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CAG-Cre-GFP AAV (Serotype 1)

CAG-Cre-GFP AAV (Serotype 1)

Cat.No. :  AAV00073Z

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

Serotype:  AAV Serotype 1 Storage:  -80 ℃

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AAV Particle Information

Quality Control

Cat. No. AAV00073Z
Description CAG-Cre-GFP AAV (Serotype 1) is the serotype 1 (with Capsid from AAV1 and ITR from AAV2) which express Cre recombinase fusion with GFP under CAG (also known as CBA) promoter which is a combination of the cytomegalovirus (CMV) early enhancer element and chicken beta-actin promoter for high levels of gene expression in mammalian expression vectors. Used as a control.
Reporter GFP
Serotype AAV Serotype 1
Target Gene CAG-Cre-GFP
Product Type Adeno-associated virus
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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CAG-Cre-GFP AAV (serotype 1) is a powerful tool for precise manipulation of genetic sequences within mammalian cells in molecular biology and genetic research. This adeno-associated virus (AAV) vector combines elements of two different AAV serotypes: it utilizes the capsid of AAV1, known for its efficient gene delivery capabilities, especially in muscle and neural tissues, and the inverted terminal repeats (ITRs) of AAV2, which are essential for replication and packaging of the viral genome. The CAG promoter, a hybrid of the cytomegalovirus (CMV) enhancer and the chicken β-actin promoter, is a powerful and ubiquitous promoter that drives high levels of transgene expression in a variety of cell types. Its inclusion in this vector ensures efficient transcription of the Cre recombinase and the GFP (green fluorescent protein) gene in target cells. Cre recombinase is an enzyme that promotes site-specific recombination events between loxP sites. Incorporation of Cre into this AAV vector allows researchers to selectively manipulate the genome of host cells. This is often used in conditional knockout studies, where gene inactivation is desired in specific tissues or at a specific developmental stage. Additionally, a GFP reporter gene is included to allow for direct visualization and confirmation of transgene expression. GFP fluoresces brightly green when exposed to blue light, providing a reliable method for identifying infected cells and tracking gene expression in living tissues.
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Customer Reviews
Dependable tool

CAG-Cre-GFP AAV (Serotype 1) integrates seamlessly with our existing protocols, and the results are consistently reproducible. Our lab has seen significant advancements in our projects thanks to this dependable tool.

Germany

09/28/2020

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