pShuttle-FEN1mWT
(Plasmid
#35032)
-
Depositing Lab
-
Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
---|---|---|---|---|---|
Plasmid | 35032 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
-
Vector backbonepShuttle
-
Backbone manufacturerStratgene
- Backbone size w/o insert (bp) 7500
- Total vector size (bp) 9000
-
Vector typeMammalian Expression, Adenoviral
Growth in Bacteria
-
Bacterial Resistance(s)Kanamycin, 50 μg/mL
-
Growth Temperature37°C
-
Growth Strain(s)XL10 Gold
-
Copy numberHigh Copy
Gene/Insert
-
Gene/Insert nameFEN1mWT
-
SpeciesM. musculus (mouse)
-
Insert Size (bp)1500
- Promoter CMV
-
Tag
/ Fusion Protein
- Flag (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRV (destroyed during cloning)
- 3′ cloning site EcoRV (destroyed during cloning)
- 5′ sequencing primer GGTctatataagcagagctg
- 3′ sequencing primer CTGatcataatcagccataccac (Common Sequencing Primers)
Resource Information
-
A portion of this plasmid was derived from a plasmid made byBINGHUI SHEN -- CITY OF HOPE
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:
pShuttle-FEN1mWT was a gift from Sheila Stewart (Addgene plasmid # 35032 ; http://n2t.net/addgene:35032 ; RRID:Addgene_35032) -
For your References section:
FEN1 ensures telomere stability by facilitating replication fork re-initiation. Saharia A, Teasley DC, Duxin JP, Dao B, Chiappinelli KB, Stewart SA. J Biol Chem. 2010 Aug 27;285(35):27057-66. Epub 2010 Jun 15. 10.1074/jbc.M110.112276 PubMed 20551483