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Depositing Lab
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Publication
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Sequence Information
Full plasmid sequence is not available for this item.
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 12575 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMSCV-TAP
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Backbone manufacturerSabatini Lab (Addgene Plasmid #12570)
- Backbone size w/o insert (bp) 6800
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Vector typeMammalian Expression, Retroviral
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Selectable markersPuromycin
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert namemLST8
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Alt nameGbL
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SpeciesH. sapiens (human)
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Insert Size (bp)981
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GenBank IDNP_071767
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Entrez GeneMLST8 (a.k.a. GBL, GbetaL, LST8, POP3, WAT1)
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Tag
/ Fusion Protein
- TAP (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site XhoI (destroyed during cloning)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer n/a
- 3′ sequencing primer MSCV rev primer (Common Sequencing Primers)
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
pMSCV-TAP was cut with XhoI/NotI and ligated to in-frame SalI/NotI inserts containing the sequences of mLST8.
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.
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For your Materials & Methods section:
pMSCV-TAP mLST8 (aka: GbL) was a gift from David Sabatini (Addgene plasmid # 12575 ; http://n2t.net/addgene:12575 ; RRID:Addgene_12575) -
For your References section:
mSin1 Is Necessary for Akt/PKB Phosphorylation, and Its Isoforms Define Three Distinct mTORC2s. Frias MA, Thoreen CC, Jaffe JD, Schroder W, Sculley T, Carr SA, Sabatini DM. Curr Biol. 2006 Aug 15. ():. 10.1016/j.cub.2006.08.001 PubMed 16919458
Map uploaded by the depositor.