pTagGFP2-H2B

pTagGFP2-H2B vector

cat.# FP196

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.


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pTagGFP2-H2BFP19620 μg€ 400 / 200*
*50% discount on the second and subsequent vectors encoding same fluorescent protein or sensor ordered by the same customer.
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Vector typemammalian expression vector
ReporterTagGFP2
Reporter codon usagemammalian
Promoter for TagGFP2PCMV IE
Host cellsmammalian
Selectionprokaryotic – kanamycin
eukaryotic – neomycin (G418)
Replicationprokaryotic – pUC ori
eukaryotic – SV40 ori
Use green fluorescent labeling of histone H2B

Vector description

pTagGFP2-H2B is a mammalian expression vector encoding TagGFP2-H2B fusion protein (see reporter description). The vector can be used for fluorescent labeling of histone H2B in living cells.

Transiently transfected HeLa cells expressing TagGFP2 fusion with human histone H2B.

TagGFP2 codon usage is optimized for high expression in mammalian cells (humanized) [Haas et al., 1996]. Human histone H2B is fused to the TagGFP2 N-terminus.

pTagGFP2-H2B vector can be used as a source of TagGFP2-H2B 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 E. coli. Therefore some restriction sites are blocked by methylation. If you wish to digest the vector using such sites you will need to transform the vector into a dam- host and make fresh DNA.

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 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 (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 E. coli. Kanr/Neor gene is linked with herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signals.


Expression in mammalian cells

pTagGFP2-H2B vector can be transfected into mammalian cells by any known transfection method. CMV promoter provides strong, constitutive expression of the TagGFP2-H2B 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

PCMV IE: 1-589
Enhancer region: 59-465
TATA box: 554-560
Transcription start point: 583
H2B-TagGFP2 fusion: 657-1769
Histone H2B protein: 657-1034
TagGFP2: 1053-1769
Stop codon: 1767-1769
SV40 early mRNA polyadenylation signal
Polyadenylation signals: 1922-1927 & 1951-1956
mRNA 3' ends: 1960 & 1972
f1 single-strand DNA origin: 2019-2474
Bacterial promoter for expression of Kanr gene
-35 region: 2536-2541
-10 region: 2559-2564
Transcription start point: 2571
SV40 origin of replication: 2815-2950
SV40 early promoter
Enhancer (72-bp tandem repeats): 2648-2719 & 2720-2791
21-bp repeats: 2795-2815, 2816-2836 & 2838-2858
Early promoter element: 2871-2877
Major transcription start points: 2867, 2905, 2911 & 2916
Kanamycin/neomycin resistance gene
Neomycin phosphotransferase coding sequences:
Start codon (ATG): 2999-3001
Stop codon: 3791-3793
G->A mutation to remove Pst I site: 3181
C->A (Arg to Ser) mutation to remove BssH II site: 3527
Herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signal
Polyadenylation signals: 4029-4034 & 4042-4047
pUC plasmid replication origin: 4378-5021


References:

  • Gorman C. High efficiency gene transfer into mammalian cells. In DNA cloning: A Practical Approach, Vol. II. Ed. D. M. Glover. (IRL Press, Oxford, U.K.). 1985; 143-90.
  • Haas J, Park EC, Seed B. Codon usage limitation in the expression of HIV-1 envelope glycoprotein. Curr Biol. 1996; 6 (3):315-24. / pmid: 8805248

Notice to Purchaser:

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.

The CMV promoter is covered under U.S. Patents 5,168,062 and 5,385,839, and its use is permitted for research purposes only. Any other use of the CMV promoter requires a license from the University of Iowa Research Foundation, 214 Technology Innovation Center, Iowa City, IA 52242.

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