Gateway® TurboGFP-C entry clone

cat.# FP521

The vector sequence has been compiled using the information from sequence databases, published literature, and other sources, together with partial sequences obtained by Evrogen. This vector has not been completely sequenced.

Download vector information: Data sheet (pdf) Sequence (txt) Restriction map (pdf) Restriction table (pdf)

Product Cat.# Size Price Gateway® TurboGFP-C FP521 20 μg € 320 / 160* *50% discount on the second and subsequent vectors encoding same fluorescent protein or sensor ordered by the same customer. The price does not include delivery. The price varies in different countries. Please contact your local distributor for exact prices and delivery information. Vector type Gateway® entry clone Reporter TurboGFP Reporter codon usage mammalian Promoter for TurboGFP NO Host cells prokaryotic Selection kanamycin Replication pUC ori Use Generation of fusions to the C-terminus of TurboGFP; transfer of the construct encoding TurboGFP or its fusion into Gateway® destination vectors

Multiple cloning site (MCS)

TurboGFP	Bgl II			Sac I				EcoR I			Sal I		Kpn I			Apa I*				BamH I				Stops					attL2 site
		Xho I				Hind III			Pst I*					Sac II				Sma I/Xma I
GGT.GAA.GAA.	AGA.T	CT	.C	GA.G	CT.C	AA.GCT.T	C	G.AAT.T	C	T.GCA.	G	TC.GAC	.GGT.A	CC.	GC	G.G	G	C.CC	G.	GG	A.TCC.	ACC.GGA.	TC	T.AG	G.	TAA.	C	TG.A	AC.CC...

Vector description

Gateway® TurboGFP-C entry clone is a vector containing green fluorescent protein TurboGFP gene variant with codon usage optimized for high expression in mammalian cells (humanized) [Haas et al., 1996] (see reporter description). TurboGFP coding sequence is flanked by attL1 and attL2 sites allowing easy site-specific recombination. The Invitrogen Gateway® Technology provides a rapid and highly efficient way to transfer the TurboGFP gene into a number of Gateway® destination vectors for expression in different experimental systems. Multiple cloning site (MCS) located at the 3'-end of TurboGFP gene allows to generate fusions to the TurboGFP C-terminus for expression, localization and cellular dynamics studies.

To increase mRNA translation efficiency, Kozak consensus translation initiation site is generated upstream of the TurboGFP coding sequence [Kozak, 1987].

The vector backbone contains pUC origin of replication and kanamycin resistance gene (Kan^r) for propagation and selection in E. coli.

Generation of TurboGFP fusion proteins

A localization signal or a gene of interest can be cloned into MCS of the vector both before and after site-specific recombination with a destination vector. It will be expressed as a fusion to the TurboGFP C-terminus when inserted in the same reading frame as TurboGFP and no in-frame stop codons are present.

Alternatively, TurboGFP gene can be fused to the 3'-end of a gene of interest by LR recombination of the Gateway® TurboGFP-C with a destination vector containing this gene in a correct reading frame. In this case, the protein of interest will be expressed as a fusion to the TurboGFP N-terminus.

TurboGFP-tagged fusions retain fluorescent properties of the native protein allowing fusion localization in vivo.

LR site-specific recombination

Please refer to Invitrogen Gateway® Technology description for detailed instructions regarding LR site-specific recombination reaction. In general, to transfer TurboGFP gene or TurboGFP-fusion construct into the destination vector you will need:

  - Purified plasmid DNA of Gateway® TurboGFP-C
  - A destination vector of choice
  - Invitrogen LR Clonase^TM II enzyme mix (Invitrogen Cat.# 11791-020)
  - Proteinase K solution (supplied with the LR Clonase^TM II enzyme mix)
  - TE-Buffer, pH 8.0 (10 mM Tris-HCl, pH 8.0, 1 mM EDTA)
  - Appropriate chemically competent E. coli host and growth media for expression
  - Appropriate selective plates.

Propagation in E. coli

Suitable host strains for propagation in E. coli include DH5alpha, HB101, XL1-Blue, and other general purpose strains. Plasmid incompatibility group is pMB1/ColE1. The vector confers resistance to kanamycin (30 μg/ml) to E. coli hosts. Copy number in E. coli is about 500.

Location of features

attL1 site: 14-113
Kozak translation initiation site: 129-139
TurboGFP: 136-831
MCS: 832-900
attL2 site: 908-1007
Kanamycin resistance gene: 2232-3026
pUC origin of replication: 3611-4254