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Browse > Jon Ashwell > Li et al > pcdna3.1 hciap2
Plasmid 8338: pcdna3.1 hciap2
Gene/insert name: cIAP2
Insert size (bp): 1800
Gene/insert aliases: BIRC3, AIP1, API2, MIHC, CIAP2, HAIP1, HIAP1, MALT2, RNF49, c-IAP2
Species of gene(s): H. sapiens (human)
Fusion proteins or tags: myc
Terminal: N terminal on backbone
Vector backbone: pcDNA3.1
(Search Vector Database)
Backbone manufacturer: Invitrogen
Type of vector: Mammalian expression,Luciferase
Backbone size (bp): 5400
Cloning site 5': Xho1
Site destroyed during cloning: No
Cloning site 3': BamH1
Site destroyed during cloning: No
5' Sequencing primer: T7  (List of Sequencing Primers)
3' Sequencing primer: SP6
Bacteria resistance: Ampicillin
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:Jon Ashwell
Terms and Licenses:MTA, Luciferase LULL

Comments: There is a N100D change in the amino acid sequence, according to the author this mutation does not affect protein function.

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

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Article: TNF-RII and c-IAP1 mediate ubiquitination and degradation of TRAF2. Li X et al. (Nature 2002 Mar 21;416(6878):345-7. 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 8338" 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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