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. : LVG00121Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00121Z |
| Description | Lentivirus particles containing renilla luciferase reporter gene under the control of CMV promoter. |
| Titer | Varies lot by lot, for example, ≥1*10^7 TU/mL, ≥1*10^8 TU/mL, ≥1*10^9 TU/mL etc. |
| Size | Varies lot by lot, for example, 100 ul, 500 ul, 1 mL etc. |
| Storage | Store at -80℃. Avoid multiple freeze/thaw cycles. |
| Shipping | Frozen on dry ice |
| Summary | Creative Biogene ensures high-quality lentivirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between lentivirus particle lots. |
| Mycoplasma | Creative Biogene routinely tests for mycoplasma contamination using a mycoplasma detection kit. Cell lines are maintained for approximately 20 passages before being discarded and replaced with a new vial of early passage cells. Approximately 2 weeks after thawing, cell culture supernatants are tested for mycoplasma contamination. Creative Biogene ensures that lentiviral products are free of mycoplasma contamination. |
| Purity | Creative Biogene evaluates the level of impurities, such as residual host cell DNA or proteins, in prepared lentiviral vectors to ensure they meet quality standards. |
| Sterility | The lentiviral samples were inoculated into cell culture medium for about 5 days and the growth of bacteria and fungi was tested. Creative Biogene ensures that the lentiviral products are free of microbial contamination. |
| Transducibility | Upon requirement, Creative Biogene can perform in vitro or in vivo transduction assays to evaluate the ability of lentivirus to deliver genetic material into target cells, and assess gene expression and functional activities. |
| Proviral Identity Confirmation | All Creative Biogene lentiviral vectors are confirmed to have correctly integrated provirus using PCR. This test involves transducing cells with serial dilutions of the lentiviral vector, harvesting the cells a few days later, and isolating genomic DNA. This DNA is then used as a template to amplify a portion of the expected lentiviral insert. |
The CMV RLuc reporter lentivirus is a versatile and highly efficient lentiviral vector engineered to express the Renilla luciferase (RLuc) gene under the control of the human cytomegalovirus (CMV) immediate-early promoter. This promoter ensures robust, constitutive expression of RLuc in a variety of mammalian cell types, making it an ideal tool for gene expression studies, signal transduction analysis, and high-throughput screening. The lentiviral backbone stably integrates into the host genome, enabling long-term gene expression in both dividing and non-dividing cells. Furthermore, the virus is pseudotyped with the vesicular stomatitis virus glycoprotein (VSV-G), which broadens its tropism and improves transduction efficiency in various cell lines and primary cells. To ensure biosafety, the vector is replication-competent and incorporates essential elements, including the packaging signal (Ψ), Rev response element (RRE), and woodchuck hepatitis virus posttranscriptional regulatory element (WPRE), for optimal transgene expression.
The CMV RLuc reporter lentivirus is widely used in biomedical research to monitor gene expression dynamics, assess promoter activity, and evaluate cellular responses to stimuli. The Renilla luciferase reporter system provides a sensitive, quantitative readout, enabling researchers to track changes in gene expression in real time using bioluminescence imaging or plate-based assays. This vector is particularly valuable for studying transcriptional regulation, as the stability of the CMV promoter ensures a high signal-to-noise ratio. In drug discovery, this virus is a key tool for high-throughput screening of compounds that modulate specific pathways or promoter activity. Furthermore, its ability to transduce difficult-to-transfect cells, such as neurons or immune cells, makes it an essential component of functional genomics and in vivo studies.
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The high viral titer allowed us to use lower MOIs, minimizing cytotoxicity while maintaining strong reporter expression. Highly recommended!
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