Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : AAV00356Z
Serotype : AAV Serotype 9 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00356Z |
| Description | Premade AAV particles in serotype 9 express Staphylococcus aureus Cas9 (SaCas9) from the rInsulin2 promoter. |
| Gene | SaCas9 |
| Serotype | AAV Serotype 9 |
| 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. |
AAV (adeno-associated virus) vectors have become an important tool for gene therapy and genetic research due to their ability to infect a wide range of dividing and non-dividing cell types with minimal immune response. rInsulin2-SaCas9 AAV (serotype 9) is a unique vector that incorporates the Staphylococcus aureus Cas9 (SaCas9) gene editing protein driven by the rInsulin2 promoter. The advantage of choosing SaCas9 is that it is smaller than the more common SpyCas9 derived from Streptococcus pyogenes and can be more easily packaged within the AAV vector. This property makes SaCas9 an ideal tool for in vivo applications where vector capacity is limited.
The rInsulin2 promoter refers to a specific DNA region that regulates the expression of the rat insulin 2 gene. Promoters are DNA sequences located upstream of the start site of a gene and play a key role in controlling when and where a gene is activated. In the case of the rInsulin2 promoter, it is responsible for initiating transcription of the insulin 2 gene, primarily in pancreatic beta cells, where insulin is produced. The promoter contains a specific sequence that enables it to be recognized and bound by transcription factors, thereby initiating and regulating the transcription of the insulin 2 gene. The rInsulin2 promoter is used to specifically direct the expression of SaCas9.
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One of the best features is the rInsulin2-SaCas9 AAV (Serotype 9)’s targeting specificity, which significantly reduced off-target effects, thus improving the precision of our gene editing.
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