Custom products not listed in our catalog can also be provided. Please contact us with your needs.
If you are interested in any of our future products listed below, please send us an email, and we can keep you posted about expected availability dates.
Glycosaminoglycan fragments (internal and non-reducing end, deuterated and non-deuterated) for analysis of deficiency of glycosaminoglycan-degrading enzymes.
Kubaski, F., Suzuki, Y., Orii, K., Giugliani, R., Church, H.J., Mason, R.W., Dũng, V.C., Ngoc, C.T.B., Yamaguchi, S., Kobayashi, H. and Girisha, K.M., 2017. Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses. Molecular genetics and metabolism, 120(3), pp.247-254.
Saville, J.T., McDermott, B.K., Fletcher, J.M. and Fuller, M., 2018. Disease and subtype specific signatures enable precise diagnosis of the mucopolysaccharidoses. Genetics in Medicine, p.1.
Lawrence, R., Brown, J.R., Al-Mafraji, K., Lamanna, W.C., Beitel, J.R., Boons, G.J., Esko, J.D. and Crawford, B.E., 2012. Disease-specific non–reducing end carbohydrate biomarkers for mucopolysaccharidoses. Nature chemical biology, 8(2), p.197.
Bile acid B for analysis of NPC1 and NPC2 (deuterated and non-deuterated)
Jiang, X., Sidhu, R., Mydock-McGrane, L., Hsu, F.F., Covey, D.F., Scherrer, D.E., Earley, B., Gale, S.E., Farhat, N.Y., Porter, F.D. and Dietzen, D.J., 2016. Development of a bile acid–based newborn screen for Niemann-Pick disease type C. Science translational medicine, 8(337), pp.337ra63-337ra63.
Bile tetrol-glucuronide (deuterated and non-deuterated) for analysis of CYP27A1
Vaz, F.M., Bootsma, A.H., Kulik, W., Verrips, A., Wevers, R.A., Schielen, P.C., DeBarber, A.E. and Huidekoper, H.H., 2017. A newborn screening method for cerebrotendinous xanthomatosis using bile alcohol glucuronides and metabolite ratios. Journal of lipid research, pp.jlr-P075051.
Various bile biosynthetic intermediates (deuterated and non-deuterated) for analysis of bile acid biosynthesis
Heubi, J.E., Setchell, K.D. and Bove, K.E., 2018. Inborn Errors of Bile Acid Metabolism. Clinics in liver disease, 22(4), pp.671-687.