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. : LV00977Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LV00977Z |
| Description | This lentivirus contains tdTOMATO under the control of human synapsin promoter. |
| Gene | tdTOMATO |
| 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 occurrence of cancer is mainly related to gene mutation, especially the activation of oncogenes, which mainly includes three activation mechanisms: gene mutation, amplification and chromosome rearrangement. At present, it is mainly treated by surgery, radiotherapy and chemotherapy. Gene therapy as a new method is in a rapid development stage, and the main approach is to introduce the target gene into the target cell. For abnormal genes in the process of tumor occurrence and development, gene fragments with therapeutic value are introduced, and they are effectively and permanently expressed in the target cells, so as to achieve the purpose of treatment. Some biological characteristics of lentiviral vectors make the idea ofgene therapy possible. Taking prostate cancer cells as the research object, Yu et al. inserted a promoter regulated by male hormones and specifically expressed in the prostate and another EGFP gene into lentivirus, and transfected normal cells and prostate cancer cells respectively. As a result, the target gene EGFP was expressed only in cancer cells, and male hormones could promote the expression of EGFP without changing the expression specificity. From the above experimental studies, it can be seen that if lentivirus is used in the clinical treatment of tumor diseases, it may bring new progress to the treatment of diseases.
Lentivirus vectors can stably transfect most non-dividing primary cells, including neurons, and can then be expressed stably and continuously, playing a therapeutic role. A large number of studies have shown that lentiviral vectors can be used to express genes related to various neurological diseases. Long-term treatment in animal models of Parkinson's disease, Alzheimer's disease, spinal cord injury and other diseases has achieved good results. Poeschla et al. constructed a lentiviral vector for transfection in rats with Parkinson's disease (PD). The results showed that it can improve the number of rotations of rats, protect and prevent the degeneration of dopamine neurons, and alleviate the neurological symptoms of PD.
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Ordered multiple batches over the last year for different projects. The consistently high titer ensures reliable and reproducible transduction across experiments and animal cohorts.
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