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. : AAV00138Z
Serotype : AAV Serotype 1 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00138Z |
| Description | AAV serotype 1 particles contain calcium indicator GCaMP6m under CAG promoter. |
| Serotype | AAV Serotype 1 |
| 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. |
The capsids of icosahedral viruses exhibit multifunctional properties during the viral life cycle. Depending on the virus type, the functions of the capsid viral protein (VP) include receptor binding, cell entry, intracellular trafficking, genome release, capsid assembly, and genome packaging. Host immune responses may also exert additional selective pressure on the VP. Several small nonenveloped icosahedral viruses, including the single-stranded DNA (ssDNA) packaging viruses of the Parvoviridae family, have capsids that are essentially composed of a single multifunctional VP.
Adeno-associated virus (AAV) serotypes belong to the genus Dependovirus of the Parvoviridae family. They replicate efficiently in the presence of a helper virus (such as adenovirus or herpes virus) and have unique capsid-controlled tissue specificity and a tight host range. To date, 13 different human and nonhuman primate AAV serotypes have been described (AAV1 to -12 and AAV[VR-942]), and more than 100 AAV genomes across species have been identified using PCR. Based on VP sequences and antigenicity, these viruses have been divided into eight clades and clonal isolates (AAV1/AAV6, AAV2, AAV2/AAV3, AAV4, AAV5, AAV7, AAV8, and AAV9).
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The AAV1-CAG-GCaMP6m viral vector has revolutionized our calcium imaging studies. Its robust GCaMP6m expression allows us to achieve highly sensitive and rapid visualization of neuronal activity, significantly enhancing our ability to track dynamic processes in real-time.
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