mSECFP/pcDNA3
(Plasmid
#51951)
-
Purposemammalian expression of mSECFP, a monomeric super enhanced cyan fluorescent protein
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 51951 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepcDNA3
-
Backbone manufacturerInvitrogen
-
Vector typeMammalian Expression
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert namemSECFP
-
SpeciesSynthetic
-
Insert Size (bp)700
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer CMV-F
- 3′ sequencing primer BGHrev (Common Sequencing Primers)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
GenBank accession number: AB435576. ECFP was modified to improve its brightness and oligomeric property by substituting Serine at 72 for Alanine, Serine at 175 for Glysine, and Alanine at 206 for Lysine, yielding mseCFP.
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:
mSECFP/pcDNA3 was a gift from Takeharu Nagai (Addgene plasmid # 51951 ; http://n2t.net/addgene:51951 ; RRID:Addgene_51951) -
For your References section:
Direct measurement of protein dynamics inside cells using a rationally designed photoconvertible protein. Matsuda T, Miyawaki A, Nagai T. Nat Methods. 2008 Apr;5(4):339-45. doi: 10.1038/nmeth.1193. Epub 2008 Mar 16. 10.1038/nmeth.1193 PubMed 18345008