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Custom miRCURY LNA™ Detection Probes

Ina K. Dahlsveen, Product manager Take advantage of Exiqon’s expertise in designing LNA™-enhanced detection probes targeting custom RNA sequences


Ina K. Dahlsveen, Ph.D., Product ManagerBack
  • Unmatched detection of small RNA molecules by in situ hybridization and Northern blotting
  • Superior specificity and sensitivity
  • Designed by our expert team for optimal LNA™ content and positioning
  • Minimal secondary structure and self-complementarity

Coverage

Our custom detection probes are available with a selection of 3’ and 5’ labels (DIG*, biotin, fluorescein, amino). “Ready-to-label” probes designed for custom labeling are also available. For ordering, price information and requests for alternative labels, please contact us.

In designing a probe, we recommend using sequences 20-25 nucleotides in length. A probe of this length uses the advantages of the LNA™ technology by resulting in high melting temperatures (between 70-85°C), good mismatch discrimination, and high binding specificity, while avoiding unacceptable secondary structure and self-complementarity. However, slightly shorter or longer probes can often be designed within the standard design criteria.

Note

Before submitting your order, please check if a pre-designed detection probe targeting your sequence is available . Pre-designed miRCURY LNA™ microRNA Detection Probes are available for all microRNA sequences annotated in miRBase.

*Licensed from Roche Diagnostics GmbH


Before submitting your order, please . Pre-designed miRCURY LNA™ microRNA Detection Probes are available for all microRNA sequences annotated in miRBase.
"I was intrigued by this interesting technology, which is very different from other available technologies."

Dr. Mircea Ivan at Indiana University School of Medicine studies the role of microRNAs in hypoxia. Here he describes why his lab chose Exiqon's detection probes.

Read full story...


“We got some beautiful data and spectacular images”

"We generated a complete catalogue of images showing the temporal and spatial expression patterns of 115 conserved microRNAs in zebrafish embryos."

Prof Ronald H. A. Plasterk, Hubrecht Laboratory, The Netherlands



Dylan Sweetman “Following the success of LNA™ probes as demonstrated in Plasterk’s lab, we decided to take the same approach”

Dr. Dylan Sweetman is working in Dr. Andrea Münsterberg’s group at the University of East Anglia, School of Biological Sciences. The group investigates cellular and molecular mechanisms that underlie embryonic development.


Parker Antin “LNA™ technology is superior to any other for the detection of small RNA species”

Dr. Parker Antin’s lab at the University of Arizona runs a large scale in situ hybridization database project to determine the expression patterns for all differentially expressed genes in the chicken embryo. Find out what the challenges were with this huge project and how they were overcome.

This is a custom LNA™ product. Please contact us for further information and ordering.
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