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U6-shRNA-GFP AAV (Serotype 1)

U6-shRNA-GFP AAV (Serotype 1)

Cat.No. :  AAV00071Z

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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Cat. No. AAV00071Z
Description U6-shRNA-GFP AAV (Serotype 1) is the serotype 2/1 (with Caspid from AAV1 and ITR from AAV2) which express scramble shRNA under U6 promoter with co-expression of GFP as reporter under CMV promoter. This product used in the gene knockdown experiments as a control in cultured cells and animal experiments.
Serotype AAV Serotype 1
Target Gene U6-shRNA-GFP
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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U6-shRNA-GFP AAV (serotype 1) is an advanced tool in the field of genetic research, particularly useful for studying gene function through knockout experiments. This vector is a hybrid of serotypes 2 and 1, combining the inverted terminal repeats (ITRs) of adeno-associated virus type 2 (AAV2) and the capsid of AAV type 1 (AAV1). This configuration is specifically designed to take advantage of the unique advantages offered by each serotype, optimizing packaging and delivery efficiency in target tissues. The core feature of this vector is the expression of scrambled short hairpin RNA (shRNA) under the control of the U6 promoter. The U6 promoter is known for its strong and ubiquitous expression, ensuring efficient transcription of shRNA in a variety of cell types. By expressing a non-targeting, scrambled shRNA, this AAV vector can be used as a control in experiments designed to evaluate the effects of a specific shRNA sequence on gene silencing. Importantly, scrambled shRNAs have no known targets in the genome, which helps determine whether observed phenotypic changes are due to targeted gene knockdown induced by the specific shRNA and not off-target effects or vector-related artifacts.
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Customer Reviews
Great Customer Support

The customer support team has been incredibly helpful, quickly addressing any questions we had during our initial setup. Highly recommend!

Canada

07/01/2023

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