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|Tested species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Recombinant fragment corresponding to a region within amino acids 197 and 395 of ASAH1 (Uniprot ID#Q13510)|
|Purification||Antigen affinity chromatography|
|Storage buffer||0.1M tris glycine, pH 7, with 20% glycerol|
|Storage Conditions||-20° C, Avoid Freeze/Thaw Cycles|
|Tested Applications||Dilution *|
|Immunohistochemistry (Paraffin) (IHC (P))||1:100-1:1000|
|Western Blot (WB)||1:500-1:3000|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
PA5-34831 targets ASAH1 in IHC (P) and WB applications and shows reactivity with Human samples.
The PA5-34831 immunogen is recombinant fragment corresponding to a region within amino acids 197 and 395 of ASAH1 (Uniprot ID#Q13510).
Sphingolipids are hydrolyzed by ceramidases to yield sphingosine and fatty acids. These ceramidases are classified according to the pH range that supports their optimal activity. ASAH1 is an acid ceramidase and key regulator of ceramide metabolism. Mutations in this gene results in Farber Lipogranulomatosis, a fatal human genetic disorder that results in the painful swelling of the joints and tendons and pulminary insufficiency, while a complete knockout of its expression is lethal in mice. Recent studies have shown elevated levels of ASAH1 in Alzheimer"e;s disease (AD) patients correlating with a reduction in sphingomyelin and elevation of ceramide. Pretreatment of cultured neurons with recombinant AHAH1 prevented the cells from undergoing A-beta (Ab)-induced apoptosis. Multiple isoforms of this protein are known to exist.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
AC; ACDase; acid CDase; Acid ceramidase; Acylsphingosine deacylase; ASAH; N-acylsphingosine amidohydrolase; N-acylsphingosine amidohydrolase (acid ceramidase) 1; PHP; PHP32; Putative 32 kDa heart protein; SMAPME
AC; ACDase; ASAH; ASAH1; HSD-33; HSD33; PHP; PHP32; SMAPME