Genetic disorder test kit

for DNAwhole bloodfor chromosomes

Y Chromosome DNA Microdeletions qPCR Detection Ki Ychromosome microdeletion is a disease lead by gene problem. It will affectsperm production when azoospermia exists on the Y chromosome. However, the genelocus is too small to be detected by the conventional methods. This kit canbe used for the diagnosis of Y-chromosomal microdeletionsof the AZFa (sY84 and sY86), AZFb (sY127 and sY134), and AZFc (sY254 and sY255)region on azoospermic and oligozoospermic men. 32 Reactions/Kit Applicable Instrument ABI 7500 Real-Time PCR System Samples Human EDTA anticoagulant whole blood, human sodium citrateanticoagulant whole blood, or human oral exfoliated cell. Pathogens Assay for the detection of Y chromosome microdeletion Methods Multiplex qPCR method, Taqman fluorescent probe technology Detection Y-chromosomal microdeletions of the AZFa (sY84 and sY85), AZFb (sY127 and sY134) and AZFc (sY254 and sY255) Indications ICSi therapy auxiliary diagnosis male patients with oligospermia and azoospermia Male infectility with normal sperm density Male infertility with cryptorchidism and varicocele Unexplained habitual abortion of patients' wife sperm library screening Assay Two PCR reaction solutions Results Automatic data reports Efficiency Real-time High-accuracy Indexes Coincidence rate:100% Variation coefficient: less than 5% No cross reactions