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.
pTagGFP2-laminB1 is a mammalian expression vector encoding TagGFP2-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 TagGFP2 fusion with human lamin B1.
TagGFP2 codon usage is optimized for high expression in mammalian cells (humanized) [Haas et al., 1996]. Human lamin B1 is fused to the TagGFP2 C-terminus. To increase mRNA translation efficiency, Kozak consensus translation initiation site is generated upstream of the TagGFP2-lamin B1 coding sequence [Kozak, 1987].
pTagGFP2-laminB1 vector can be used as a source of TagGFP2-lamin B1 hybrid sequence. The vector backbone contains unique restriction sites that permit its excision and further insertion into expression vector of choice.
Note: The plasmid DNA was isolated from dam+-methylated
The vector backbone contains immediate early promoter of cytomegalovirus (PCMV IE) for protein expression, SV40 origin for replication in mammalian cells expressing SV40 T-antigen, pUC origin of replication for propagation in
SV40 early promoter (PSV40) provides neomycin resistance gene (Neor) expression to select stably transfected eukaryotic cells using G418. Bacterial promoter (P) provides kanamycin resistance gene expression (Kanr) in
Expression in mammalian cells
pTagGFP2-laminB1 vector can be transfected into mammalian cells by any known transfection method. CMV promoter provides strong, constitutive expression of the TagGFP2-lamin B1 fusion in eukaryotic cells. If required, stable transformants can be selected using G418 [Gorman, 1985].
Suitable host strains for propagation in
Location of features
PCMV IE: 1-589
Enhancer region: 59-465
TATA box: 554-560
Transcription start point: 583
Kozak consensus translation initiation site: 600-610
TagGFP2-laminB1 fusion: 607-3111
Start codon (ATG): 607-609
Last amino acid in TagGFP2: 1318-1320
Lamin B1: 1351-3111
Stop codon: 3109-3111
SV40 early mRNA polyadenylation signal
Polyadenylation signals: 3272-3277 & 3301-3306
mRNA 3' ends: 3310 & 3322
f1 single-strand DNA origin: 3369-3824
Bacterial promoter for expression of Kanr gene
-35 region: 3886-3891
-10 region: 3909-3914
Transcription start point: 3921
SV40 origin of replication: 4165-4300
SV40 early promoter
Enhancer (72-bp tandem repeats): 3998-4069 & 4070-4141
21-bp repeats: 4145-4165, 4166-4186 & 4188-4208
Early promoter element: 4221-4227
Major transcription start points: 4217, 4255, 4261 & 4266
Kanamycin/neomycin resistance gene
Neomycin phosphotransferase coding sequences:
Start codon (ATG): 4349-4351
Stop codon: 5141-5143
G->A mutation to remove Pst I site: 4531
C->A (Arg to Ser) mutation to remove BssH II site: 4877
Herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signal
Polyadenylation signals: 5379-5384 & 5392-5397
pUC plasmid replication origin: 5728-6371
TagGFP2-related materials (also referred to as "Products") are intended for research use only. The Products are covered by U.S. Pat. 7,417,131; 7,605,230; 7,888,113; European Pat. 06809023; and other Evrogen Patents and/or Patent applications pending. By use of these Products, you accept the terms and conditions of the applicable Limited Use Label License.
Copyright 2002-2019 Evrogen. All rights reserved.
Evrogen JSC, 16/10 Miklukho-Maklaya str., Moscow, Russia, Tel +7(495)988-4084, Fax +7(495)988-4085, e-mail:email@example.com