missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Thermo Scientific™ pCRE Tluc16-DD Vector for Luciferase Assays
Insert promoter sequences for genes of interest into Thermo Scientific™ Tluc16 Vectors to measure gene regulation using the intracellular TurboLuc™ 16 (Tluc16) luciferase reporter in luciferase assays.
Brand: Thermo Scientific™ 88247
This item is not returnable.
View return policy
Description
The Thermo Scientific pMCS Tluc16 Vectors are multiple cloning site (MCS) vectors designed to accept a promoter sequence for study of gene regulation using the intracellular TurboLuc™16 (Tluc16) luciferase reporter.
- Intracellular Tluc16 luciferase gene, optimized for high expression in mammalian systems
- Multiple cloning sites provide versatility for transfer of regulatory elements from one vector to another
- Synthetic polyA terminator and Transcriptional Pause Site (TPS) included upstream of MCS to minimize non-specific transcriptional read-through
- Dual-destabilization (DD) technology reduces accumulation of Tluc16 luciferase mRNA and protein in cells, enhancing the responsiveness of the assay
- Optimized minimal core promoter (minP) and 5' UTR region for efficient expression of Tluc16 luciferase
- Hygromycin resistance gene for use as selection marker to generate mammalian stable cell lines
- Prepared pNF-κB, and pCRE Tluc16-DD Vectors are designed to monitor the activation of NFκB protein and cAMP-binding protein (CREB) in mammalian cells
- Prepared pEF1α variety includes a modified version of the Elongated Factor 1α (EF1α) promoter for constitutive Tluc16 luciferase expression in mammalian cells
Specifications
Transcriptional Reporter Vector | |
Transfection | |
Store in freezer (-5 to -30°C). | |
minP-CRE |
Restriction Enzyme ⁄ MCS | |
10 μg | |
Reporter Assays |
Product Content Correction
Your input is important to us. Please complete this form to provide feedback related to the content on this product.
Product Title
For Research Use Only. Not for use in diagnostic procedures.
Spot an opportunity for improvement?Share a Content Correction