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AAV1-CAG-iCre

For research use only. Not intended for any clinical use.

Cat. No. :   AAV00131Z

Serotype :   AAV Serotype 1 Storage :   -80 ℃

Titer: Size:

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Virus Particles Information

Quality Control

Cat. No. AAV00131Z
Description AAV serotype 1 particles contain codon-improved Cre (iCre) 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.
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Adeno-associated virus (AAV) is a non-pathogenic member of the Parvoviridae family, belonging to the genus Dependovirus, and requires a viral helper function such as adenovirus or herpesvirus for infection. Twelve different AAV serotypes and more than 100 genomic isolates have been reported. There has been a great deal of interest in its development as a gene delivery vector, and many studies have shown that each virus has unique cell transduction properties.

AAV packages a genome of approximately 4.7 kb in an icosahedral capsid (T = 1), assembled from 60 capsid VP monomers with a diameter of approximately 260 Å. The capsid consists of three VPs: VP1, VP2, and VP3. VP1 contains the entire VP2 sequence plus a unique N-terminal region of approximately 137 amino acids (VP1u), while the VP2 protein contains the entire VP3 sequence plus an N-terminal region of approximately 65 amino acids (VP1/2 common region). VP3 is the major capsid protein, accounting for approximately 50 of the 60 capsid monomers, while gel densitometry studies have determined that there are approximately 5 copies of each of VP1 and VP2 per capsid (thus a 1:1:10 ratio of VP1:VP2:VP3). The three-dimensional structures of several AAV serotypes, including AAV1, AAV2, AAV3b, AAV4, AAV5, AAV6, AAV7, AAV8, and AAV9, have been determined by cryo-electron microscopy (cryo-EM) and image reconstruction and/or X-ray crystallography.

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User-Friendly Protocols

The detailed protocols provided were easy to follow, reducing our experimental setup time. Even team members new to the technology managed to use it effortlessly.

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