The ChromoQuant AZF PCR kit will diagnose male infertility due to microdeletions in the Y chromosome;
AZFa, AZFb, AZFc and terminal deletion
CE-marked for IVD use
· For routine diagnostics
· Developed in accordance with EAA/EMQN guidelines 2013
· Basic and Extension set of non-polymorfic markers
· Heterochromatin marker for analysis of terminal deletion
· Distal and proximal break point analysis
· GeneMapper and GeneMarker panel templates are available
· ChromoQuant® is CE marked for IVD use and produced according to ISO13485
Product Information
Intended Use
Diagnosis of micro deletions in the Y chromosome
AZFa, AZFb and AZFc
Part no.
800.001-32
Ready to use
Add only DNA. Ready for PCR. Taq polymerase included
No. of tests / Kit size
32 tests for AZFa, b, c – basic set
10 tests for extended diagnosis of AZFa and AZFb
Basic set of markers
7 non polymorphic markers + 2 controls will detect more than 95% of all deletions reported in the literature. Sufficient for routine diagnosis. sY160 included.
Extension set of markers -
AZFa extension set: 4 non polymorphic markers + 2 controls
AZFb extension set: 4 non polymorphic markers + 2 controls
PCR / Capillary - The basic set of markers for AZFa, b and c is analysed in one PCR tube and one capillary. This set of markers gives a diagnosis for deletions in the AZFa, b, c and terminal region. The AZFa and AZFb extensions sets are used to indentify break points in the AZFa and the AZFb region respectively.
17 markers in total
Taq polymerase - Included
Capillary Electrophoresis
Validated Genetic Analysers
ABI 310, 3100, 3130, 3500, 3730