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Neonatal Screening

Fast and easy detection

Newborn screening allows detection shortly after birth of treatable conditions. Genetic diseases that need to be detected as soon as possible in infants can also be tested by newborn screening. Our technique allows for rapid detection of treatable genetic errors, directly from dried blood spots and without the need of DNA extraction.

KITS

SMA (SMN1 & 840C>T)

SCID (TREC & KREC)

LACAR's kits improve the efficiency of the process

Reliable genotyping

SIMPLICITY

No laborious DNA extraction procedure

RAPIDITY

1 minute hand-time
25 minutes amplification + detection

EFFICIENCY

Perfect distinction of the heterozygote

3 DIFFERENT SOLUTIONS TO FIT WITH ALL LABS' VOLUMES

LC-GENIE III

Get started with your genetic portfolio or outsource low-medium throughput from busy qPCR platforms with a fully CE-IVD solution from the primary tube to the end results

qPCR PLATFORMS

CE-IVD solution from the primary tube to the end results available on many already established qPCR platforms

AUTOMATISATION

Unique CE-IVD fully automated system from the primary tube to the end results at a reasonable price

Want to know more about Neonatal Screening?

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