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. : AAV00547Z
Serotype : AAV Serotype AAV-BI30 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00547Z |
| Description | AAV serotype BI30 particles express GFP reporter gene under the control of CAG promoter for CNS endothelial cell specific expression. |
| Gene | GFP |
| Serotype | AAV Serotype AAV-BI30 |
| 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. |
| Target Gene | GFP |
Adeno-associated viruses (AAV) are small viruses that infect humans and other primates. They are nonenveloped viruses belonging to the genus Dependoparvovirus of the family Parvoviridae. This small virus (20 nm) was first identified in 1965 as a contaminant of adenovirus (Ad) preparations. Several natural AAV serotypes are known, of which AAV2 is the most typical and commonly used. These serotypes differ in their capsid structure, resulting in different tropisms and immunogenicity in host organisms.
Briefly, the AAV capsid is an icosahedral virion with a diameter of 25 nm and 60 viral protein (VP) subunits (triangulation number, T = 1) (6, 10). The protein coat is composed of three VP subunits (VP1, VP2, and VP3) in a ratio of 1:1:10, each of which has a conserved jelly-roll fold or beta barrel structure with interlaced loops connecting the beta strands. Single-particle cryo-electron microscopy (cryo-EM) has been used to map the receptor and antigen footprints of different AAV serotypes. Receptor usage by different AAV serotypes has been well studied, particularly with regard to the cell surface glycans used for attachment and, more recently, the essential cellular receptor KIAA0319L or AAVR. Structural models of the trimeric AAV capsomere in complex with the AAVR suggest that amino acid residues from different 2/3/5-fold surface loops are critical for this interaction.
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Creative Biogene's CAG-GFP AAV (Serotype AAV-BI30) exceeded our expectations in terms of purity and titer. It was critical for achieving consistent results across our cell lines in gene expression studies.
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