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PurposeInducible Expression of SOX9
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 141404 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneFUW-tetO
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Vector typeMammalian Expression, Lentiviral
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
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Gene/Insert nameSOX9
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SpeciesH. sapiens (human)
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Entrez GeneSOX9 (a.k.a. CMD1, CMPD1, SRA1, SRXX2, SRXY10)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoR1 (destroyed during cloning)
- 3′ cloning site EcoRI (destroyed during cloning)
- 5′ sequencing primer FUW_F aactatgcgctcggg
- 3′ sequencing primer FUW_R taaagcagcgtatcc (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.
Depositor Comments
FUW-tetO-GFP (Addgene 30130) was digested with EcoRI to remove the GFP fragment and SOX9 was inserted
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:
FUW-tetO-SOX9 was a gift from Lorenz Studer (Addgene plasmid # 141404 ; http://n2t.net/addgene:141404 ; RRID:Addgene_141404) -
For your References section:
NFIA is a gliogenic switch enabling rapid derivation of functional human astrocytes from pluripotent stem cells. Tchieu J, Calder EL, Guttikonda SR, Gutzwiller EM, Aromolaran KA, Steinbeck JA, Goldstein PA, Studer L. Nat Biotechnol. 2019 Mar;37(3):267-275. doi: 10.1038/s41587-019-0035-0. Epub 2019 Feb 25. 10.1038/s41587-019-0035-0 PubMed 30804533