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. : LVG00084Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00084Z |
| Description | Lentivirus particles containing luciferase reporter gene under the control of a minimal promoter and c-Myc (Myc/Max) 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-Myc/Max Luciferase Reporter Lentivirus is a powerful tool for studying c-Myc signaling pathways and transcriptional activity. These lentiviral particles contain a luciferase reporter gene driven by a minimal promoter coupled with c-Myc (Myc/Max) response elements, enabling sensitive and specific detection of c-Myc transcriptional activity. The lentiviral vector system offers several key advantages: high transduction efficiency in both dividing and non-dividing cells, stable integration into the host genome for long-term expression studies, and the ability to infect a wide range of cell types including primary cells. The reporter system provides quantitative measurement of c-Myc activity through luminescence detection, with low background noise due to the minimal promoter design.
The c-Myc/Max luciferase reporter gene lentivirus has broad applications in biomedical research. It can be used to study the regulatory mechanisms of c-Myc, a key oncogene involved in cell proliferation, apoptosis, and metabolism. Researchers can use this system to screen for compounds or genetic modifiers that affect c-Myc activity, making it valuable in drug discovery and cancer research. This reporter gene assay can be used to study the activation of the c-Myc pathway under various physiological conditions or in response to extracellular signals. Furthermore, this system can also be used to study the functional consequences of c-Myc mutations or to validate bioinformatics predictions of c-Myc target genes.
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The lentivirus exhibited high infection efficiency in our cell lines, ensuring that a majority of the cells expressed the reporter. This factor significantly enhanced the quality and accuracy of our downstream analyses.
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