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Syn-FLEX-NES-jRGECO1a AAV (Serotype 8)

Syn-FLEX-NES-jRGECO1a AAV (Serotype 8)

Cat.No. :  AAB0022

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. AAB0022
Description Premade AAV particles in serotype 8 containing Cre-dependent jRGECO1a under the control of a Syn promoter. The nuclear export signal (NES) directs export of proteins from the nucleus to the cytoplasm.
Serotype AAV Serotype 8
Tag jRGECO1a
Product Type Adeno-associated virus particles
Biosensor jRGECO1a-Red, improved SNR
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 ssDNA, non-enveloped, small (~26 nm in diameter), T = 1 virus of the genus Dependoparvovirus in the family Parvoviridae. Dependoparvovirus has been isolated from a variety of mammals, including humans, non-human primates, cattle, goats, pigs, sea lions, foxes, rodents, and bats. In addition, members of this genus have also been found in birds and reptiles. The structures of many AAV serotypes, variants, and isolated capsids have been determined by X-ray crystallography and/or cryo-electron microscopy (cryo-EM). All AAV capsid structures exhibit common features such as a channel at the 5-fold axis, protrusions around the 3-fold axis, and depressions around the 2-fold axis and 5-fold channel. The capsid is composed of three overlapping structural viral proteins (VPs), the minor proteins VP1 (~80 kDa) and VP2 (~65 kDa), and the major protein VP3 (~60 kDa). A total of 60 VPs are contained in the capsid in a ratio of approximately 1:1:10. The amino acid sequence of VP3 is identical to the two minor capsid proteins, while VP2 has an N-terminal region shared with VP1 (the VP1/2 common region). The VP1/2 common region contains nuclear localization motifs that have been shown to play an important role in localizing incoming capsids to the nucleus following infection of cells with AAV. In addition, VP1 contains a unique N-terminal sequence, called the VP1 unique region (VP1u), which contains a phospholipase A2 domain that is required for endosome escape during cellular trafficking via the intralysosomal pathway. The N-termini of VP1 and VP2 are thought to be located inside the capsid and are externalized after structural rearrangements following endosomal acidification during cellular trafficking.
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Customer Reviews
High-Level Expression

The Syn-FLEX-NES-jRGECO1a AAV (Serotype 8) delivered exceptional gene expression levels in our neuronal culture systems. It has significantly aided in our research by providing clear, reliable results.

Canada

07/13/2021

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