Aneuploidy Detection Kit
Aneuploidy is one of the main causes of birth defects. The common aneuploidy includes 21 trisomy, 18 trisomy, 13 trisomy and X/Y chromosome abnormalities, which accounts for 95% of overall abnormal chromosome numbers in newborns.
Our QF-PCR assay is performed using several selected highly polymorphic STR markers mapped on chromosomes 13, 18, 21, X and Y, together with the non-polymorphic AMXY (amelogenin) and SRY sequences for sample contamination detection.
Features
■ Accurate:
Detect 13, 18, 21, X and Y chromosomes numerical abnormality at one time by 27 STR markers.
■ Sensitive：
Only need 1ng DNA.
■ Easy-to-use:
Single-tube amplification, applicable for automatic and batched detection.
■ Fast:
Get results within 4 hours.
Workflow
Loci detected
Application
Prenatal diagnosis of 13, 18, 21, X and Y chromosome numerical abnormality
Sample types
Amniotic fluid, abortion tissue
Results
Instrument
Genetic analyzer (ABI PRISM 310, 3100 Genetic Analyzer, or ABI 3130 Series, 3500 Series, 3730 Series Genetic Analyzer)
※Reference :
Reprod Biomed Online. 2005 Dec;11(6):671-3.
※ For research use only