pTagFP635-H2B vector

cat.# FP386

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 pTagFP635-H2B FP386 20 μg € 400.00 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 TagFP635 Reporter codon usage mammalian Promoter for TagFP635 PCMV IE Host cells mammalian Selection prokaryotic - kanamycin eukaryotic - neomycin (G418) Replication prokaryotic - pUC ori eukaryotic - SV40 ori Use far-red fluorescent labeling of histone H2B

Vector description

pTagFP635-H2B is a mammalian expression vector encoding TagFP635-H2B fusion protein (see TagFP635 description). The vector can be used for fluorescent labeling of histone H2B in living cells.

TagFP635 codon usage is optimized for high expression in mammalian cells, i.e. humanized (Haas et al., 1996). Human histone H2B is fused to the TagFP635 N-terminus.

pTagFP635-H2B can be used as a source of TagFP635-H2B hybrid sequence. The vector backbone contains unique restriction sites that permit it excision and further insertion into expression vector of choice.

The vector backbone also 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

pTagFP635-H2B can be transfected into mammalian cells by any known transfection method. CMV promoter provides strong, constitutive expression of the TagFP635-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

P_{CMV IE}: 1-589
Enhancer region: 59-465
TATA box: 554-560
Transcription start point: 583
Histone H2B: 657-1034
TagFP635: 1053-1766
SV40 early mRNA polyadenylation signal
Polyadenylation signals: 1919-1924 & 1948-1953
mRNA 3' ends: 1957 & 1969
f1 single-strand DNA origin: 2016-2471
Bacterial promoter for expression of Kan^r gene
-35 region: 2533-2538
-10 region: 2556-2561
Transcription start point: 2568
SV40 origin of replication: 2812-2947
SV40 early promoter
Enhancer (72-bp tandem repeats): 2645-2716 & 2717-2788
21-bp repeats: 2792-2812, 2813-2833 & 2835-2855
Early promoter element: 2868-2874
Major transcription start points: 2864, 2902, 2908 & 2913
Kanamycin/neomycin resistance gene
Neomycin phosphotransferase coding sequences:
Start codon (ATG): 2996-2998
Stop codon: 3788-3790
G->A mutation to remove Pst I site: 3178
C->A (Arg to Ser) mutation to remove BssH II site: 3524
Herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signal
Polyadenylation signals: 4026-4031 & 4039-4044
pUC plasmid replication origin: 4375-5018