-
PurposeExpresses ATG8 fused at the N terminus to GFP under the control of the endogenous promoter in the pRS414 vector.
-
Depositing Lab
-
Publication
-
Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 49424 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepRS414
- Backbone size w/o insert (bp) 4788
-
Vector typeBacterial Expression, Yeast Expression
-
Selectable markersTRP1
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberLow Copy
Gene/Insert
-
Gene/Insert nameautophagy-related 8
-
Alt nameATG8
-
Alt nameAUT7
-
Alt nameAPG8
-
SpeciesS. cerevisiae (budding yeast)
-
Entrez GeneATG8 (a.k.a. YBL078C, APG8, AUT7, CVT5)
- Promoter ATG8
-
Tag
/ Fusion Protein
- GFP (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site XhoI (not destroyed)
- 5′ sequencing primer NA
- 3′ sequencing primer NA (Common Sequencing Primers)
Resource Information
-
Article Citing this Plasmid
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
-
For your Materials & Methods section:
GFP-ATG8(414)/GFP-AUT7(414) was a gift from Daniel Klionsky (Addgene plasmid # 49424 ; http://n2t.net/addgene:49424 ; RRID:Addgene_49424) -
For your References section:
Chemical genetic analysis of Apg1 reveals a non-kinase role in the induction of autophagy. Abeliovich H, Zhang C, Dunn WA Jr, Shokat KM, Klionsky DJ. Mol Biol Cell. 2003 Feb;14(2):477-90. 10.1091/mbc.e02-07-0413 PubMed 12589048