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Negative Control RLuc Reporter Lentivirus

For research use only. Not intended for any clinical use.

Cat. No. :   LVG00112Z

Storage :   -80℃ Shipping :   Frozen on dry ice

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Cat. No. LVG00112Z
Description Lentivirus particles containing renilla luciferase reporter gene under the control of a minimal promoter (TATA-box only).
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.
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The negative control RLuc reporter lentivirus is a replication-deficient, integratable lentiviral vector engineered to express Renilla luciferase under the control of a minimal TATA box promoter. This minimalist transcriptional structure produces extremely low background activity, making it an ideal negative control for luciferase-based reporter gene assays, as these assays require strict differentiation between leaky signals from upstream regulatory elements and true promoter-driven signals. Because the vector integrates into the host genome, it supports stable, long-term expression in both dividing and non-dividing cells, providing consistent baseline readings in long-term studies. The Renilla luciferase reporter gene provides a bright and well-defined signal upon addition of coelenterazine substrate, with rapid reaction kinetics and minimal spectral overlap with firefly luciferase, facilitating dual-luciferase assay design.

In practical applications, the negative control RLuc reporter lentivirus is used to establish and quantify baseline luminescence in reporter gene assays, enabling accurate background subtraction and precise signal-to-noise ratio determination. It is particularly important in experiments screening small molecules, biologics, or genetic perturbations that may affect cellular physiology or luciferase chemistry, as it helps identify auto-luminescent compounds, cytotoxic effects that alter baseline signals, or vector-related responses unrelated to promoter activity. In dual-reporter systems, the RLuc negative control can be used alongside experimental constructs to set thresholds, optimize assay parameters, and validate the linearity and dynamic range of the detection instrument.

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Customer Reviews
Perfect for Baseline Validation

Using this lentivirus as a negative control helped us rule out nonspecific signals in our experiments. The titer was accurate, and delivery was fast.

United States

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