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. : RV00003Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | RV00003Z |
| Description | Premade MMLV-based, VSV-G pseudotyped retroviral particles that contain mCherry reporter gene. |
| Gene | mCherry |
| Titer | Varies lot by lot, for example, ≥1*10^7 TU/mL or ≥1*10^8 TU/mL. |
| 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 retrovirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between retrovirus 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 retrovirus products are free of mycoplasma contamination. |
| Purity | Creative Biogene evaluates the level of impurities, such as residual host cell DNA or proteins, in prepared retrovirus vectors to ensure they meet quality standards. |
| Sterility | The retrovirus 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 retrovirus 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 retrovirus to deliver genetic material into target cells, and assess gene expression and functional activities. |
| Proviral Identity Confirmation | All Creative Biogene retrovirus vectors are confirmed to have correctly integrated provirus using PCR. This test involves transducing cells with serial dilutions of the retrovirus 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 retrovirus insert. |
The mCherry MMLV Retrovirus is a replication-deficient vector system derived from the Moloney Murine Leukemia Virus, engineered to facilitate the stable delivery and expression of the mCherry red fluorescent protein in mammalian cells. As a member of the gammaretrovirus family, its defining characteristic is a dependence on host cell mitosis for successful integration; the viral pre-integration complex requires the breakdown of the nuclear envelope during cell division to access the host genome. The vector typically utilizes a strong viral LTR or internal promoter to drive the expression of mCherry, a monomeric fluorophore prized for its rapid maturation time and high photostability. Unlike transient expression systems, this retroviral platform ensures that the mCherry transgene is covalently integrated into the host DNA, resulting in constitutive and heritable fluorescence that persists throughout the lifetime of the cell and its progeny.
In laboratory research, the mCherry MMLV Retrovirus is a primary tool for the generation of stable reporter cell lines and the execution of long-term lineage tracing studies. Because the red fluorescence is passed to all daughter cells, it is frequently employed in developmental biology and oncology to monitor cell fate, migration, and clonal expansion over extended periods. The distinct spectral properties of mCherry make it an ideal candidate for multiplexing with GFP or other blue-light excited proteins, allowing for the simultaneous tracking of multiple cellular components without significant signal overlap. Furthermore, its proliferation-dependent integration mechanism is often exploited to specifically label and isolate actively dividing cells within heterogeneous populations, such as identifying neurogenic cells in specific niches or tracking activated immune cells during an inflammatory response. This makes the vector particularly valuable for studies where distinguishing between quiescent and proliferative states is essential for the experimental outcome.
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The mCherry MMLV Retrovirus gave us robust, red fluorescence across multiple cell types. The viral prep was clean, and transduction was efficient—ideal for tracking cell lineages.
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