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Browse > Geoff Wahl > Kanda et al > H2B-GFP
Plasmid 11680: H2B-GFP
Gene/insert name: Human histone H2B
Insert size (bp): 380
GenBank/Entrez ID of insert: X00088
Gene/insert aliases: HIST1H2BJ, H2B/r, H2BFR
Species of gene(s): H. sapiens (human)
Fusion proteins or tags: EGFP
Terminal: C terminal on backbone
Vector backbone: pEGFP-N1  (Search Vector Database)
Type of vector: Mammalian expression
Backbone size (bp): 4733
Cloning site 5': KpnI
Site destroyed during cloning: No
Cloning site 3': BamHI
Site destroyed during cloning: No
5' Sequencing primer: None  (List of Sequencing Primers)
3' Sequencing primer: EGFP-N
Bacteria resistance: Kanamycin
High or low copy: High Copy
Grow in standard E. coli @ 37C: Yes
Selectable markers: Neomycin
Sequence:View sequence
Plasmid Provided In:DH5a
Principal Investigator:Geoff Wahl
Terms and Licenses:MTA

Addgene has sequenced a portion of this plasmid for verification. Click here for the sequencing result.

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Selected features
CAG_enhancer 65 - 352
CMV_immearly_promoter 10 - 562
CMV_fwd_primer 519 - 539
CMV_promoter 520 - 589
EGFP_N_primer 1119 - 1098
Orf frame 3 657 - 1772
EGFP 1053 - 1769
EGFP_C_primer 1706 - 1727
EBV_rev_primer 1986 - 2005
f1_origin 2461 - 2155
AmpR_promoter 2540 - 2568
pBABE_3_primer 2654 - 2634
SV40_enhancer 2855 - 2640
SV40_promoter 2652 - 2920
SV40_origin 2819 - 2896
SV40pro_F_primer 2881 - 2900
Orf frame 3 3003 - 3797
Neomycin 3006 - 3794
TK_PA_terminator 3972 - 4241
pBR322_origin 4389 - 5008
Unique restriction sites

AseI 7
NdeI 234
NheI 591
BglII 609
XhoI 613
SacI 620
HindIII 622
PstI 638
SalI 639
KpnI 649
BamHI 1034
AgeI 1040
NotI 1775
XbaI 1785
HpaI 1894
AflII 2013
StuI 2952
ClaI 2971
NarI 3131
FspI 3233
ApaLI 4735

Article: Histone-GFP fusion protein enables sensitive analysis of chromosome dynamics in living mammalian cells. Kanda T et al. (Curr Biol. 1998 Mar 26. 8(7):377-85. Pubmed)

Please acknowledge the principal investigator and cite this article if you use this plasmid in a publication.

Also, please include the text "Addgene plasmid 11680" in your Materials and Methods section. This information allows Addgene to create a link from the plasmid page to your publication.

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