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. : LVG00027Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00027Z |
| Description | Lentivirus particles containing second generation of anti-CEA CAR (chimeric antigen receptor) scFv-CD28-CD3zeta. |
| Gene | CEACAM5 |
| 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. |
| Gene Name | CEACAM5 carcinoembryonic antigen-related cell adhesion molecule 5 [ Homo sapiens ] |
| Gene Symbol | CEACAM5 |
| Synonyms | CEACAM5; carcinoembryonic antigen-related cell adhesion molecule 5; CEA; CD66e; meconium antigen 100; DKFZp781M2392; |
| Gene ID | 1048 |
| Uni Prot ID | P06731 |
| m RNA Refseq | BC034671 |
| Chromosome Location | 19q13.1-q13.2 |
| MIM | 114890 |
The scFv(CEA)-CD28-CD3zeta CAR-T lentivirus is a second-generation replication-deficient lentiviral vector designed to deliver a chimeric antigen receptor that combines precise CEA recognition with robust and controllable T cell activation. This vector incorporates a high-affinity anti-CEA single-chain variable fragment for selective target binding, paired with a rationally designed hinge/transmembrane region and an intracellular CD28 co-stimulatory domain fused to the CD3zeta signaling module. This structure supports durable surface expression and robust downstream signaling upon antigen binding, promoting rapid T cell activation, proliferation, and cytokine production while maintaining functional persistence. The vector utilizes a self-inactivating backbone and a separate packaging system to enhance biosafety and reduce the risk of insertional activation, and is designed for stable genomic integration, thus maintaining transgene expression during cell expansion.
This lentiviral vector is ideally suited for preclinical studies focused on CEA-positive solid tumors, including colorectal cancer, gastric cancer, pancreatic cancer, and certain lung adenocarcinomas. It enables the rapid generation of CEA-targeted CAR-T cells for in vitro evaluation of cytotoxicity, cytokine release, degranulation, activation kinetics, and exhaustion markers, as well as for co-culture studies investigating tumor-immune interactions. In vivo, it supports proof-of-concept efficacy studies in xenograft or patient-derived models, facilitating the assessment of tumor control, CAR-T cell persistence, and biodistribution. The vector is also valuable in safety risk assessment processes, including on-target/off-target tumor assessment and sensitivity assessment to varying antigen densities, thus informing target selection and clinical translation strategies.
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Used this product in mouse xenograft models—clear tumor regression observed with minimal off-target effects. The CEA-specific CAR design is well optimized for therapeutic efficacy.
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