pAAV-U6-AlbEx14-mNG
(Plasmid
#201780)
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Purposeknocks in mNeonGreen into exon 14 of Alb to produce Alb-mNeonGreen fusion protein in mice
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 201780 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
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Backbone
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Vector backbonepAAV.GFAP.Cre.WPRE.hGH
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Backbone manufacturerAddgene plasmid #105550
- Backbone size w/o insert (bp) 2876
- Total vector size (bp) 7454
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Vector typeAAV, CRISPR
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 numberHigh Copy
Gene/Insert 1
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Gene/Insert nameAlb gRNA
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SpeciesM. musculus (mouse)
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Insert Size (bp)3226
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Entrez GeneAlb (a.k.a. Alb-1, Alb1, BCL002)
- Promoter U6
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site NotI (not destroyed)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer n/a (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameAlb_LHA-mNeonGreen-Alb_RHA
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SpeciesM. musculus (mouse)
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Entrez GeneAlb (a.k.a. Alb-1, Alb1, BCL002)
Cloning Information for Gene/Insert 2
- Cloning method Restriction Enzyme
- 5′ cloning site NotI (not destroyed)
- 3′ cloning site NotI (not destroyed)
- 5′ sequencing primer n/a (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.
Depositor Comments
Please visit https://www.biorxiv.org/content/10.1101/2023.07.10.548084v1 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:
pAAV-U6-AlbEx14-mNG was a gift from Hajime Hirase (Addgene plasmid # 201780 ; http://n2t.net/addgene:201780 ; RRID:Addgene_201780) -
For your References section:
Virally induced CRISPR/Cas9-based knock-in of fluorescent albumin allows long-term visualization of cerebral circulation in infant and adult mice. Vittani M, Knak PAG, Fukuda M, Nagao M, Wang X, Kjaerby C, Konno A, Hirai H, Nedergaard M, Hirase H. Fluorescence Imaging of the Brain. Neuromethods, vol 209. Humana, New York, NY. 10.1007/978-1-0716-4011-1_6