Preimplantation genetic testing is an investigative method used to detect chromosomal abnormalities and inherited diseases in an embryo before implantation in the uterus.
PG-Seq™ Rapid Kit v2
A kit for the detection of chromosomal abnormalities with a very concise protocol and the ability to use picogram quantities of input DNA. The kit is robust and can produce identical concentrations of DNA after whole genome amplification in different samples.
PG-Seq™ Rapid Non-Invasive Kit
Non-invasive genetic testing of DNA from blastocoel fluid or embryo culture media.
PG-Seq™ Kit 2.0
NGS solution for testing both aneuploidy and monogenic diseases. The kit includes DOPlify (used for whole-genome amplification of embryonic DNA), library preparation chemicals, and PG-Find software, which allows tracking of even small chromosomal aberrations.
Preimplantation genetic testing is an investigative method used to detect chromosomal abnormalities and inherited diseases in an embryo before implantation in the uterus.
PG-Seq™ Rapid Kit v2
A kit for the detection of chromosomal abnormalities with a very concise protocol and the ability to use picogram quantities of input DNA. The kit is robust and can produce identical concentrations of DNA after whole genome amplification in different samples.
PG-Seq™ Rapid Non-Invasive Kit
Non-invasive genetic testing of DNA from blastocoel fluid or embryo culture media.
PG-Seq™ Kit 2.0
NGS solution for testing both aneuploidy and monogenic diseases. The kit includes DOPlify (used for whole-genome amplification of embryonic DNA), library preparation chemicals, and PG-Find software, which allows tracking of even small chromosomal aberrations.