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Elastase I-SaCas9HF AAV (Serotype 9)

Elastase I-SaCas9HF AAV (Serotype 9)

Cat.No. :  AAV00362Z

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. AAV00362Z
Description Premade AAV particles in serotype 9 express high-fidelity Staphylococcus aureus Cas9 (SaCas9) from the Elastase I promoter.
Serotype AAV Serotype 9
Target Gene SaCas9HF
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 Elastase I-SaCas9HF AAV system is a versatile and powerful tool for precision genome engineering. AAV vectors are a top choice in both the clinical and research fields due to their relatively low immunogenicity and long-term expression capacity compared to other vector systems. In addition, the non-pathogenicity of AAV and the low risk of integration into the host genome make it a safer gene therapy alternative. The Elastase I-SaCas9HF AAV utilizes the serotype 9 variant, which is known for its broad tropism and ability to effectively target multiple tissues in vivo, especially muscle, heart, and neural tissues. The vector encodes a high-fidelity version of Staphylococcus aureus Cas9, called SaCas9HF, which is a powerful genome editing tool. The expression of SaCas9 is driven by the Elastase I promoter. The Elastase I promoter is a DNA sequence located at the beginning of the Elastase I gene, which is primarily expressed in the pancreas. The Elastase I promoter controls the expression of elastase, an enzyme involved in the digestion of proteins in the small intestine. In research, the Elastase I promoter is often used in genetic engineering and studies related to gene regulation and expression, especially for targeted gene expression to the pancreas in transgenic animals.
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Customer Reviews
Highly recommend for precision gene editing work.

The quality and purity of the Elastase I-SaCas9HF AAV (Serotype 9) vectors were exceptional, which translated into robust experimental findings. Highly recommend for precision gene editing work.

Germany

05/20/2023

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