Clonit, società attiva nel campo della diagnostica molecolare con uno spiccato know-how nello sviluppo, produzione e distribuzione di reagenti innovativi per la diagnostica di malattie infettive e genetiche, a meno di tre mesi dall’ingresso di Equita Smart Capital ELTIF, fondo di private equity gestito da Equita Capital SGR, perfeziona l'acquisizione del 100% delle quote di Experteam, società che dal 1996 fornisce al mercato soluzioni personalizzate nel campo della diagnostica molecolare.

Experteam was founded in 1996 by molecular biologists Angelo De Bortoli & Federica Schiavon in Venice, Italy. Starting with a series of innovative molecular biology kits for detection of virus, protozoa, bacteria and for detection of carcinomas and genetic disorders.


The company now has an extensive range of reliable and robust molecular kits. Currently Experteam consists of a R&D and production department and a sales division. Experteam is committed to provide the market with customized solutions in the field of molecular diagnostics. 


Besides infertility, Experteam concentrates on oncology, genetic diseases, human virology and microbiology and environmental and food orientated microbiology and virology. The base of a wide range of products is the molecular detection using the Polymerase Chain Reaction (PCR) with either real- time PCR or gel or capillary electrophoresis. In addition to these techniques Experteam offer quantitative fluorescence PCR (QF-PCR) kits. 




distributors of "sistemas genomicos"
website "sistemas genomicos"
catalogue Experteam NGS Kits

old Website Experteam

BIOTECH PROJECT 1 (italian version - english version)

FESR 2007-2013 (download presentation)
Hypermutation kit1-FL (download Kit document)


Myotonic Distrophy

myotonicExperteam offers kits for the detection of DM1 and DM2 expanded alleles using "long range PCR", "TP-PCR", and Southern blotting as suggested by the guidelines "EMQN Best Practice Guidelines and Recommendations on Myotonic Dystrophy types 1 and 2".

Huntington’s disease

Huntington’s disease (HD) is a dominantly transmitted neurodegenerative disorder with wide variation in onset age but with an average age at onset of 40 years. HD is caused by the expansion of an unstable polymorphic tri-nucleotide (CAG)n repeat in exon 1 of the HTT gene (4p16.3). Repeats of 36 or larger are associated with disease expression, whereas repeats of 26 and smaller are normal. Intermediate numbers of repeats, could be associated with reduced penetrance whereby some develop HD and others do not.

PAI 1 coagulation Kit-RQ

Plasminogen activator inhibitor type 1 (PAI-1) is an important component of the coagulation system that down-regulates fibrinolysis in the circulation. Elevated circulating levels of PAI-1, have been related to the development of myocardial infarction.

There is evidence that a single nucleotide insertion/deletion (4G/5G) polymorphism in the promoter region of the PAI-1 gene is associated with circulating PAI-1 levels.