Among male infer•tility patients caused by sp§§ermatogenesis disorders, the incidence $©of Y chromosome microdeletions ÷ ☆is second only to Klinefelter ’s syndrome₽∞δ (Klinefelter ’s syndrome) and is t>↑↑he second most important genetic factor. This ♠≤≈kit is used for rapiπλd detection of microdel≥ ∏etions of 15 sequence tags on δ®•the AZFa, AZFb and AZFc loci of π♠∞the Y chromosome AZF (AzoospermiaFactor) gene f✔α₹amily from male anticoagulated peripheral whol∞≤e blood.
To provide a molecular basis for diagnosis♥ of male infertility, to avoid unnecessary medicaδ§ tion or surgical treatment;
To provide guidance for clinic₩↓ally assisted reprod←∏®uction (e.g. injection in monosp♦erm follicle);
Identify the Y chromosome AZF£♣ micromissarea to provide a basis f★γ'<or selecting the right clinical treatment.↕×÷
The 2013 edition of the Europe®®an Andrology Association (EAA) and the™ European Molecular Genetic Diagε¥↑←nostic Quality Alliance↔'≥ (EMQN) released guidelines for the detection ★β≠€of Y chromosome microdeletions, recomm ≤✔£ending the detection of 6 STS sites.
Premarital examination and risk ass♦☆essment
Screening of causes ofλ↔ infertility patients
Detection of specimens: Anticoagulant whole blood or genomic δ×®DNA
Technical principle:Multiplex-PCR
Packing size:25tests / kit
Category: In vitro diagnostic reagents
Suitable instruments"→∑: Gene amplification instrument, electrophores®₽®←is instrument
Date:2020-03-26
Date:2020-03-30
Date:2020-03-17
Date:2020-03-11
Date:2020-03-03
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