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"I designed SYBR Green primers for 5 different genes using Beacon Designer. They all worked well and I am extremely pleased with the results." -Dr. Yulia Koryakina, University of Virginia, US.
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"We love your program - it has saved time in that we don't have to use 3 or 4 different programs to determine how well the probes we have designed will bind to other sequences. And it has saved money because I don't have to purchase several expensive labeled probes to test which one will work the best. With Beacon Designer™ 2, we can design specific probes efficiently and with the multiplex function save even more time and feel confident about the results. Certainly, Beacon Designer™ 2 will be able to design effective probes for detection of single base pair differences." -Dr. Gale Newman, Dept. Micro, Biochem, Immuno Morehouse School of Medicine, Atlanta, GA.
![PRIMERPLEX中文版使用教程](//l.b2b168.com/2021/09/27/17/202109271702134038204.jpg)
Beacon Designer™
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"I designed multiple qPCR assays using Beacon Designer and it worked perfectly for us! The features such as secondary structure search, blast search were very useful in selecting highly specific probes for our experiment" - Dr. Zhanhua Tao, Guangxi Academy of Sciences, China.
![PRIMERPLEX中文版使用教程](//l.b2b168.com/2019/07/19/15/201907191511177039654.jpg)
Edit Template Sequence
The template sequence is editable and can be changed by a user. Bases can be modified using the standard Cut/Copy/Paste functions. Unwanted regions of sequences can be removed by using the Delete button. Users can comment or annotate a sequence and save them for future reference.
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