Search Thermo Fisher Scientific
- Contact Us
- Quick Order
-
Don't have an account ? Create Account
Search Thermo Fisher Scientific
Applied Biosystems TaqMan Copy Number Assays employ TaqMan MGB probe chemistry to evaluate the copy number of genomic DNA targets using Applied Biosystems real-time PCR instruments and software. Together, the assays and the instrumentation can be used to obtain specific, reproducible, and easy-to-interpret copy number results. In addition, this method is fast and simple, and can be completed in hours rather than days, like traditional methods for analyzing copy number. The TaqMan Copy Number Assay workflow can be automated so that several hundred to thousands of samples can be processed in a single day. As the simplest method available to study copy number variation, TaqMan Copy Number Assays feature easy assay ordering and a simple workflow to enable quick results.
Use our Search Tool below to find the single tube assays you need.
Both custom assay options allow you to submit a target sequence to our TaqMan Assay design pipeline. Generate specific, reproducible and easy-to-interpret copy number results that provide a flexible targeted approach to copy number analysis and are suited for validation studies and large sample screens.
Order your TaqMan Copy Number Assays preplated into Fast or standard 96- or 384-well plates with the TaqMan Custom Plating Service. Save time and reduce the resources needed for large-scale experiments.
Run reference assays with copy number assays in duplex real-time PCR to detect and measure copy number variations in the human and mouse genomes.
Download your TaqMan documentation files
Brochure: TaqMan Assays for genetic variation research
Quick Reference Card: TaqMan Assays for genetic variation
Application Note: Design pipeline and validation of TaqMan Copy Number Assays
Product Bulletin: TaqMan Copy Number Assays
Product Overview: TaqMan Copy Number Assays
Poster: Coverage of the PharmaADME Consortium core marker list by TaqMan DME and Copy Number Assays
Identification of rare recurrent Copy Number Variants in high-risk autism families and their prevalence in a large ASD population
For Research Use Only. Not for use in diagnostic procedures.