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. : LVG00050Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00050Z |
| Description | Lentivirus particles containing second generation of anti-HER2 CAR (chimeric antigen receptor) scFv-41BB-CD3zeta. |
| Gene | ERBB2 |
| 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 | ERBB2 v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian) [ Homo sapiens ] |
| Gene Symbol | ERBB2 |
| Synonyms | NEU; NGL; HER2; TKR1; CD340; HER-2; MLN 19; HER-2/neu |
| Gene Description | v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian) |
| GeneID | 2064 |
| Uni ProtID | P04626 |
| mRNA Refseq | NM_001005862.1 |
| Protein Refseq | NP_001005862.1 |
| Chromosome Location | 17q12 |
| Function | ATP binding; ErbB-3 class receptor binding; RNA polymerase I core binding; epidermal growth factor-activated receptor activity; contributes_to growth factor binding; identical protein binding; protein C-terminus binding; protein binding; protein dimerization activity; protein heterodimerization activity; protein heterodimerization activity; protein heterodimerization activity; protein phosphatase binding; protein tyrosine kinase activity; protein tyrosine kinase activity; protein tyrosine kinase activity; receptor signaling protein tyrosine kinase activity; transmembrane receptor protein tyrosine kinase activity; transmembrane signaling receptor activity; |
| Pathway | Adaptive Immune System, organism-specific biosystem; Adherens junction, organism-specific biosystem; Adherens junction, conserved biosystem; Alpha6-Beta4 Integrin Signaling Pathway, organism-specific biosystem; Axon guidance, organism-specific biosystem; Bladder cancer, organism-specific biosystem; Bladder cancer, conserved biosystem; |
| MIM | 164870 |
scFv(HER2)-41BB-CD3ζ CAR-T Lentivirus is a gene-delivery reagent developed to generate T cells with targeted recognition of human epidermal growth factor receptor 2 (HER2/ERBB2). The encoded second-generation chimeric antigen receptor contains an extracellular anti-HER2 single-chain variable fragment (scFv), membrane-anchoring elements, the 4-1BB (CD137) costimulatory domain, and the CD3ζ activation domain. The scFv binds cell-surface HER2 independently of major histocompatibility complex presentation, while CD3ζ initiates the primary activation signal following antigen engagement. The 4-1BB domain supplies an additional costimulatory signal associated with sustained T-cell activity, survival, and persistence. Lentiviral delivery supports efficient gene transfer and stable CAR expression in transduced T cells, offering a reliable platform for producing HER2-responsive effector cells for laboratory investigation.
This lentivirus is intended for research on HER2-directed cell therapy and the functional behavior of second-generation CAR-T cells. Transduced T cells can be evaluated for CAR expression, antigen-dependent activation, cytotoxicity, cytokine secretion, proliferation, memory phenotype, and response durability. HER2-high, HER2-low, and HER2-negative target cells may be compared to investigate antigen-density thresholds, selectivity, and possible on-target effects in cells with different receptor levels. The product is applicable to experimental models of HER2-expressing breast, gastric, ovarian, lung, and other solid tumors, using appropriate in vitro assays or preclinical systems. It can also support studies of repeated antigen exposure, T-cell exhaustion, tumor-cell resistance, immune escape, and suppression within the tumor microenvironment. In comparative CAR research, this 4-1BB-containing construct provides a useful benchmark for examining how costimulatory design influences expansion, metabolism, persistence, and antitumor function relative to first-generation or CD28-based receptors. Its ready-to-use lentiviral format helps streamline exploratory screening, mechanistic studies, and early-stage evaluation of combination strategies involving checkpoint blockade, targeted agents, or other immunomodulatory approaches.
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Consistent results are crucial. Using this lentivirus, our generated CAR-T cells showed robust and reproducible anti-tumor activity in multiple HER2+ murine tumor models.
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