pTagRFP-laminB1 vector

cat.# FP370

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 pTagRFP-laminB1 FP370 20 μg € 400 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 mammalian expression vector Reporter TagRFP Reporter codon usage mammalian Promoter for TagRFP PCMV IE Host cells mammalian Selection prokaryotic – kanamycin eukaryotic – neomycin (G418) Replication prokaryotic – pUC ori eukaryotic – SV40 ori Use red (orange) fluorescent labeling of lamin B1

Vector description

pTagRFP-laminB1 is a mammalian expression vector encoding TagRFP-lamin B1 fusion protein (see reporter description). The vector can be used for fluorescent labeling of lamin B1 in living cells.

Transiently transfected HeLa cells expressing TagRFP fusion with lamin B1. Image was kindly provided by Michael W. Davidson (Florida State University).

TagRFP codon usage is optimized for high expression in mammalian cells (humanized) [Haas et al., 1996]. Human lamin B1 is fused to the TagRFP C-terminus. To increase mRNA translation efficiency, Kozak consensus translation initiation site is generated upstream of the TagRFP-lamin B1 coding sequence [Kozak, 1987].

pTagRFP-laminB1 vector can be used as a source of TagRFP-lamin B1 hybrid sequence. The vector backbone contains unique restriction sites that permit its excision and further insertion into expression vector of choice.

The vector backbone contains immediate early promoter of cytomegalovirus (P_{CMV IE}) for protein expression, SV40 origin for replication in mammalian cells expressing SV40 T-antigen, pUC origin of replication for propagation in E. coli, and f1 origin for single-stranded DNA production. SV40 polyadenylation signals (SV40 poly A) direct proper processing of the 3'-end of the reporter mRNA.

SV40 early promoter (P_SV40) provides neomycin resistance gene (Neo^r) expression to select stably transfected eukaryotic cells using G418. Bacterial promoter (P) provides kanamycin resistance gene expression (Kan^r) in E. coli. Kan^r/Neo^r gene is linked with herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signals.

Expression in mammalian cells

pTagRFP-laminB1 vector can be transfected into mammalian cells by any known transfection method. CMV promoter provides strong, constitutive expression of the TagRFP-lamin B1 fusion in eukaryotic cells. If required, stable transformants can be selected using G418 [Gorman, 1985].

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

P_{CMV IE}: 1-589
Enhancer region: 59-465
TATA box: 554-560
Transcription start point: 583
Kozak consensus translation initiation site: 606-616
TagRFP
Start codon (ATG): 613-615
Last amino acid in TagRFP: 1321-1323
Lamin B1: 1354-3114
Stop codon: 3112-3114
SV40 early mRNA polyadenylation signal
Polyadenylation signals: 3275-3280 & 3304-3309
mRNA 3' ends: 3313 & 3325
f1 single-strand DNA origin: 3372-3827
Bacterial promoter for expression of Kan^r gene
-35 region: 3889-3894
-10 region: 3912-3917
Transcription start point: 3924
SV40 origin of replication: 4168-4303
SV40 early promoter
Enhancer (72-bp tandem repeats): 4001-4072 & 4073-4144
21-bp repeats: 4148-4168, 4169-4189 & 4191-4211
Early promoter element: 4224-4230
Major transcription start points: 4220, 4258, 4264 & 4269
Kanamycin/neomycin resistance gene
Neomycin phosphotransferase coding sequences:
Start codon (ATG): 4352-4354
Stop codon: 5144-5146
G->A mutation to remove Pst I site: 4534
C->A (Arg to Ser) mutation to remove BssH II site: 4880
Herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signal
Polyadenylation signals: 5382-5387 & 5395-5400
pUC plasmid replication origin: 5731-6374