Transfected Stable Cell Lines
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Cat. No. : AAV00375Z
Serotype : AAV Serotype 9 Storage : -80 ℃
Titer: Size:
| Cat. No. | AAV00375Z |
| Description | Premade AAV particles in serotype 9 express HA-hM3D(Gq)-mCherry from the EF1a promoter. |
| Gene | HA-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-HA-hM3D(Gq)-mCherry AAV (serotype 9) is a recombinant adeno-associated virus widely used in neuroscience and gene therapy research. AAV vectors are popular for their ability to safely and efficiently deliver genetic material into host cells. Among the various serotypes of AAV, serotype 9 is particularly known for its excellent ability to penetrate the blood-brain barrier, making it a valuable tool for neuronal targeting in vivo.
The EF1a promoter is a potent and ubiquitous promoter known for driving high levels of transgene expression in a variety of cell types, which is critical to ensure that the gene of interest is expressed in the target tissue. The HA tag provides a convenient detection and purification method due to its reactivity with HA-specific antibodies.
The hM3D(Gq) component refers to a specially designed G protein-coupled receptor (DREADD) that is designed to be activated by the otherwise pharmacologically inert compound clozapine nitro-oxide (CNO). This technology enables spatial and temporal control of neuronal activity, allowing researchers to manipulate cellular signaling pathways in vivo with high precision. Specifically, hM3D(Gq) is a modified human muscarinic receptor that upon activation stimulates intracellular signaling cascades through the Gq protein, typically leading to excitatory cellular responses. The construct also contains an mCherry fluorescent protein that acts as a versatile reporter gene. The bright red fluorescence emitted by mCherry allows researchers to visualize and confirm the expression and localization of the viral construct within host tissues.
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The quality of this AAV vector exceeded my expectations. The purity and concentration were spot-on, making it perfect for our neuronal expression studies.
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