Transfected Stable Cell Lines
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Cat. No. : AAV00376Z
Serotype : AAV Serotype 9 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00376Z |
| Description | Premade AAV particles in serotype 9 express hM3D(Gq)-mCherry from the EF1a promoter. |
| Gene | hM3D(Gq)-mCherry |
| 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. |
EF1a-hM3D(Gq)-mCherry AAV (serotype 9) is a genetically engineered viral vector designed for advanced neurological research and therapeutic applications. This adeno-associated virus (AAV) belongs to serotype 9 and is known for its excellent transduction ability, capable of transducing a wide range of tissue types, with particular proficiency in the central nervous system. Its high efficiency in penetrating the blood-brain barrier makes it a valuable tool for delivering genetic material to neurons and other cells in the brain.
The construct within this specific AAV particle is designed to express the hM3D(Gq)-mCherry fusion protein. The hM3D(Gq) component is part of the designer G protein-coupled receptor (GPCR) in the DREADDs (Designer Receptors Activated Only by Designer Drugs) technology. This modified receptor is designed to be activated by an otherwise inert ligand, typically clozapine-N-oxide (CNO), allowing precise control of signaling pathways in receptor-expressing cells. Activation of hM3D(Gq) typically results in the stimulation of phospholipase C, which plays a key role in various intracellular signaling processes, leading to increased neural excitability. mCherry is a fluorescent protein that can be used as a reporter gene to facilitate visualization and confirmation of expression within target tissues. Scientists can use this property to ensure that AAV has successfully transduced the target area and evaluate the expression levels achieved.
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We observed exceptional transduction efficiency in our in vivo mouse models using this EF1a-hM3D(Gq)-mCherry AAV (Serotype 9). This efficiency was crucial for the success of our gene delivery experiments.
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