pLenti-EML4-ALK variant 3a L1196M/G1202R
(Plasmid
#183831)
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PurposeExpress EML4-ALK fusion variant 3a (E6a;A20) harboring ALK L1196M/G1202R mutation in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 183831 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepLenti
- Backbone size w/o insert (bp) 7877
- Total vector size (bp) 10235
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Vector typeMammalian Expression, Lentiviral
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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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Copy numberUnknown
Gene/Insert 1
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Gene/Insert nameALK Receptor Tyrosine Kinase
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Alt nameALK
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SpeciesH. sapiens (human)
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Insert Size (bp)1691
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MutationL1196M/G1202R
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GenBank IDNM_004304
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Entrez GeneALK (a.k.a. ALK1, CD246, NBLST3)
- Promoter CMV
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Tag
/ Fusion Protein
- The fusion protein of EML4 exon 1-6a and ALK exon 20-29
Cloning Information for Gene/Insert 1
- Cloning method TOPO Cloning
- 5′ sequencing primer T7 (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameEMAP Like 4
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Alt nameEML4
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SpeciesH. sapiens (human)
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Insert Size (bp)667
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GenBank IDNM_019063.5
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Entrez GeneEML4 (a.k.a. C2orf2, ELP120, EMAP-4, EMAPL4, ROPP120)
- Promoter CMV
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Tag
/ Fusion Protein
- The fusion protein of EML4 exon 1-6a and ALK exon 20-29
Cloning Information for Gene/Insert 2
- Cloning method TOPO Cloning
- 5′ sequencing primer T7 (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.
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:
pLenti-EML4-ALK variant 3a L1196M/G1202R was a gift from Aaron Hata (Addgene plasmid # 183831 ; http://n2t.net/addgene:183831 ; RRID:Addgene_183831) -
For your References section:
Sequential ALK Inhibitors Can Select for Lorlatinib-Resistant Compound ALK Mutations in ALK-Positive Lung Cancer. Yoda S, Lin JJ, Lawrence MS, Burke BJ, Friboulet L, Langenbucher A, Dardaei L, Prutisto-Chang K, Dagogo-Jack I, Timofeevski S, Hubbeling H, Gainor JF, Ferris LA, Riley AK, Kattermann KE, Timonina D, Heist RS, Iafrate AJ, Benes CH, Lennerz JK, Mino-Kenudson M, Engelman JA, Johnson TW, Hata AN, Shaw AT. Cancer Discov. 2018 Jun;8(6):714-729. doi: 10.1158/2159-8290.CD-17-1256. Epub 2018 Apr 12. 10.1158/2159-8290.CD-17-1256 PubMed 29650534