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. : AAV00079Z
Serotype : AAV Serotype 2 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00079Z |
| Description | U6-shRNA-GFP AAV (Serotype 2) is the serotype 2 AAV which expresses scramble shRNA under U6 promoter with co-expression of GFP as reporter under CMV promoter. This product used in the gene knockdown experiments as a control in cultured cells and animal experiments. |
| Product Type | Adeno-associated virus |
| Gene | U6-shRNA-GFP |
| Serotype | AAV Serotype 2 |
| 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. |
U6-shRNA-GFP AAV (serotype 2) is a recombinant adeno-associated virus (AAV) vector specifically tailored for gene silencing research applications. This vector is engineered from serotype 2 of the AAV family to express random short hairpin RNAs (shRNAs) driven by the U6 promoter. It also co-expresses green fluorescent protein (GFP) as a reporter gene under the control of a cytomegalovirus (CMV) promoter.
The U6 promoter is known for its strong and ubiquitous expression in mammalian cells, making it an ideal driver of small hairpin RNA (shRNA) transcription. shRNAs are designed to be complementary to specific messenger RNA (mRNA) targets, thereby achieving RNA interference (RNAi). This RNAi mechanism effectively silences the expression of a target gene by promoting the degradation of its mRNA, thereby preventing the translation and production of the protein associated with that gene. The primary application of this AAV construct is as a control in gene knockdown experiments. By using random shRNAs, which do not target any specific mRNA within the host system, researchers can effectively demonstrate that changes observed in experimental outcomes are specific to the knockdown of their gene of interest and are not off-target or accidental results.
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The scramble shRNA provides a reliable control, and the GFP fluorescence is bright and easily detectable, aiding in effective experimental documentation.
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