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AAV9-αMHC-Cre

AAV9-αMHC-Cre

Cat.No. :  AAV00266Z

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

Serotype:  AAV Serotype 9 Storage:  -80 ℃

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AAV Particle Information

Quality Control

Cat. No. AAV00266Z
Description AAV serotype 9 particles contain Cre recombinase under the mouse alpha myosin heavy chain (αMHC) promoter for specific expression in cardiac muscle cells.
Serotype AAV Serotype 9
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 small, non-enveloped, single-stranded DNA virus that is endemic and non-pathogenic in humans. Multiple AAV serotypes are known, each with its own tropism for specific cell types. AAV can be used as a gene therapy vector by removing the viral genome and replacing it with an expression cassette containing tissue-selective regulatory elements and the gene of interest. There is interest in using AAV9 to treat muscle and neurological diseases. Currently, a clinical trial is being developed to administer rAAV9-hGAA to patients with late-onset Pompe disease using muscle transduction with AAV9. Additionally, a clinical trial is currently underway to treat Duchenne muscular dystrophy using AAV9. The FDA-approved drug Zolgensma also utilizes the AAV9 capsid to deliver a functional copy of the smn1 gene to motor neurons in patients with spinal muscular atrophy.
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Customer Reviews
Efficient Cardiac Targeting

AAV9-αMHC-Cre's highly efficient targeting to cardiac tissues ensures precise Cre-recombinase activity, significantly enhancing the success rates of my experiments.

Germany

09/25/2024

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