Enzyme and substrate measurements in the Gaucher disease mouse model 4L/PS-NA
QPS Neuropharmacology
QPS Austria is now able to offer Glucocerebrosidase (Gcase) activity as well as Glucosylceramide (GlcCer) and Glucosylsphingosine (GlcSph) measurements in your 4L/PS-NA study animals! These animals express the homozygous GbaV394L/V394L mutation (4L), have a complete prosaposin knockout (PS-) and a homozygous prosaposin transgene (NA) resulting in hypomorphic prosaposin levels. Measurement of GCase activity in brain …
Enzyme and substrate measurements in the Gaucher disease mouse model 4L/PS-NA
QPS Neuropharmacology
GBA1 deficiency and mutations are related to Gaucher disease, but are also shown to be linked to neurodegenerative events, e.g. in Parkinsons disease. QPS Austria offers the analysis of GCase activity in various in vitro and in vivo models like 1. mouse embryonic fibroblasts (MEFs) of 4L/PS-NA mice and 2. CBE treated D-Line mice, respectively. …