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. : LVG00053Z
Storage : -80℃ Shipping : Frozen on dry ice
Titer: Size:
| Cat. No. | LVG00053Z |
| Description | Lentivirus particles containing third generation of anti-HER2 CAR (chimeric antigen receptor) scFv-CD28-41BB-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)-CD28-41BB-CD3ζ CAR-T Lentivirus is a gene-delivery reagent designed to generate T cells with targeted recognition of human epidermal growth factor receptor 2 (HER2/ERBB2). The encoded third-generation chimeric antigen receptor contains an extracellular anti-HER2 single-chain variable fragment (scFv), membrane-anchoring elements, tandem intracellular costimulatory domains from CD28 and 4-1BB (CD137), and the CD3ζ activation domain. The scFv recognizes HER2 on the cell surface independently of major histocompatibility complex presentation. Upon antigen binding, CD3ζ initiates T-cell activation, while CD28 and 4-1BB provide complementary costimulatory signals associated with effector activity, proliferation, survival, and persistence. Lentiviral delivery supports efficient gene transfer and stable CAR expression in transduced T cells, offering a practical platform for investigating how dual costimulation shapes HER2-directed immune responses.
This product is intended for research on HER2-targeted cellular immunotherapy and the functional evaluation of third-generation CAR-T cells. Transduced cells can be studied for CAR expression, antigen-dependent activation, cytotoxicity, cytokine secretion, expansion, survival, memory differentiation, and exhaustion. Comparisons using HER2-high, HER2-low, and HER2-negative target cells can help define antigen-density requirements, selectivity, and possible on-target effects across different expression levels. The resulting CAR-T cells are suitable for appropriately designed studies involving HER2-expressing breast, gastric, ovarian, lung, and other solid-tumor models. The construct also provides a useful benchmark for comparing dual-costimulatory signaling with first-generation CD3ζ-only receptors or second-generation CARs containing either CD28 or 4-1BB. Additional applications include examining repeated antigen exposure, tumor-cell resistance, immune escape, and CAR-T-cell performance within suppressive tumor microenvironments. Its lentiviral format helps streamline exploratory screening, mechanistic studies, and early-stage assessment of combination approaches involving checkpoint inhibitors, targeted agents, cytokines, or other immune-modulating strategies.
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The consistency in titer, transduction efficiency, and resulting CAR-T cell function (cytokine release, cytotoxicity assays) across batches was outstanding. This reliability is essential for generating publishable data.
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