CCT8-GST
(Plasmid
#245887)
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PurposeExpress human CCT8 tagged with GST in bacteria
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Depositing Lab
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Depositing OrganizationTurku Bioscience Centre
Located in Finland -
Publication
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 245887 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
Backbone
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Vector backbonepGEX 4T1
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Vector typeBacterial 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 numberUnknown
Gene/Insert
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Gene/Insert nameCCT8
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SpeciesH. sapiens (human)
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Entrez GeneCCT8 (a.k.a. C21orf112, Cctq, D21S246, PRED71)
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Tag
/ Fusion Protein
- GST (N terminal on backbone)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SmaI (unknown if destroyed)
- 3′ cloning site XhoI (unknown if destroyed)
- 5′ sequencing primer gst
- (Common Sequencing Primers)
Resource Information
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
The CCT8-GST construct was generated by cloning the CCT8 sequence from the CCT8-pcDNA3.1(+)-N-eGFP plasmid into the pGEX 4T1 vector. The GFP-CCT8 insert was obtained by KpnI digestion, blunted, then cut with XhoI and ligated into the SmaI/XhoI-digested pGEX 4T1 backbone. Please visit https://doi.org/10.64898/2025.12.03.691809 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:
CCT8-GST was a gift from Guillaume Jacquemet (Addgene plasmid # 245887 ; http://n2t.net/addgene:245887 ; RRID:Addgene_245887) -
For your References section:
CCT8 associates with the MYO10 motor domain and regulates filopodia and breast cancer cell invasion. Popović A, Ojalill M, Touma C, Ball NJ, Miihkinen M, Joshi O, Dibus M, Pylvänäinen J, Ivaska J, Goult BT, Jacquemet G. J Cell Sci jcs.265278 10.1242/jcs.265278