Recombinant Human ASAH1 GST (N-Term) Protein

This product is produced by and distributed for Abnova, a company based in Taiwan.

This gene encodes a heterodimeric protein consisting of a nonglycosylated alpha subunit and a glycosylated beta subunit that is cleaved to the mature enzyme posttranslationally. The encoded protein catalyzes the synthesis and degradation of ceramide into sphingosine and fatty acid. Mutations in this gene have been associated with a lysosomal storage disorder known as Farber disease. Multiple transcript variants encoding several distinct isoforms have been identified for this gene. [provided by RefSeq]

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are guaranteed for 3 months from date of receipt.

Showing Publications 1 - 2 of 2.

Publications using H00000427-P01	Applications	Species
Huabin Z, John K, Chunwan L et al. Asah2 Represses the p53-Hmox1 Axis to Protect Myeloid-Derived Suppressor Cells from Ferroptosis. J Immunol. 2021-02-05 [PMID: 33547170]
Sabel MS, Liu Y, Griffith KA et al. Clinical Utility of Serum Autoantibodies Detected by Protein Microarray in Melanoma. Int J Proteomics. 2011-10-19 [PMID: 22084687]

Array H00000427-P01

• ASAH1 Antibodies
• ASAH1 ELISA Kit
• ASAH1 Lysate
• ASAH1 Proteins