The HumanKaryomap-12 DNA Analysis Kit provides a comprehensive test for preimplantation genetic diagnosis (PGD) of single-gene defects using a single cell or a few cells, from an embryo. PGD with karyomapping enables screening of embryos for the likelihood of carrying the defective gene prior to implantation. Karyomapping uses SNP (single nucleotide polymorphisms) array technology to confirm the presence or absence of a specific allele. It consists of microarray analysis using the HumanKaryomap-12 DNA Analysis Kit, scanning on the iScan or NextSeq 550 system, and analysis and reporting using BlueFuse Multi software.
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Specifications | |||
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Number of Fixed Markers | 264,909 | Assay | Infinium Karyomapping |
Number of Samples | 12 | Instrument Support | HiScan or iScan or NextSeq 550 |
Genomic DNA Requirement | 8 ul SureMDA WGA Product | Scan Time/Sample | 5 min |
WGA DNA Requirement | 400 ng at 50ng/ul | Spacing (kb) | 1 marker/5.5kb |
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