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. : AAV00236Z
Serotype : AAV serotype DJ/8 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00236Z |
| Description | AAV serotype DJ/8 particles contain Cre recombinase under CMV promoter and GFP under independent CMV promoter. |
| Serotype | AAV serotype DJ/8 |
| 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. |
Adeno-associated viruses (AAV) are derived from defective parvoviruses that rely on essential helper functions provided by other viruses, such as adenoviruses and herpesviruses, for efficient viral replication and spread. AAV has no etiological association with any known disease and has been successfully used to establish efficient and long-term gene expression in vivo in a variety of tissues without significant cellular immune responses or toxicity.
AAV has a single-stranded DNA genome consisting of approximately 4.7 kb. All identified AAV serotypes share three key features, including two AAV terminal repeats (ITRs), a rep region, and a cap region. The ITRs are capable of forming T-shaped secondary structures and are the only cis-elements required for AAV replication, packaging, integration, and rescue. The rep region encodes four overlapping proteins, designated Rep78, Rep68, Rep52, and Rep40 based on the apparent molecular weight of the proteins. In addition to their well-defined role in AAV replication, the Rep proteins regulate AAV packaging and site-specific integration. The cap region encodes three structural proteins, VP1, VP2, and VP3. These three proteins share the same reading frame.
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I have used the AAV DJ/8-Cre-GFP vector for several experiments, and it consistently provides exceptional efficiency in gene delivery. The transduction rates are impressive, and the expression of GFP is strong and consistent across different cell types.
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