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GFP Adeno-Associated Virus ( AAV2-PPS )

GFP Adeno-Associated Virus ( AAV2-PPS )

Cat.No. :  AAV00442Z

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

Serotype:  AAV Serotype 2 Storage:  -80 ℃

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AAV Particle Information

Quality Control

Cat. No. AAV00442Z
Description This virus is a reporter AAV with capsid engineering / modification. GFP AAV2-PPS particles contain engineered capsid derived from AAV serotype 2 (AAV2) which has insertion of peptides DSPAHPS at I587. The target cell type of this capsid engineered AAV is central nervous system (CNS).
Reporter GFP
Serotype AAV Serotype 2
Target Gene GFP
Application

1. Determination of optimal MOI (multiplicity of infection), administration methods etc.

2. Detection of the infection efficiency of the AAV serotype against a specific cell type or tissue.

3. Using reporter genes to visualize the distribution and expression of AAV vectors in live animals, helping assess the biodistribution and persistence of gene delivery.

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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Customer Reviews

There is a particular need for new treatment options in medicine for neurovascular and neurological diseases, and gene therapy is a promising approach to meet this need. However, only a few vector systems are able to effectively transfer genes to the central nervous system (CNS), and none are specific. Adeno-associated virus (AAV)-based vectors are important candidates for clinical applications in neurological diseases because they can effectively transduce neural cells and have a favorable safety profile. Nonetheless, like most viral vectors, their natural tropism does not allow for specific transduction after systemic administration in vivo. AAV2-PPS particles are specifically engineered to incorporate a peptide sequence, specifically DSPAHPS, at site I587 of the viral capsid. This precise engineering enhances the ability of the virus to target specific cell types. Its ability to target the CNS, coupled with easy tracking via GFP, makes this engineered virus a powerful tool for basic research and the development of therapeutic strategies to treat CNS diseases. This innovative vector underscores the continued development and potential of AAV-based gene delivery systems to advance biomedicine.
Customer Q&As
What is GFP protein used for?

A: Green fluorescent protein (GFP) and its homologs are widely used as fluorescent markers of gene expression and for determination of protein localization and motility in living cells.

Why is adeno-associated virus used in gene therapy?

A: The unique life cycle of adeno-associated virus (AAV) and its ability to infect non-dividing and dividing cells and to sustain expression make it an attractive vector. Another attractive feature of wild-type viruses is the lack of overt pathogenicity.

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Customer Reviews
Exceptional Targeting Efficiency

The engineered capsid modification with the DSPAHPS peptide insertion at I587 ensures remarkable targeting precision, allowing us to achieve higher transduction rates in neuronal cells compared to other vectors we've used.

United States

01/07/2020

invaluable tool

The engineered capsid of the GFP AAV2-PPS demonstrated superior delivery and penetration into the central nervous system. This capability greatly enhances the efficacy of our experimental protocols, making it an invaluable tool for CNS-related research.

French

11/22/2022

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