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CAG-ChR2-YFP AAV (Serotype 6)

CAG-ChR2-YFP AAV (Serotype 6)

Cat.No. :  AAV00095Z

Titer: ≥1x10^12 GC/mL / ≥1x10^13 GC/mL Size: 30 ul/100 ul/500 ul/1 ml

Serotype:  AAV Serotype 6 Storage:  -80 ℃

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Cat. No. AAV00095Z
Description CAG-ChR2-YFP AAV (Serotype 6) is the serotype 6 AAV which express Channelrhodopsin-2 under CAG promoter with YFP tag. Channelrhodopsins are a subfamily of opsin proteins that function as light-gated ion channels and very useful for many bioengineering and neuroscience applications such as photostimulation of neurons for probing of neural circuits. Using a Yellow Fluorescent Protein (YFP) tagged ChR2, light-stimulated axons and synapses can be identified in intact brain tissue. This is useful to study the molecular events during the induction of synaptic plasticity. ChR2 has also been used to map long-range connections from one side of the brain to the other, and to map the spatial location of specific inputs on the dendritic tree of individual neurons.
Serotype AAV Serotype 6
Target Gene CAG-ChR2-YFP
Product Type Adeno-associated virus
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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Channelrhodopsin-2 (ChR2) is a blue light-activated membrane protein and ion channel that belongs to the channelrhodopsin subfamily of retinoic acid. ChR2 is derived from the green alga Chlamydomonas reinhardtii and is widely known for its key role in optogenetics. Functionally, ChR2 acts as a light-gated cation channel that allows ions such as sodium (Na+), potassium (K+), and calcium (Ca2+) to cross the cell membrane when exposed to blue light (primarily around 480 nm). The opening of this channel results in a change in membrane potential, allowing researchers to effectively control the electrical activity of neurons with high temporal precision in the millisecond range. The direct opening of the ion channel (a feature that differs from typical G protein-coupled receptors) enables ChR2 to rapidly depolarize cells, making it very useful in experiments aimed at understanding brain function and therapeutic interventions. The discovery and use of ChR2 has dramatically changed neuroscience. By incorporating ChR2 into specific neural populations, researchers can optically stimulate neurons in a controlled manner, facilitating the study of neural circuits and brain function. One of the major breakthroughs achieved with ChR2 is the mapping and control of neural networks, which has provided insights into diseases such as epilepsy, Parkinson's disease, and other neurodegenerative disorders.
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Reliable tool

Whether used in rodent models or in vitro neuron cultures, CAG-ChR2-YFP AAV (Serotype 6) consistently produces reliable results.

French

07/24/2024

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