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innovative DNA Screening solutions
Microdeletion syndromes are disorders brought about by the deletion of specific regions of chromosomal DNA causing haploinsufficiencies of a variable number of important genes. These deletions are difficult to visualise using standard cytogenetic techniques but Fluorescence In Situ Hybridisation (FISH) can resolve these submicroscopic deletions and has therefore become the method of choice for the diagnosis of these disorders.
Cytocell's comprehensive range of Microdeletion probes features products for some of the rarest human genetic syndromes. With this in mind, we offer all Microdeletion probes in economical five or standard ten test kits. Within this range Cytocell offer 10 unique probes, 5 of which are combination probes where you get two probes for the price of one.
myProbes™ is a custom FISH probe design and manufacture service that utilises Cytocell's proprietary BAC clone collection. If a product you require does not appear in the catalogue, do not hesitate to contact Cytocell with your request.
5 and 10 tests
Supplied with DAPI counterstain and full instructions for use.
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