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. : LVG00018Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00018Z |
| Description | Lentivirus particles containing third generation of anti-CD33 CAR (chimeric antigen receptor) scFv-CD28-OX40-CD3zeta. |
| Gene | CD33 |
| 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 | CD33 CD33 molecule [ Homo sapiens ] |
| Gene Symbol | CD33 |
| Synonyms | p67; SIGLEC3; SIGLEC-3 |
| Gene Description | CD33 molecule |
| Gene ID | 945 |
| Uni Prot ID | C9JEN7 |
| m RNA Refseq | NM_001082618.1 |
| Protein Refseq | NP_001076087.1 |
| Chromosome Location | 19q13.3 |
| Function | carbohydrate binding; receptor activity; |
| Pathway | Hematopoietic cell lineage, organism-specific biosystem; Hematopoietic cell lineage, conserved biosystem; |
| MIM | 159590 |
Chimeric antigen receptor T-cell (CAR-T) therapy is a groundbreaking immunotherapy that harnesses the power of a patient''s own T cells to target and destroy cancer cells. This innovative treatment begins with T cells collected from the patient''s blood. These cells are then genetically modified in the laboratory to express a chimeric antigen receptor (CAR), designed to recognize a specific antigen on the surface of tumor cells. Once the T cells are modified, they are expanded and infused back into the patient. The CAR enables these modified T cells to recognize and bind to cancer cells, ultimately activating the T cells and triggering an immune response that significantly shrinks or eliminates the tumor. CAR-T therapy has achieved remarkable success in treating certain hematological malignancies, such as acute lymphoblastic leukemia (ALL) and certain types of lymphoma, offering hope for patients who have exhausted other treatment options.
CAR-T lentivirus, as a vector for genetically modifying T cells, has played a crucial role in the development of CAR-T therapy. Derived from lentivirus, lentiviral vectors, due to their unique integration ability, can integrate into the host cell genome, enabling sustained expression of the CAR, and are used to deliver the CAR gene to T cells. This is particularly important for long-term efficacy because it enables the modified T cells to maintain their ability to target cancer. The use of lentivirus not only enhances the persistence of CAR expression, but also promotes the potential for the simultaneous construction of multiple CARs or other therapeutic genes. The process involves transducing a lentiviral vector containing the CAR gene into human T cells to ensure that the T cells can effectively recognize and attack tumor cells. Studies have shown that CAR-T cells derived from lentiviral modified T cells can exhibit a strong anti-tumor response, making this approach a key component in the development of personalized cancer therapies.
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The CD33-specific scFv exhibits strong binding to myeloid leukemia cells in our assays. Minimal off-target effects—exactly as described!
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