PRENATAL GENETICS
Vysis MultiVysion PGT Multi-color Probe
For more information, contact Abbott.
For more information, contact Abbott.
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These fluorescence in situ hybridization (FISH) probes are intended to detect copy number of chromosomes 13, 18, 21, X, and Y.
The Vysis MultiVysion PGT Multi-color Probes consist of a 5-color, 5-probe mixture of DNA probe sequences homologous to specific regions on chromosomes 13, 18, 21, X, and Y. Each of the probes is directly labeled with 1 of the Vysis fluorophores. The probe mixture consists of:
Fluorophore-labeled human placental DNA (SpectrumBlue, SpectrumAqua, SpectrumOrange) is also included in the probe mixture to provide a nuclear stain that does not interfere with the probe fluorescent signal. Unlabeled blocking DNA is also included with the probe to suppress sequences contained within the target loci that are common to other chromosomes. The LSI 13 probe target is approximately 422 kb in length (chr13:47633474-48055374 February 2009 UCSC Human Genome Browser). The LSI 21 probe target is approximately 350 kb in length (chr21:39491467-39841748) February 2009 UCSC Human Genome Browser).
Normal Hybridization: MultiVysion PGT hybridized to an embryonic cell.
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Please be aware that the website you have requested is intended for the residents of a particular country or countries, as noted on that site. As a result, the site may contain information on pharmaceuticals, medical devices and other products or uses of those products that are not approved in other countries or regions.