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AAV6-CMV-FLPo

AAV6-CMV-FLPo

Cat.No. :  AAV00210Z

Titer: ≥1x10^12 GC/mL / ≥1x10^13 GC/mL Size: 30 ul/100 ul/500 ul/1 ml

Serotype:  AAV Serotype 6 Storage:  -80 ℃

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AAV Particle Information

Quality Control

Cat. No. AAV00210Z
Description AAV serotype 6 particles contain FLPo recombinase under CMV promoter.
Serotype AAV Serotype 6
Titer Varies lot by lot, typically ≥1x10^12 GC/mL
Size Varies lot by lot, for example, 30 μL, 50 μL, 100 μL etc.
Storage Store at -80℃. Avoid multiple freeze/thaw cycles.
Shipping Frozen on dry ice
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.
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Adeno-associated virus (AAV) is a non-enveloped, single-stranded DNA virus belonging to the genus Dependoparvovirus of the family Parvoviridae. Upon co-infection with a helper virus such as adenovirus, herpes virus, or papillomavirus, AAV switches from a latent to a lytic phase, hijacking the host cell machinery. The AAV capsid consists of 60 capsid monomers, VP1, VP2, and VP3, in a 1:1:10 ratio, packaging a 4.7 kb single-stranded genome. The AAV genome encodes the replication (rep), capsid (cap), and assembly activation protein (AAP) open reading frames (ORFs) flanked by inverted terminal repeats (ITRs), which are the only requirement for genome packaging. Therefore, large portions of the genome can be replaced by foreign DNA sequences and packaged within the AAV capsid to create recombinant vectors in vitro and in vivo. Some recombinant AAV serotypes appear to be secreted into the cell culture medium prior to lysis, although the efficiency varies. Unlike other autonomous parvoviruses that undergo a lytic cycle, wild-type AAV does not induce a significant cytopathic effect (CPE), and therefore, extracellular egress of virions is thought to be driven primarily by overexpression of adenoviral or herpesvirus proteins.
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Customer Reviews
Exceptional Efficiency

We’ve used the AAV6-CMV-FLPo vector in multiple experiments. The transfection results were consistent and robust, allowing us to achieve our research goals seamlessly.

French

01/25/2020

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