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Frequently Asked Questions

Submicro Expression Array Detection Kits
* Which Submicro kit do I need?
* What is a dendrimer?
* How many dyes are on each 3DNA dendrimer molecule?
* How much "lot to lot" variation occurs in the number of dyes per dendrimer?
* With so many dyes attached to each 3DNA dendrimer, does quenching occur?
* Do you experience photobleaching with the 3DNA reagents?
* Can 3DNA dendrimers be used on membrane arrays?
* Will the 3DNA dendrimer without cDNA bind to specific sequences on my array?
* What is the shelf-life of the Submicro kit?
* I looked at the fluorescently-labeled Vial 1 reagent and it does not have any color?
* Which scanners are compatible with your product?
* What are the differences between the Submicro and Submicro EX kits?
* Can I use your kit for all species of RNA?
* Can I use the Submicro protocol with a Submicro EX kit, if I dilute the primer?
* Can I scale up the Submicro protocol?
* I currently use SuperScript II enzyme. Can I use my enzyme or do I have to use the one in your kit?
* What is the purpose of Vial 8 (anti-fade reagent) in your kit? Do I have to use it?
* Your protocol is designed for cDNA arrays. Can I use your product on oligo arrays?
* How much RNA should I use with your kit?
* Should I treat my RNA sample with DNAse?
* What is the best method to follow to purify my RNA for use with your kit?


General

* What is 3DNA™?
* How does 3DNA achieve this high performance?
* How can 3DNA benefit my research?
* What kind of signal enhancement can I expect?
* What applications are possible with 3DNA probes?

 



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