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Browse > Kami Ahmad > Ahmad et al > HS-H3.3A d436-GFP
Plasmid 8697: HS-H3.3A d436-GFP
Gene/insert name: H3.3A truncated
Alternative names: H3.3^core
His3.3A
Insert size (bp): 315
Gene/insert aliases: His3.3A, H3.3, His3.3, PH3, Dmel\CG5825, CG5825
Species of gene(s): D. melanogaster (fly)
Relevant mutations/deletions: Deletion of amino acids 4-36.
Fusion proteins or tags: GFP
Terminal: C terminal on backbone
Vector backbone: na
(Search Vector Database)
Type of vector: Insect expression
Backbone size (bp): 10200
Cloning site 5': XbaI
Site destroyed during cloning: No
Cloning site 3': EagI
Site destroyed during cloning: No
5' Sequencing primer: na  (List of Sequencing Primers)
3' Sequencing primer: CCATCTAATTCAACAAGAATTGGG ACAAC
Bacteria resistance: Ampicillin
High or low copy: High Copy
Grow in standard E. coli @ 37C: Yes
Sequence:View sequence
Plasmid Provided In:DH5a
Principal Investigator:Kami Ahmad
Terms and Licenses:MTA

Comments: Same as H3.3^core. Ahmad lab #k58.

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

Click on map to enlarge

Selected features
pBR322_origin 840 - 233
ORF frame 2 1855 - 995
Ampicillin 1855 - 995
AmpR_promoter 1925 - 1897
pGEX_3_primer 2106 - 2084
5xGal4_DBD 3038 - 3131
HS_promoter 3150 - 3377
HS_promoter 3613 - 3840
GFP_R_primer 4270 - 4242
GFPfusionREV_primer 4305 - 4286
ORF frame 3 3876 - 4928
GFP(0-717) 4212 - 4928
GFP_F_primer 4865 - 4885
SV40_int 5017 - 5032
SV40_3_splice 5038 - 5085
SV40_PA_terminator 5661 - 5792
EBV_rev_primer 5749 - 5768
ORF frame 3 7149 - 7766
Unique restriction sites

FspI 1290
AatII 1990
EcoRI 3404
XhoI 3459
XbaI 3882
EagI 4197
HpaI 5657
StuI 5807
NarI 7009
SmaI 7966
EcoRV 8796

Article: The histone variant H3.3 marks active chromatin by replication-independent nucleosome assembly. Ahmad K et al. (Mol Cell 2002 Jun;9(6):1191-200. 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 8697" 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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