TaqMan™ Drug Metabolism Genotyping Assay
TaqMan™ Drug Metabolism Genotyping Assay
Applied Biosystems™

TaqMan™ Drug Metabolism Genotyping Assay

Green features
Applied Biosystems TaqMan Drug Metabolism Genotyping Assays use gold-standard TaqMan 5´-nuclease chemistry for amplifying and detecting specific SNP alleles, multi-nucleotideRead more
Have Questions?
Catalog number 4362691
Price (USD)
497.00
Each
Order now
Applied Biosystems TaqMan Drug Metabolism Genotyping Assays use gold-standard TaqMan 5´-nuclease chemistry for amplifying and detecting specific SNP alleles, multi-nucleotide polymorphisms (MNPs), and insertion/deletions (InDels) in genes associated with drug metabolism. The predesigned TaqMan Drug Metabolism Genotyping Assay collection consists of more than 2,600 assays that target high-value pharmacogenetic markers in 221 drug metabolism enzyme (DME) and associated transporter genes.

Benefits:
• Enables accurate detection of biologically important polymorphisms with roles in drug metabolism and transport
• Select individual assays for your drug metabolism studies, with flexibility and ease
• Find the right content in our comprehensive collection, with 95% coverage of ADME core markers
• Work confidently; our bioinformatics mapping, design, and in silico QC means you are studying the right SNP
• Get started immediately with ready-to-use assays delivered in as little as one day

Approximate ship time
1–2 days in North America and 3–5 days in Europe*

Every TaqMan Drug Metabolism Genotyping Assay in our collection has been functionally tested using genomic DNA samples from 180 individuals representing four different ethnic groups. The DME assay targets were derived from public databases, consortiums, and published articles. To enable easy identification, these assays have been mapped to the common public allele nomenclature websites where possible.

TaqMan SNP Genotyping Assays require only three reaction components for PCR: purified genomic DNA (1–20 ng), the assay solution, and TaqMan Genotyping Master Mix (or another compatible master mix) (sold separately).

All assay designs are the product of our bioinformatics pipeline, optimized over the course of more than a decade by leveraging manufacturing and assay performance data. TaqMan Assays have been cited in over 40,000 publications and are backed by more than 350 patents.

All of our predesigned TaqMan Assays are covered by the TaqMan Assays qPCR Guarantee.**

Recommended master mix (sold separately): TaqMan Genotyping Master Mix

*Our most popular assays are stocked in North America and Europe for overnight delivery where possible. If an assay is out of stock, it may take an additional 3–5 business days for delivery.

**Terms and conditions apply. For complete details, go to www.thermofisher.com/taqmanguarantee.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Concentration20X
TypeReagent
Label or DyeFAM, VIC
Product LineTaqMan™
Quantity150 reactions, Inventoried
Shipping ConditionRoom Temperature
SpeciesHuman
Target GeneAssays for 220 drug metabolism and transporter genes are available
FormFrozen
Unit SizeEach
Contents & Storage
1 tube containing a 20X mix of pre-formulated assay (2 probes and 2 primers).

Store at -15 to -25°C.

Frequently asked questions (FAQs)

How do I set up a reference panel in the TaqMan Genotyper Software?

A reference panel is helpful in large studies to mark your reference samples. Please follow the directions here on how to set up a reference panel.

How do I enter the polymorphism sequence information (i.e., A, C, G, T) for my assays, and where is this info displayed in the TaqMan Genotyper Software?

The polymorphism sequence info can be entered into the software through Setup >Assays. You can import an assay information file (AIF) that contains this info for your assays (AIFs are shipped with assay orders), or manually enter this info for each assay using the edit assay feature. The polymorphism sequence info will be displayed in the assays table under allele1 base and allele2 base, in the results table in the calls column, in the cluster plot display in the x-axis and y-axis titles, and in the export files as genotypes. If no sequence information is entered for an assay, the default display for genotype calls will use the dye names, such as VIC/VIC, VIC/FAM or FAM/FAM dyes.

What is the bookmarking feature in the TaqMan Genotyper Software, and how would I use it?

Bookmarking is a unique feature in TaqMan Genotyper Software that allows you to tag a data point or well while reviewing results in a Study. For example, in reviewing a cluster plot for an assay, a data point is observed to be somewhat between clusters. You can set a bookmark for this data point to denote this well for further investigation. The bookmark persists between the Results workspace and Quality Control workspace, so you can easily identify the data point in a cluster plot, experiment plate view, or on the samples tab. Bookmarks are cleared upon exit from a Study or exit from the application.

I am getting the message: "An error has occurred. See the log file C:\ProgramFiles\Applied Biosystems\TaqMan Genotyper\config\eclipse\1363113099385.log." How can I fix this?

1.Go to the Start button, then Programs, then TaqMan Genotyper Software
2.Right-click on the program and choose “Run as Administrator”
3.If that does not work, go back to the same menu and choose “Properties”
4.Choose the “Compatibility” tab, and check “Run this program as administrator”
5.Click “Apply”
6.You may+C69 have to restart the computer for the settings to apply

Can I delete an assay or sample from my qPCR study?

An assay or sample may be deleted from a study only if there is no data or wells associated with it. Upon import of an experiment, the software collects all the assays and samples from the plate and lists them in the Setup > Assays or Setup > Samples workspaces. The assays and samples are stored in these workspaces as a library, and remain there even if you delete the experiment from the Study. Deleting the experiment will remove any data (wells) associated with the assays or samples, but not the assays or samples from the library. The assays and samples must then be deleted from these workspaces to remove them from the Study.