Genetic disorder rapid diagnostic test AneuSure®
for medical researchtissuefor chromosomes

genetic disorder rapid diagnostic test
genetic disorder rapid diagnostic test
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Characteristics

Applications
for medical research, for genetic disorders
Sample type
tissue, amniotic fluid, for chromosomes
Analysis mode
QF-PCR

Description

For rapid detection of chromosomal aneuploidies for chromosomes 21, 18, 13, X and Y using QF-PCR technology. AneuSure Kit consists of 26 markers. The STR markers are distributed across autosomal chromosomes 21, 18 and 13 and sex chromosomes X & Y. The segmental duplication 7X marker is included in the kit for the differentiation of X chromosome monosomy from homozygosity (i.e. it quantifies the chromosome X for more accurate detection of Turner syndrome. AneuSure performance has been validated with extensive testing using Applied BiosystemsTM 3500/3500xL and 3130/3130xl platforms for detection and analysis on more than 1000 samples. Features Easy to use mix Multiplex analysis of 26 loci in one reaction ~ 90 min thermal clycling time Accurate detection of Turner syndrome Applicable to a variety of DNA sources – amniotic fluid (AF), chorionic villus (CVS), fetal tissue, etc.

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*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.