AAV Serotype Blast™ Kit, High Titer
Unit
9 x 100 µl, 1013 GC/mL
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Cat. No.
AAV100
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Name
AAV Serotype Blast™ Kit, High Titer
Unit
9 x 100 µl, 1013 GC/mL
Description
It has been well established that many variables can affect AAV transduction efficiency: different serotypes, cell types, multiciplicity of infection (MOI), etc. The AAV Serotypes Blast™ Kit, High Titer is a sample of different premade high titer AAV of different serotypes, developed to simplify the transduction optimization process. This starter kit consists of control viruses of 9 common serotypes expressing GFP signals, allowing you to save time in finding the AAV serotype that works best for your in vivo model. To find the optimal conditions for your experiment, all you need to do is inject the AAV with the appropriate MOI and monitor GFP signals.
Advantages of abm’s AAV Serotype Blast™ Kit, High Titer
Serotype 1-9 available in the kit for testing
The kit is easy to use
Simplify your transduction optimization process
Helps you to draw accurate conclusions on suitable serotypes for your cell lines
This AAV serotype starter Kit has a large range of the cell types which can be tested against
Saves you time for your research
Vector
pAAV-G-CMV-GFP-Blank Amp
Material Citation
If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. AAV100
There are no Documents for this product yet!
Ellis, et al. " A survey of ex vivo/in vitro transduction efficiency of mammalian primary cells and cell lines with Nine natural adeno-associated virus (AAV1-9) and one engineered adeno-associated virus serotype." Virology Journal 10(74): (2013).
Schultz, B.R. et al. " Recombinant Adeno-associated Virus Transduction and Integration." The American Society of Gene Therapy 16(7):1189-1199 (2008). DOI: doi:10.1038/mt.2008.103.
Pajusola, K. et al. " Cell-Type-Specific Characteristics Modulate the Transduction Efficiency of Adeno-Associated Virus Type 2 and Restrain Infection of Endothelial Cells." Journal of Virology 76(22):11530-11540 (2002). DOI: 10.1128/JVI.76.22.11530–11540.2002.
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