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mInsulin2-SaCas9 AAV (Serotype 9)

mInsulin2-SaCas9 AAV (Serotype 9)

Cat.No. :  AAV00357Z

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. AAV00357Z
Description Premade AAV particles in serotype 9 express Staphylococcus aureus Cas9 (SaCas9) from the mInsulin2 promoter.
Serotype AAV Serotype 9
Target Gene SaCas9
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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The mInsulin2-SaCas9 adeno-associated virus (AAV) serotype 9 is a scientifically engineered viral vector designed for gene editing applications. This pre-made AAV particle utilizes the Staphylococcus aureus Cas9 protein (often abbreviated as SaCas9), a smaller Cas9 ortholog that has high efficiency and fidelity in gene editing tasks. SaCas9 is smaller than the traditional SpCas9 and can therefore be packaged more efficiently in AAV vectors, enabling the co-delivery of additional regulatory elements when needed. SaCas9 is regulated by the mInsulin2 promoter. The mInsulin2 promoter refers to a specific DNA sequence that regulates the expression of the mouse insulin 2 gene. Promoters are critical DNA regions located upstream of a gene; they serve as binding sites for transcription factors and other proteins that control the initiation of transcription. In this context, the mInsulin2 promoter is responsible for controlling when and how much insulin the insulin 2 (Ins2) gene produces in response to various physiological signals. AAV serotype 9 has good tropism and can efficiently transduce a variety of cell types, especially in neural tissue and muscle, making AAV9 vectors very suitable for systemic and local delivery. This special vector design is suitable for studying gene function and regulation, which is expected to bring new insights into therapeutic development, especially in the field of endocrine and metabolic research affecting diabetes and related diseases.
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Customer Reviews
Work well

We appreciated their robust quality control process that ensured the vectors met high standards, a critical factor for the success of our gene therapy applications.

United States

01/26/2021

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