pHAGE2-Ef1a-SOX17E57D-3xFLAG
(Plasmid
#216199)
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PurposeOverexpress human SOX17E57D in HEK 293T cells for use in whole cell extract EMSAs
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 216199 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepHAGE2-EF1a
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Vector typeLentiviral
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 nameSOX17
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SpeciesH. sapiens (human)
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MutationGlu113Glu (silent mutation); Glu120Glu (silent mutation); Glu122Asp
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Entrez GeneSOX17 (a.k.a. VUR3)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site Unknown (unknown if destroyed)
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.
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:
pHAGE2-Ef1a-SOX17E57D-3xFLAG was a gift from Ralf Jauch (Addgene plasmid # 216199 ; http://n2t.net/addgene:216199 ; RRID:Addgene_216199) -
For your References section:
An acidic residue within the OCT4 dimerization interface of SOX17 is necessary and sufficient to overcome its pluripotency-inducing activity. Ho SY, Hu H, Ho DHH, Renom APS, Yeung SW, Boerner F, Weng M, Hutchins AP, Jauch R. Stem Cell Reports. 2025 Mar 11;20(3):102398. doi: 10.1016/j.stemcr.2025.102398. Epub 2025 Feb 6. 10.1016/j.stemcr.2025.102398 PubMed 39919754