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Invitrogen™ pcDNA™4/TO Mammalian Expression Vector

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Quantity:
20 μg
Description
- Uses repressor mechanism that blocks transcription from the powerful CMV promoter in absence of tetracycline
- Because the T-REx System elements do not use viral transactivators, user can achieve high-level expression from complete CMV promoter without secondary, nonspecific activation of host genes
- Two tetracycline operator sequences (TetO2) have been inserted between TATA box of the CMV promoter and the transcriptional start site: The TetO2 sequence itself has no effect on expression When tetracycline repressor protein (TR) is present, it effectively binds TetO2 sites and blocks transcription initiation
- Tetracycline added to culture medium binds to, and changes conformation of, TR protein
- This change causes TR protein to release TetO2 sites, derepressing transcription from the CMV promoter for high-level expression of gene of interest
- Expression levels can be modulated based on tetracycline concentration and can be induced to levels that are achieved with constitutive CMV expression vectors
- Zeocin or hygromycin resistance gene for effective selection of stable mammalian cell lines
- Large multiple cloning site to simplify cloning
Mammalian Expression, Protein Expression, Proteins, Expression, Isolation and Analysis, Regulated Expression, Targeted Integration

Specifications
Specifications
Constitutive or Inducible System | Inducible |
Delivery Type | Transfection |
Inducing Agent | Tetracycline |
Promoter | CMV/TO |
Product Type | Mammalian Expression Vector |
Selection Agent (Eukaryotic) | Zeocin™ |
Protein Tag | Untagged |
Cloning Method | Restriction Enzyme/MCS |
Quantity | 20 μg |
Vector | pcDNA |
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For Research Use Only. Not for use in diagnostic procedures.
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