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A13948

ASAH1 Rabbit polyclonal antibody

Size

£152.00

SKU:
A13948
Additional Names:
AC|ACDase|ASAH|ASAH1|PHP|PHP32|SMAPME
Application:
ELISA, WB, IF, ICC
Molecular Weight:
40kda
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Abclonal
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulation:
Unmodified
Sequence:
IVAEDKKGHLIHGRNMDFGVFLGWNINNDTWVITEQLKPLTVNLDFQRNNKTVFKASSFAGYVGMLTGFKPGLFSLTLNERFSINGGYLGILEWILGKKDVMWIGFLTRTVLENSTSYEEAKNLLTKTKILAPAYFILGGNQSGEGCVITRDRKESLDVYELDAKQGRWYVVQTNYDRWKHPFFLDDRRTPAKMCLNRTSQENISFETMYDVLSTKPVLNKLTVYTTLIDVTKGQFETYLRDCPDPCIGW
Uniprot:
Q13510
Synonyms:
AC;ACDase;acid CDase;acid ceramidase;acylsphingosine deacylase;ASAH;N-acylethanolamine hydrolase ASAH1;N-acylsphingosine amidohydrolase;N-acylsphingosine amidohydrolase (acid ceramidase) 1;PHP;PHP32;putative 32 kDa heart protein;SMAPME
Extra Details:
This gene encodes a member of the acid ceramidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. Processing of this preproprotein generates alpha and beta subunits that heterodimerize to form the mature lysosomal enzyme, which catalyzes the degradation of ceramide into sphingosine and free fatty acid. This enzyme is overexpressed in multiple human cancers and may play a role in cancer progression. Mutations in this gene are associated with the lysosomal storage disorder, Farber lipogranulomatosis, and a neuromuscular disorder, spinal muscular atrophy with progressive myoclonic epilepsy.
Shipping Conditions:
Blue Ice