Oncology | Blood cancer

Your partner in oncohematology

QIAGEN’s oncohematology solutions bring innovation in molecular testing, faster and without compromise. We support your clinical cancer care and advancements in molecular research with a comprehensive assay, platform and service portfolio – from Sample to Insight.
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using real-time PCR

Sensitive JAK2 V617F mutation detection using real-time PCR

The ipsogen JAK2 RGQ PCR Kit is the only FDA-cleared kit for detection of the JAK2 V617F/G1849T allele, a World Health Organization (WHO) diagnostic criterion for myeloproliferative neoplasms (MPNs) (1).

Your partner for blood cancer companion diagnostics

Successful companion diagnostic (CDx) and drug co approval requires the right partner. QIAGEN has a proven track record in IVD development, global regulatory capabilities and global commercialization expertise.

Your partner for blood cancer  companion diagnostics
ipsogen real-time PCR blood cancer assays

Test with confidence

QIAGEN's extensive oncohematology portfolio includes multiple solutions for highly sensitive and accurate leukemia biomarker detection and/or quantification. Test with ipsogen, for results you can trust.

Maximize your blood cancer clinical research


1. Arber, D.A. et al. (2016) The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 127, 2391-2405.


ALL: Acute lymphoblastic leukemia; AML: Acute myeloid leukemia; CML: Chronic myeloid leukemia; CNV: Copy number variation; InDel: Inserstions/deletions; IS: International Scale; MPN: Myeloproliferative neoplasms; MRD: Minimal residual disease; NGS: Next-generation sequencing; Ph: Philadelphia chromosome; SNV: Single nucleotide variation.

The ipsogen JAK2 RGQ PCR Kit is intended for in vitro diagnostic use.

The CALR RGQ PCR Kit, ipsogen MPL W515L/K MutaScreen Kit , BCR-ABL1 Mbcr RGQ RT-PCR Kit, ipsogen BCR-ABL1 mbcr Kit, ipsogen PML-RARA kits, ipsogen NPM1 MutaScreen Kit and ipsogen NPM1 MutaQuant kits are for Research Use Only. Not for use in diagnostics procedures. No claim or representation is intended to provide information for the diagnosis, prevention, or treatment of a disease.

QIAseq Panels are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.

QCI Interpret is an evidence-based decision support software intended as an aid in the interpretation of variants observed in genomic next-generation sequencing data. The software evaluates genomic variants in the context of published biomedical literature, professional association guidelines, publicly available databases, annotations, drug labels, and clinical-trials. Based on this evaluation, the software proposes a classification and bibliographic references to aid in the interpretation of observed variants. The software is NOT intended as a primary diagnostic tool by physicians or to be used as a substitute for professional healthcare advice. Each laboratory is responsible for ensuring compliance with applicable international, national, and local clinical laboratory regulations and other specific accreditations requirements.

For up-to-date licensing information and product-specific disclaimers, see the respective QIAGEN kit handbook or user manual. QIAGEN kit handbooks and user manuals are available at www.qiagen.com or can be requested from QIAGEN Technical Services or your local distributor.