CROPseq-V2-Puro.P2A.mCherry
(Plasmid
#242847)
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Purpose(Empty Backbone) Backbone for cloning U6-driven sgRNAs
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Depositing Lab
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Depositing OrganizationUniversity of Texas Southwestern Medical Center
Located in the United States of America -
Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 242847 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
Backbone
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Vector backboneCROPseq-puro-v2
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Backbone manufacturerPaul Blainey, Addgene plasmid #127458
- Backbone size (bp) 10224
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Modifications to backboneP2A with mCherry fluorescent protein was inserted downstream of Puromycin resistance gene for double selection.
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Vector typeMammalian Expression, Lentiviral, CRISPR
- Promoter U6
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Selectable markersPuromycin ; mCherry
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature30°C
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Growth Strain(s)NEB Stable
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Copy numberHigh Copy
Cloning Information
- Cloning method Other
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.
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:
CROPseq-V2-Puro.P2A.mCherry was a gift from Siyuan Zhang (Addgene plasmid # 242847 ; http://n2t.net/addgene:242847 ; RRID:Addgene_242847) -
For your References section:
Tumor-intrinsic IFNγ signaling and niche adaptation drive early colonization in ovarian cancer metastasis. Aleksandrovic E, Fross SR, Golomb SM, Ma W, Liu X, Zhao Z, Das NM, Reese TC, Borges HM, Tenekeci A, Yu L, Lopez J, Zhao M, Zhong Z, Dean KM, Lea J, Xu L, Stack MS, Zhang S. Nat Commun. 2026 Sep 3;17(1):10497. doi: 10.1038/s41467-026-77222-8. 10.1038/s41467-026-77222-8 PubMed 42834039