Human Karyomap-12 DNA Analysis Kit

A rapid PGT-M solution for single gene disorders

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Description: Kit contains BeadChips and reagents to perform the karyomapping assay sufficient for 24 samples.

Disclaimer: This product is labeled for Research Use Only - Not for use in diagnostic procedures.

What is PGT-M?

Preimplantation genetic testing for Monogenic Disease (PGT-M) relies on the use of genetic markers within the genome to assess the likelihood of an embryo carrying a gene mutation that may be linked to an inherited genetic disorder.

How PGT-M works?

1. If both parents carry a mutation for example for cystic fibrosis, there is a 1 in 4 chance that their offspring will have the disease.

2. Using knowledge of CF carrier or disease status in the parents, scientists can look at the chromosome segment in which the gene lies to determine from which parental chromosome the gene originated.

3. Scientists can then determine whether the chromosome segment inherited by each embryo contains the normal or mutated copy of the CF gene.

4. This helps determine whether the embryo inherited a single mutation from either parent and will be an unaffected carrier, whether the embryo inherited a mutation from each parent and will be affected with CF, or whether the embryo did not inherit any mutations. If the embryo is likely unaffected, it is considered to be a good candidate for transfer

Benefits of PGT-M

Enabling scientists to identify in vitro embryos that are likely to carry certain genetic disorders.

Advantages of PGT-M using Karyomapping

Faster results due to an ultra-rapid workflow compared to single tandem repeat (STR) technology¹

Minimal preparation - no disease - specific workup needed
Wide coverage - available for use with most single-gene conditions

1. Natesan S, Bladon AJ, Coskun S, et al. Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro. Genet Med. 2014;(January):1–8.