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A13948

ASAH1 Rabbit polyclonal antibody

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£152.00

SKU:
A13948
Zusätzliche Namen:
AC|ACDase|ASAH|ASAH1|PHP|PHP32|SMAPME
Anwendung:
ELISA, WB, IF, ICC
Molekulargewicht:
40kda
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Abclonal
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulierung:
Unmodified
Sequenz:
IVAEDKKGHLIHGRNMDFGVFLGWNINNDTWVITEQLKPLTVNLDFQRNNKTVFKASSFAGYVGMLTGFKPGLFSLTLNERFSINGGYLGILEWILGKKDVMWIGFLTRTVLENSTSYEEAKNLLTKTKILAPAYFILGGNQSGEGCVITRDRKESLDVYELDAKQGRWYVVQTNYDRWKHPFFLDDRRTPAKMCLNRTSQENISFETMYDVLSTKPVLNKLTVYTTLIDVTKGQFETYLRDCPDPCIGW
Uniprot:
Q13510
Synonyme:
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
Weitere 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.
Versandbedingungen:
Blue Ice