硕肯生物硕肯生物Soken.bio
查看试用产品 →开放浏览 · 登录后申请
抗人 ASAH2 抗体对
试剂盒

抗人 ASAH2 抗体对

01AB00645

Neutral ceramidase (ASAH2), encoded by the ASAH2 gene, is a type II integral membrane protein that plays a vital role in sphingolipid metabolism by hydrolyzing ceramide into sphingosine and free fatty acids. This enzymatic activity is crucial for regulating cellular levels of bioactive sphingolipids, which are involved in various signaling pathways related to cell growth and apoptosis. The protein exhibits optimal activity at a neutral pH (6.5-8.5) and is expressed predominantly in the brush border membranes of the intestine, as well as in other tissues like the kidney and brain. Dysregulation of ASAH2 has been implicated in several diseases, particularly in cancer; for instance, its inhibition has been linked to delayed tumor growth and increased ceramide levels in xenograft models. Additionally, ASAH2 is essential for the digestion of dietary sphingolipids in the intestine, and its deficiency can lead to impaired intestinal ceramide degradation, potentially affecting overall intestinal health and disease susceptibility.

Human
规格起售价
登录后可查看

技术参数

靶点基因名
ASAH2
基因别名
HNAC1
蛋白别名
N-acylsphingosine amidohydrolase 2; ASAH2
UniProt
Q9NR71
物种
Human

产品详情

靶点名称
ASAH2
蛋白名称
N-acylsphingosine amidohydrolase 2
蛋白别名
Neutral ceramidase; N-CDase; NCDase; Acylsphingosine deacylase 2; BCDase; LCDase; hCD; N-acylsphingosine amidohydrolase 2; Non-lysosomal ceramidase) [Cleaved into: Neutral ceramidase soluble form]
靶点基因名
ASAH2
基因别名
HNAC1
UniProt
Q9NR71
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Neutral ceramidase (ASAH2), encoded by the ASAH2 gene, is a type II integral membrane protein that plays a vital role in sphingolipid metabolism by hydrolyzing ceramide into sphingosine and free fatty acids. This enzymatic activity is crucial for regulating cellular levels of bioactive sphingolipids, which are involved in various signaling pathways related to cell growth and apoptosis. The protein exhibits optimal activity at a neutral pH (6.5-8.5) and is expressed predominantly in the brush border membranes of the intestine, as well as in other tissues like the kidney and brain. Dysregulation of ASAH2 has been implicated in several diseases, particularly in cancer; for instance, its inhibition has been linked to delayed tumor growth and increased ceramide levels in xenograft models. Additionally, ASAH2 is essential for the digestion of dietary sphingolipids in the intestine, and its deficiency can lead to impaired intestinal ceramide degradation, potentially affecting overall intestinal health and disease susceptibility.