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. : LVG00086Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00086Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and CCAAT-Enhancer Binding Protein (C/EBP) response element. |
| 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 C/EBP luciferase reporter lentiviral vector is an advanced research tool that places a luciferase reporter gene under the control of a minimal promoter and a CCAAT enhancer-binding protein (C/EBP) response element. This lentiviral vector system offers several key advantages for gene regulation studies. First, lentiviral delivery ensures stable integration of the reporter gene into the host genome, enabling long-term expression in both dividing and non-dividing cells. The system exhibits high transduction efficiency in a variety of cell types, including primary cells that are typically difficult to transfect. The minimal promoter design reduces background noise while maintaining sensitivity to C/EBP transcriptional activity. The inclusion of the C/EBP response element allows researchers to specifically monitor the activity of this important transcription factor family.
This powerful reporter system has broad applications in studying C/EBP-mediated transcriptional regulation and related biological processes. Researchers primarily utilize it to investigate the activation status and functional roles of C/EBP family members (α, β, δ, etc.) in various physiological and pathological contexts, including adipogenesis, hematopoiesis, liver regeneration, and inflammatory responses. Luciferase readings allow for quantitative measurement of C/EBP activity via sensitive luminescence detection, facilitating high-throughput screening of compounds or genes that modulate C/EBP signaling pathways. In disease research, this tool helps elucidate the role of C/EBP in metabolic disorders, cancer, and immune diseases by enabling temporal monitoring of pathway activation in relevant cell models. The lentiviral vector format makes it particularly valuable for establishing stable reporter cell lines, which can be used for long-term studies of C/EBP dynamics during differentiation processes or drug interventions.
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The luciferase reporter system provides remarkably clear signals, making it easier to quantify results. This clarity significantly improved the accuracy of my data analysis.
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