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. : LVG00120Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00120Z |
| Description | Lentivirus particles containing firefly luciferase reporter gene under the control of EF1a 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 EF1a FLuc reporter lentivirus is a highly efficient gene delivery tool designed to stably express firefly luciferase (FLuc) under the control of the human elongation factor 1 alpha (EF1α) promoter. This lentiviral vector utilizes the powerful, constitutive EF1α promoter, ensuring long-term, high-level expression of FLuc in a variety of mammalian cell types, including dividing and non-dividing cells. The viral particles are pseudotyped with the vesicular stomatitis virus glycoprotein (VSV-G), conferring broad tropism and efficient transduction. The FLuc reporter gene integrates into the host genome, enabling sensitive and quantitative monitoring of gene expression dynamics in vitro and in vivo. Safety features such as the self-inactivating (SIN) long terminal repeat (LTR) further reduce the risk of insertional mutagenesis, making it a reliable tool for biomedical research.
The EF1a FLuc reporter lentivirus is widely used in molecular and cellular biology for a variety of applications. In gene therapy research, it is a key tool for tracking the persistence and distribution of transduced cells in animal models using bioluminescence imaging (BLI). In cancer research, the FLuc reporter gene enables non-invasive, real-time monitoring of tumor growth, metastasis, and therapeutic response. In stem cell research, this lentivirus is used to label and track the fate of transplanted stem cells, providing insights into their differentiation and engraftment efficiency. Furthermore, it is widely used in drug screening assays to assess compound efficacy by quantifying changes in FLuc activity as a surrogate marker of cellular response. The constitutive EF1α promoter ensures consistent expression across different cell types, making it ideal for comparative studies in primary cells, immortalized cell lines, and organoids.
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