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The NeoLSD MSMS Kit is intended for the quantitative measurement of the activity of the enzymes acid-β-glucocerebrosidase (ABG), acid-sphingomyelinase (ASM), acid α glucosidase (GAA), β galactocerebrosidase (GALC), α-galactosidase A (GLA) and α-L-iduronidase (IDUA) in dried blood spots (DBS) from newborn babies.

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The first commercial IVD kit for newborn screening of Pompe, MPS-I, Fabry, Gaucher, Niemann-Pick A/B and Krabbe disorders from a single DBS sample.

Due to advancements in treatments of lysosomal storage disorders and the subsequently increasing demand for newborn screening of these disorders, we are proud to release the NeoLSD MSMS Kit, the first commercial mass spectrometry based IVD kit for newborn screening of up to six lysosomal storage disorders from a single blood spot punch. The analysis of the enzymatic activity is intended as an aid in screening newborns for the following lysosomal storage disorders respectively; Gaucher Disease, Niemann-Pick A/B Disease, Pompe Disease, Krabbe Disease, Fabry Disease, and MPS I Disease.

The NeoLSD MSMS kit enables running up to 500 tests per instrument per day and easily switching between NeoBase 2 and NeoLSD kits on a single MSMS instrument. In addition, the NeoLSD kit provides you a wide analytical range, leading to potentially lower false positive rates, less costs associated with repeat enzyme activity tests and molecular testing.

The Benefits of the assay are as below:

  • Screen for up to six LSDs from a single DBS punch and single incubation thereby saving time, human resources and consumables
  • Provides wide dynamic range enabling better separation of affected and non-affected individuals
  • High sample volume per day to meet the rising demand of newborn screening

The kit includes all necessary for effective LSD newborn screen. It comes equipped with 3 packages.


Newborn Screening
Detection Method
Mass Spectrometry (MSMS)
Niemann-Pick A/B
Technology Type
Unit Size
1 Kit

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