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. : AAV00513Z
Serotype : AAV Serotype 5 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00513Z |
| Description | AAV serotype 5 particles express 2A-linked NanoLuc luciferase (NLuc) reporter and GFP reporter under the control of CAG promoter. |
| Gene | NLuc-2A-GFP |
| Serotype | AAV Serotype 5 |
| Reporter | GFP, NLuc |
| Applications |
1. Determination of optimal MOI (multiplicity of infection), administration methods etc. 2. Detection of the infection efficiency of the AAV serotype against a specific cell type or tissue. 3. Using reporter genes to visualize the distribution and expression of AAV vectors in live animals, helping assess the biodistribution and persistence of gene delivery. |
| Titer | Varies lot by lot, typically ≥1x10^12 GC/mL |
| Size | Varies lot by lot, for example, 30 μL, 100 μL, 500 μL etc. |
| Storage | Store at -80℃. Avoid multiple freeze/thaw cycles. |
| Shipping | Frozen on dry ice |
| Summary | Creative Biogene ensures high-quality AAV particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between AAV particle lots. |
| Endotoxin | Endotoxins, primarily derived from Gram-negative bacteria, can trigger adverse immune responses. Endotoxin contamination is a significant concern in the production of AAV, especially for applications in animal studies and gene therapy. Effective endotoxin quality control is essential in the development and manufacturing of AAV particles. Creative Biogene utilizes rigorous endotoxin detection methods to monitor the endotoxin level in our produced AAV particles to ensure regulatory compliance. |
| Purity | AAV purity is critical for ensuring the safety and efficacy of AAV-based applications.AAV capsids are composed of three main protein components, known as viral proteins: VP1, VP2, and VP3. These proteins play a critical role in the structure and functionality of the AAV capsid. Monitoring the VP1, VP2, and VP3 content in AAV preparations is essential for quality control in AAV production. Our AAV particles are tested for showing three clear bands of VP1, VP2 VP3 by SDS-PAGE. |
| Sterility | The AAV virus samples are inoculated into the cell culture medium for about 5 days to detect bacterial and fungal growth. |
| Transducibility | Upon requirement, Creative Biogene can perform in vitro or in vivo transduction assays to evaluate the ability of AAV to deliver genetic material into target cells or tissues, and assess gene expression and functional activities. |
| Empty vs. Full Capsids | Based-on our proprietary AAV production and purification technology, Creative Biogene can always offer AAV particles with high ratio of full capsids. If required, we can also assess the ratio for a specifc lot of AAV particles by transmission electron microscopy (TEM) or other methods. |
AAV5-CAG-NLuc-2A-GFP is a recombinant adeno-associated virus (AAV) serotype 5 vector engineered for efficient dual reporter gene expression. This vector utilizes the CAG promoter (a hybrid of the CMV enhancer and chicken β-actin promoter) to ensure robust and widespread expression in various cell types. Its unique design incorporates a 2A self-cleaving peptide, enabling co-expression of NanoLuc luciferase (NLuc) and green fluorescent protein (GFP) from the same transcript, allowing for simultaneous quantitative (luminescence) and qualitative (fluorescence) tracking of transduction efficiency. The AAV5 capsid protein enhances its tropism for central nervous system (CNS) target cells, including neurons and glial cells, while minimizing immunogenicity—a crucial feature for AAV safety. Combining high-titer production, stable long-term expression, and dual reporter genes, this vector is ideal for sensitive, long-term studies.
The applications of AAV5-CAG-NLuc-2A-GFP span basic and preclinical research. In gene therapy development, it serves as a tracer to monitor vector biodistribution and transduction kinetics through non-invasive bioluminescence imaging (BLI) and fluorescence microscopy. Researchers utilize the NLuc reporter gene, which is over 100 times brighter than firefly luciferase, to track the expression of low-abundance genes in vivo, while GFP aids in cell-type-specific validation. This vector is particularly valuable in fields such as neuroscience (e.g., mapping neural circuits), oncology (tumor model labeling), and vaccine immunology (antigen presentation studies).
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The exceptional quality of Creative Biogene's AAV5-CAG-NLuc-2A-GFP vector contributed greatly to the success of our gene therapy research. The vector delivered stable and long-lasting expression in our target cells.
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