pHIE822 pCMV Bglobin intron VSVGmut K47Q R354A in pMD2
(Plasmid
#252774)
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PurposeVSV-G mutant with abolished receptor binding, but maintained fusogenic capacity
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Depositing Lab
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 252774 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $89 | |
Backbone
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Vector backbonepMD2
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Vector typeMammalian Expression
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 nameVSVG K47Q R354A
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SpeciesSynthetic
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MutationK47Q, R354A
- Promoter CMV
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer N/A
- 3′ sequencing primer N/A
- (Common Sequencing Primers)
Resource Information
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
Leonard Lab plasmid reference number: L4435 . Please visit https://doi.org/10.1101/2025.07.02.662894 for bioRxiv preprint.
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:
pHIE822 pCMV Bglobin intron VSVGmut K47Q R354A in pMD2 was a gift from Joshua Leonard (Addgene plasmid # 252774 ; http://n2t.net/addgene:252774 ; RRID:Addgene_252774) -
For your References section:
Distinguishing Pseudotransduction and True Transduction Enables Characterization and Bioengineering of Extracellular Vesicle-Adeno-Associated Virus Vectors. Boucher JD, Stranford DM, Edelstein HI, Tullman-Ercek D, Kamat NP, Leonard JN. J Extracell Vesicles. 2026 Apr;15(4):e70258. doi: 10.1002/jev2.70258. 10.1002/jev2.70258 PubMed 41942279