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Rabbit Anti-ASAH1 Antibody (CSB-PA619774ESR2HU)
Supplier: CUSABIO BIOTECH CO.
AC Antibody,ACDase Antibody,Acid CDase Antibody,Acylsphingosine deacylase Antibody,N-acylsphingosine amidohydrolase Antibody,Putative 32 kDa heart protein Antibody,PHP32 Antibody,ASAH1 Antibody,ASAH Antibody,HSD-33 Antibody, HSD33 AntibodyMore alternative names for the antibody
AC antibody|ACDase antibody|Acid CDase antibody|Acid ceramidase antibody|Acid ceramidase precursor antibody|Acid ceramidase subunit beta antibody|Acylsphingosine deacylase antibody|ASAH 1 antibody|ASAH antibody|ASAH1 antibody|ASAH1_HUMAN antibody|FLJ21558 antibody|FLJ22079 antibody|N acylsphingosine amidohydrolase (acid ceramidase) 1 antibody|N acylsphingosine amidohydrolase 1 antibody|N acylsphingosine amidohydrolase antibody|N-acylsphingosine amidohydrolase antibody|N-acylsphingosine deacylase antibody|PHP antibody|PHP32 antibody|Putative 32 kDa heart protein antibody|SMAPME antibody
Anti-ASAH1 antibody (ab74469)
Anti-ASAH1 antibody (ab74469)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Acid ceramidase protein (146-395AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:427( Human), Entrez Gene:11886( Mouse), Entrez Gene:84431( Rat), Omim:613468( Human), SwissProt:Q13510( Human), SwissProt:Q9WV54( Mouse), SwissProt:Q6P7S1( Rat), Unigene:527412( Human), Unigene:22547( Mouse), Unigene:127798( Rat)
|Protein function|| |
Hydrolyzes the sphingolipid ceramide into sphingosine and free fatty acid.
|Protein tissue specificity|| |
Broadly expressed with highest expression in heart.
|Involvement in disease|| |
Farber lipogranulomatosis (FRBRL) [MIM:228000]: An autosomal recessive lysosomal storage disorder characterized by subcutaneous lipid-loaded nodules, excruciating pain in the joints and extremities, and marked accumulation of ceramide in lysosomes. Disease severity is variable. The most severe disease subtype is a rare neonatal form with death occurring before 1 year of age. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Spinal muscular atrophy with progressive myoclonic epilepsy (SMAPME) [MIM:159950]: An autosomal recessive neuromuscular disorder characterized by childhood onset of motor deficits and progressive myoclonic seizures, after normal developmental milestones. Proximal muscle weakness and generalized muscular atrophy are due to degeneration of spinal motor neurons. Myoclonic epilepsy is generally resistant to conventional therapy. The disease course is progressive and leads to respiratory muscle involvement and severe handicap or early death from respiratory insufficiency. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the acid ceramidase family.
|Protein cellular localization|| |
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CUSABIO BIOTECH CO.
|Product type|| |
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