 5′ sequencing primer CAGGAAACAGCTATGAC
- 3′ sequencing primer GTAAAACGACGGCCAGTT (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:
BB1_23_MS2bind_VP64_SV40NLS was a gift from Brigitte Gasser & Diethard Mattanovich (Addgene plasmid # 161479 ; http://n2t.net/addgene:161479 ; RRID:Addgene_161479) -
For your References section:
Fine-Tuning of Transcription in Pichia pastoris Using dCas9 and RNA Scaffolds. Baumschabl M, Prielhofer R, Mattanovich D, Steiger MG. ACS Synth Biol. 2020 Dec 18;9(12):3202-3209. doi: 10.1021/acssynbio.0c00214. Epub 2020 Nov 12. 10.1021/acssynbio.0c00214 PubMed 33180466