Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : OVT2689
| Cat. No. | OVT2689 |
| Product Type | Vector |
| Host Cell | Mammalian cells, Escherichia coli |
| Promoter | H1/TO |
| Resistance | Ampicillin |
| Selection | Puromycin |
| Vector Size | 10633 bp |
The Tet-pLKO-puro vector is a versatile and robust tool for the inducible suppression of specific genes in a variety of cellular contexts. This vector is a third-generation, HIV-1-based, lentiviral vector system specifically designed for the stable and efficient delivery of short hairpin RNA (shRNA) sequences into mammalian cells. It is an ideal tool for RNA interference (RNAi) studies as it allows controllable knockdown of desired genes without causing any permanent cellular damage or transformation.
Tet-pLKO-puro vector is designed with a bidirectional promoter system which allows the simultaneous expression of both a puromycin resistance gene and a target gene-specific shRNA. The resistant gene enables selection of transduced cells using puromycin, ensuring the efficiency and specificity of transduction. The unique feature of this vector is the Tet-On system, which enables the induction of shRNA expression by the addition of doxycycline (Dox). This system enables temporal and reversible control of gene expression, allowing the study of gene functions and effects on cellular behavior over different periods.
Tet-pLKO-puro vector is used widely in biomedical research, particularly in the field of gene expression studies. It is a lentiviral shRNA expression system that incorporates tetracycline(Tet) controlled expression mechanism.
The most significant application of this vector is in the conditional silencing of specific genes. By introducing shRNA into the genome of the target cell, scientists can turn off or 'knock down' the expression of certain genes. The Tet-pLKO-puro vector allows this silencing to be reversible. The presence of tetracycline or its derivative, doxycycline, triggers the expression of the shRNA, thereby silencing the target gene. Conversely, when the tetracycline or doxycycline is removed, the target gene’s expression is resumed.
Furthermore, researchers can utilize this vector to selectively silence genes in different stages of cellular development, tissues, or in specific disease conditions. This attribute makes the Tet-pLKO-puro vector an essential tool in studying gene functions, understanding disease mechanisms, and in the development of therapeutic strategies.
Ultimately, the Tet-pLKO-puro vector provides powerful and flexible genetic control. By manipulating the presence of tetracycline or doxycycline, researchers have an 'on-off' switch for gene expression, allowing them to investigate the role of individual genes in more detail. It also opens up potential avenues for gene therapy, where the pathological overexpression of certain genes can be 'switched off'.
A: One challenge in designing and cloning shRNAs into the vector is the large stuffer region between the cloning sites.
A: The stuffer region in the original Tet-pLKO-Puro vector is 1.9 kb.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
I appreciate the Tet-pLKO-puro vector for its potential in delivering targeted gene interference. Its use in conditional gene knockdown experiments has allowed our team to conduct our research more efficiently.
The Tet-pLKO-puro vector has been a game changer in the field of applied bioengineering. It allows regulated control over the expression of target genes, which is a huge advantage in research work.
Write a review of your use of Biogene products and services in your research. Your review can help your fellow researchers make informed purchasing decisions.