hnRNPA1_allW_D262V-FLAG-IRES-eGFP
(Plasmid
#234621)
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PurposeMammalian expression of full-length hnRNPA1 D262V with all aromatic amino acids in the C-terminal LCD mutated to W keeping the hexapeptide fibril core (SYNDFG) and the PY-NLS intact.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 234621 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepcDNA4/TO/myc-His A
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Backbone manufacturerThermo Fisher Scientific
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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 namehnRNPA1 allW D262V
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SpeciesH. sapiens (human)
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MutationFamillial ALS mutation D262V, all aromatic amino acids in C-terminal domain (186-320) mutated to W, except for two Y-s in the hexapeptide fibril core (SYNVFG) and PY-NLS
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Entrez GeneHNRNPA1 (a.k.a. ALS19, ALS20, HNRPA1, HNRPA1L3, IBMPFD3, MPD3, UP 1, hnRNP A1, hnRNP-A1)
- Promoter CMV
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Tag
/ Fusion Protein
- FLAG (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Unknown (unknown if destroyed)
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
Please visit https://doi.org/10.1101/2024.02.28.582569 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:
hnRNPA1_allW_D262V-FLAG-IRES-eGFP was a gift from Tanja Mittag (Addgene plasmid # 234621 ; http://n2t.net/addgene:234621 ; RRID:Addgene_234621) -
For your References section:
Metastable condensates suppress conversion to amyloid fibrils. Das T, Zaidi F, Farag M, Ruff KM, Messing J, Taylor JP, Pappu RV, Mittag T. bioRxiv [Preprint]. 2024 Mar 3:2024.02.28.582569. doi: 10.1101/2024.02.28.582569. 10.1101/2024.02.28.582569 PubMed 38464104