Designed for rapid and cost-effective deletion analysis of the SMN1 gene (Exons 7 and 8).
Ensures accurate results using TaqMan probe-based CNV analysis and the comparative Ct method.
Offers automated data analysis on the Bio-Rad CFX96 instrument.
The geneMAP™ SMN1 Exon 7/8 Deletion Screening Kit is an in vitro nucleic acid amplification test designed to assist in the screening of spinal muscular atrophy (SMA) carriers and the diagnosis of SMA. SMA is a severe central nervous system disorder and a leading genetic cause of infant mortality. Most carriers possess only one copy of the SMN1 gene. Approxi- mately 94% of SMA patients lack both copies of SMN1 Exons 7 and 8, which can be detected using standard molecular analyses. Due to the high carrier frequency in the population, carrier testing for SMA plays a crucial role in genetic counse- ling.
CAT NO. : SMN1M-RT50 / SMN1M-RT500
PRODUCT : geneMAP™ SMN1 Exon 7/8 Deletion Screening Kit
SIZE : 50 / 500 TEST
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