Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : AAV00534Z
Serotype : AAV Serotype 9 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00534Z |
| Description | AAV serotype 9 particles express no insert gene under the control of human synapsin promoter (hSyn) for control use. |
| Gene | NULL |
| Serotype | AAV Serotype 9 |
| 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. |
AAV9-hSyn-NULL is an adeno-associated virus serotype 9 (AAV9) vector engineered to serve as a crucial experimental control in neuroscience research. This viral vector construct combines several advantages: the AAV9 serotype exhibits superior neuronal tropism and efficient blood-brain barrier penetration compared to other AAV serotypes; while the human synapsin (hSyn) promoter provides neuron-specific expression. The "NULL" in the name indicates that the vector contains no transgene insert, making it particularly important for controlling non-specific effects of viral transduction. The strong activity of the hSyn promoter in neurons, combined with the high transduction efficiency of AAV9, provides an ideal platform for comparison with experimental vectors containing therapeutic or reporter genes.
In experimental applications, AAV9-hSyn-NULL plays a key role in both in vitro and in vivo neuroscience research. Researchers commonly use this control vector to establish baseline measurements for viral transduction efficiency, neuronal toxicity assessment, and characterization of immune responses in animal models. It is particularly important in optogenetics, chemogenetics, and gene therapy studies, where control groups must account for the potential effects of the viral capsid or promoter activity. The vector facilitates experimental design involving stereotaxic injections into brain regions such as the hippocampus or striatum by controlling for volume effects and surgical variables. Drug development utilizes AAV9-hSyn-NULL for preclinical safety assessments of gene therapies targeting neurological disorders. The combination of neuron-specific targeting and empty vector insertion makes AAV9-hSyn-NULL an indispensable tool in rigorous neuroscience research and therapeutic development.
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