pBABE-LynG
(Plasmid
#206867)
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PurposeExpression of LynG probe - LynAnchor-eGFP
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 206867 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBABE-puro (Plasmid #1764)
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Backbone manufactureraddgene
- Backbone size w/o insert (bp) 5086
- Total vector size (bp) 5954
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Modifications to backboneLynG insert
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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)NEB Stable
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Growth instructionsThis plasmid has been stored as a glycerol stock in NEB stable cells to reduce recombination, however the Herten Lab uses DH5alpha without issue.
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameLynG
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Alt nameLynAnchor-eGFP
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SpeciesM. musculus (mouse); Aequorea victoria
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Insert Size (bp)774
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MutationContains Lyn amino acids 1-16
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GenBank IDNM_001111096.2 AAB02572.1
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Tag
/ Fusion Protein
- eGFP (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site PacI (not destroyed)
- 5′ sequencing primer -
- 3′ sequencing primer - (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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.
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:
pBABE-LynG was a gift from Dirk-Peter Herten (Addgene plasmid # 206867 ; http://n2t.net/addgene:206867 ; RRID:Addgene_206867) -
For your References section:
ProDOL - A General Method to Accurately Count Molecular Complexes and Determine the Degree of Labelling in Cells Using Protein Tags. Tashev SA, Euchner J, Yserentant K, Hänselmann S, Hild F, Chmielewicz W, Hummert J, Schwörer F, Tsopoulidis N, Germer S, Saßmannshausen Z, Fackler OT, Klingmüller U, Herten D. Nat Methods (2024) 10.1038/s41592-024-02376-6