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Syn-FLEX-GCaMP6m AAV (Serotype 8)

Syn-FLEX-GCaMP6m AAV (Serotype 8)

Cat.No. :  AAB0027

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

Serotype:  AAV Serotype 8 Storage:  -80 ℃

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AAV Particle Information

Quality Control

Cat. No. AAB0027
Description Premade AAV particles in serotype 8 containing Cre-dependent GCaMP6m under the control of a Syn promoter.
Serotype AAV Serotype 8
Tag GCaMP6m
Product Type Adeno-associated virus particles
Biosensor GCaMP6m-Improved SNR, intermediate kinetics; Green indicator
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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AAVs are small viruses (25 nanometers) of the genus Dependovirus in the family Parvoviridae, which indicates that they are dependent on a helper virus for efficient infection. These viruses have a non-enveloped capsid and store their genetic material in the form of single-stranded DNA. AAVs rely on helper viruses (such as adenovirus and herpes simplex virus) for replication and can infect both dividing and non-dividing cells. These properties make them potential agents for gene therapy of post-mitotic cells such as neurons. The 4.7 kb genome of AAV consists of ORFs containing the rep gene encoding proteins involved in viral replication, the cap gene encoding structural proteins required for capsid formation, and the aap gene required for the final assembly of capsid proteins. These ORFs are interlaced with two ITRs, which are cis-acting elements required for viral replication and packaging. Depending on the presence or absence of a helper virus, these viruses undergo either a lytic or lysogenic cycle, respectively. In the lytic cycle, the virus replicates its genome with the help of the host DNA polymerase and then produces virions. For the lysogenic cycle, the virus integrates into the host genome in a site-specific manner and requires helper virus rescue to return to the lytic state. For gene therapy, recombinant AAV vectors are constructed by replacing the ORF with the gene of choice and retaining the ITR. The helper functions required to maintain the lytic cycle are provided by co-transfection of plasmids containing the genes that confer these requirements.
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Customer Reviews
Versatile and Effective

I’ve used the Syn-FLEX-GCaMP6m AAV (Serotype 8) in a range of experimental setups, and its versatility is unmatched. Whether in vivo or in vitro, the expression level and activity detection are both excellent.

United States

09/05/2020

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