JI401: Ad5 E1A/Hexon qRT-PCR standard
(Plasmid
#131753)
-
PurposePlasmid standard containing regions of the Ad5 E1A and Ad5 Hexon genes to create a qRT-PCR standard curve for detection of replication competent adenovirus (RCA).
-
Depositing Lab
-
Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 131753 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepBlueScript2SK(-)
-
Backbone manufacturerStratagene
- Backbone size w/o insert (bp) 3000
- Total vector size (bp) 3325
-
Vector typeStandard for qRT-PCR
Growth in Bacteria
-
Bacterial Resistance(s)Ampicillin, 100 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)DH5alpha
-
Copy numberHigh Copy
Gene/Insert 1
-
Gene/Insert nameAd5 E1A gene fragment
-
SpeciesAd5
-
Insert Size (bp)200
- Promoter N/A
Cloning Information for Gene/Insert 1
- Cloning method Gibson Cloning
- 5′ sequencing primer M13F (Common Sequencing Primers)
Gene/Insert 2
-
Gene/Insert nameAd5 Hexon gene fragment
-
SpeciesAd5
-
Insert Size (bp)200
- Promoter N/A
Cloning Information for Gene/Insert 2
- Cloning method Gibson Cloning
- 5′ sequencing primer M13R (Common Sequencing Primers)
Resource Information
-
Supplemental Documents
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
This plasmid is a qRT-PCR standard that enables quantification of RCA in preparations of recombinant Ad5. Please see attached protocol for more details.
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:
JI401: Ad5 E1A/Hexon qRT-PCR standard was a gift from Christopher Newgard (Addgene plasmid # 131753 ; http://n2t.net/addgene:131753 ; RRID:Addgene_131753) -
For your References section:
Creation of versatile cloning platforms for transgene expression and dCas9-based epigenome editing. Haldeman JM, Conway AE, Arlotto ME, Slentz DH, Muoio DM, Becker TC, Newgard CB. Nucleic Acids Res. 2018 Dec 27. pii: 5264291. doi: 10.1093/nar/gky1286. 10.1093/nar/gky1286 PubMed 30590691