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GFP Adeno-Associated Virus ( AAV-NRTYS )

GFP Adeno-Associated Virus ( AAV-NRTYS )

Cat.No. :  AAV00479Z

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. AAV00479Z
Description This virus is a reporter AAV with capsid engineering / modification. GFP AAV-NRTYS particles contain engineered capsid derived from AAV serotype 2 (AAV2) which has insertion of peptides NRTYSSTSNSTSRSEWDNS at I588. The target cell type of this capsid engineered AAV is endothelial cells.
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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Background

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Customer Reviews

Vectors based on adeno-associated viruses (AAV) are considered safe and effective, and they have been used in many clinical trials. The various AAV serotypes vary greatly in tropism, but none are specific to a single tissue after systemic administration, which is the most advantageous mode of vector administration for most gene therapy applications. Mixing capsid subunits from different AAV serotypes can redirect and improve transduction of target tissues to some extent. However, due to the limited diversity of pre-existing capsid proteins, this approach rarely achieves true vector specificity. GFP AAV-NRTYS is a viral vector designed specifically for efficient gene delivery, especially targeting endothelial cells. The vector is a recombinant AAV with engineered capsids, derived from AAV serotype 2 (AAV2). The distinctive feature of this custom vector is the addition of a specific peptide sequence NRTYSSTSNSTSRSEWDNS at residue I588 of the capsid. This modification enhances the ability of the virus to transfect endothelial cells, a key cell type in the vasculature and in many pathological conditions such as cancer, cardiovascular disease, and inflammation.
Customer Q&As
Do AAVs cross the blood brain barrier?

A: Both AAV9 and AAV-rh10 are currently the gold standard capsids known to cross the blood-brain barrier (BBB) and are most commonly used for delivery to the central nervous system (CNS).

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Customer Reviews
Excellent choice

I've been using the GFP Adeno-Associated Virus (AAV-NRTYS) in my endothelial cell studies, and the results have been extraordinary.

Canada

04/24/2020

Great product!

The high transduction efficiency and strong GFP expression enable us to conduct precise and reproducible vascular studies.

Germany

12/02/2022

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