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. : AAV00170Z
Serotype : AAV Serotype 3 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00170Z |
| Description | AAV serotype 3 particles contain GFP under CMV promoter. |
| Serotype | AAV Serotype 3 |
| Reporter | GFP |
| 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. |
AAV is a small, 4.7 kb, linear, single-stranded DNA (ssDNA) virus in the Parvoviridae family that infects a wide range of tissue types. The AAV genome consists of two open reading frames, Cap and Rep, flanked by inverted terminal repeats (ITRs). The ITRs are the only elements of the AAV genome that must be transmitted in cis. Rep is translated to produce proteins required for AAV replication (Rep 40, 52, 68, and 78), while Cap is translated to produce the structural proteins VP1, VP2, and VP3, which form a 20- to 25-nm icosahedral capsid in a 1:1:10 ratio. Cap also produces a nonstructural protein, assembly-activating protein, which is involved in the assembly of the capsid. The ITRs allow the formation of a hairpin structure that permits primase-independent second DNA strand synthesis by the host cell DNA polymerase.
To date, 11 natural serotypes of AAV have been identified, which have different capsid structures, resulting in different tropisms. AAV tropism can be further altered by creating recombinant versions of multiple AAV serotypes, a process called pseudotyping. These pseudotyped viruses can enhance tropism for specific cell types and improve transduction efficiency in neurons.
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