pTO-sp-NLuc_FRT (control) plasmid

Contributors

Inventor Institute
Andrii Domanskyi, Tina Sket University of Helsinki
SKU: 161757
Product description: Endoplasmic reticulum (ER) stress is caused by the accumulation of unfolded proteins in the ER, which leads to the activation of unfolded protein response (UPR) through three transmembrane protein sensors located in the ER membrane. The sensors correspond to three branches of the UPR, namely protein kinase RNA-like endoplasmic reticulum kinase (PERK), activating transcription factor 6 (ATF6), and inositol-requiring enzyme 1 (IRE1) branches. Upon ER stress, IRE1 dimerizes and oligomerizes, and its endonuclease domain is activated. It specifically targets X-box-binding protein 1 (XBP1) mRNA, from which a 26 nt intron is spliced. This allows a complete translation of spliced XBP1 mRNA into a functional protein that acts as a transcription factor. Together with the other pathways, the UPR leads to a decrease in the protein folding load by causing a reduction in the general level of protein translation, and by inducing the expression of protein folding machinery. However, if the UPR is activated continuously for a long time, the apoptotic pathway will be triggered, and the cell will die. ER stress and UPR are associated with various disorders, such as some types of cancer, diabetes, chronic inflammatory syndromes, and particularly neurodegeneration. For example, in Parkinson’s disease, it was suggested that prolonged ER stress induces the extensive apoptosis of dopaminergic neurons in substantia nigra pars compacta region of the midbrain. The control pTO-sp-NLuc_FRT XBP1 splicing reporter assay plasmid does not contain the XBP1 intron fragment in NanoLuc luciferase gene, and thus cell transfected with this plasmid will express NanoLuc luciferase irrespectively of XBP1 splicing.
Alternate name: pTO-sp-NLuc_FRT (control) XBP1 splicing reporter assay (XSARA) control plasmid, XSARA control plasmid
Cat. #: 161757
Research Fields: Cell biology
Application: Control plasmid for XBP1 reporter assay. Upon induction with doxycycline, HEK293-NLuc control cells will express NLuc protein irrespectively of XBP1 splicing, providing a control for XSARA assay. The plasmid can also be used for transient transfection.
Backbone size without insert: 5061 bp
Bacterial resistance: Ampicillin
Selectable markers: Hygromycin
Application: Control plasmid for XBP1 reporter assay. Upon induction with doxycycline, HEK293-NLuc control cells will express NLuc protein irrespectively of XBP1 splicing, providing a control for XSARA assay. The plasmid can also be used for transient transfection.
Shipping conditions: +4° C or dry ice
Plasmid amplification details: Stbl3 E.coli
Plasmid copy number: High copy number

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