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Genetics

Innovative solutions that empower researchers, from fragile X syndrome to CFTR to SMN1/2.

AmplideX Genetics assay kits for Inherited Disorders
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Oncology

Solving complex molecular challenges, from chronic myeloid leukemia (CML) to solid tumors.

Learn about QuantideX BCR-ABL Kits & CML Monitoring
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Molecular Quality Controls

Custom & Ready-to-Order Molecular Quality Controls & OEM Services

Learn about our molecular quality controls
Spotlight

Join us at the European Society of Human Genetics (ESHG) Conference 2023!

Asuragen, a Bio-Techne brand’s unique and proprietary AmplideX® and QuantideX® chemistries power simple and streamlined solutions for analysis of complex genomic targets. Visit us at stand #268

Learn more about Asuragen at ESHG 2023
Spotlight

Asuragen to showcase innovative diagnostics lab solutions at AMP 2022 Conference

At AMP, Asuragen will host two educational workshops, one focused on a streamlined workflow and equitable testing approach for genetic testing and the other on rapid development of molecular controls for emerging diseases. Scientists from the company will also present several posters with updates about clinical tests based on nanopore sequencing technology, molecular controls for SARS-CoV-2 testing, and more.

Learn more about Asuragen at AMP 2022
Spotlight

Asuragen Launches New Kit to Enable Broader Coverage of Gene Variants Linked to Cystic Fibrosis

CFTR testing kit with streamlined workflow delivers reliable results in less than five hours

Learn More about our CFTR testing kit
Spotlight

Asuragen Announces Launch of AmplideX® PCR/CE SMN1/2 Plus Kit

The AmplideX® PCR/CE SMN1/2 Plus Kit is a clinical research tool providing the most comprehensive analysis of SMN1 and SMN2 currently available from a commercial kit.

Learn more about our SMN1/2 Plus kit
Spotlight

Asuragen Expands Genetic Portfolio with Launch of AmplideX® PCR/CE HTT Kit

The AmplideX® PCR/CE HTT Kit is a simple, robust, and reliable test for the detection of CAG trinucleotide repeats within the HTT gene, aberrations which are associated with the development of Huntington’s Disease (HD).

Read more about our HTT kit

The Latest from Asuragen

Behind the Mystery of Fragile X Syndrome

Fragile X syndrome is a genetic disorder that is caused by a gene mutation on the X chromosome. Symptoms frequently include developmental delays, intellectual disabilities, and behavioral issues. Carriers for Fragile X don’t have Fragile X syndrome; however, they do have an increased chance of certain medical issues. Testing for Fragile X syndrome is important, especially for women who are pregnant or plan to become pregnant. Learn more about Fragile X from Ilana Garber, who shares her and her son Yaron’s journey with Fragile X syndrome as well as from Dr. Tamar Goldwaser, an OBGYN and medical geneticist.

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