ASAH1 Antibody (PACO52354)
- SKU:
- PACO52354
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Application:
- IHC
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | ASAH1 Antibody (PACO52354) |
抗体コード: | PACO52354 |
サイズ: | 50ug |
宿主種: | Rabbit |
申し込み: | ELISA, WB, IHC |
推奨される希釈: | ELISA:1:2000-1:10000, WB:1:200-1:3000, IHC:1:20-1:200 |
反応性: | Human |
免疫原: | Recombinant Human acid, ceramidase protein (22-395AA) |
憲法: | Liquid |
ストレージバッファ: | Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 |
精製方法: | >95%, Protein G purified |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
![]() | Immunohistochemistry of paraffin-embedded human heart tissue using PACO52354 at dilution of 1:100. |
![]() | Western Blot. Positive WB detected in: Hela whole cell lysate. All lanes: ASAH1 antibody at 3µg/ml. Secondary. Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 45, 47 kDa. Observed band size: 45 kDa. |
バックグラウンド: | Hydrolyzes the sphingolipid ceramide into sphingosine and free fatty acid, |
シノニム: | acid, ceramidase (AC) (ACDase) (acid, CDase) (EC 3.5.1.23) (Acylsphingosine deacylase) (N-acylsphingosine amidohydrolase) (Putative 32 kDa heart protein) (PHP32) [Cleaved into: acid, ceramidase subunit alpha; acid, ceramidase subunit beta], ASAH1, ASAH |
UniProt Protein Function: | ASAH1: Hydrolyzes the sphingolipid ceramide into sphingosine and free fatty acid. Defects in ASAH1 are the cause of Farber lipogranulomatosis (FL); also known as Farber disease (FD). This sphingolipid disease is characterized by subcutaneous lipid-loaded nodules, excruciating pain in the joints and extremities, marked accumulation of ceramide in lysosomes, and death by three years of age. Defects in ASAH1 are the cause of spinal muscular atrophy with progressive myoclonic epilepsy (SMAPME). 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. Belongs to the acid ceramidase family. 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Lipid Metabolism - sphingolipid; EC 3.5.1.23; Hydrolase Chromosomal Location of Human Ortholog: 8p22 Cellular Component: lysosomal lumen Molecular Function:catalytic activity; ceramidase activity Biological Process: response to organic substance; sphingolipid metabolic process; glycosphingolipid metabolic process; ceramide metabolic process; lung development Disease: Farber Lipogranulomatosis |
NCBI Summary: | This gene encodes a heterodimeric protein consisting of a nonglycosylated alpha subunit and a glycosylated beta subunit that is cleaved to the mature enzyme posttranslationally. The encoded protein catalyzes the synthesis and degradation of ceramide into sphingosine and fatty acid. Mutations in this gene have been associated with a lysosomal storage disorder known as Farber disease. Multiple transcript variants encoding several distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008] |
UniProt Code: | Q13510 |
NCBI GenInfo Identifier: | 239938949 |
NCBI Gene ID: | 427 |
NCBI Accession: | Q13510.5 |
UniProt Secondary Accession: | Q13510,Q6W898, Q96AS2, E9PDS0, |
UniProt Related Accession: | Q13510 |
Molecular Weight: | 395 |
NCBI Full Name: | Acid ceramidase |
NCBI Synonym Full Names: | N-acylsphingosine amidohydrolase (acid ceramidase) 1 |
NCBI Official Symbol: | ASAH1 |
NCBI Official Synonym Symbols: | AC; PHP; ASAH; PHP32; ACDase; SMAPME |
NCBI Protein Information: | acid ceramidase; acid CDase; acylsphingosine deacylase; putative 32 kDa heart protein |
UniProt Protein Name: | Acid ceramidase |
UniProt Synonym Protein Names: | Acylsphingosine deacylase; N-acylsphingosine amidohydrolase; Putative 32 kDa heart protein; PHP32 |
Protein Family: | Acid ceramidase |
UniProt Gene Name: | ASAH1 |
UniProt Entry Name: | ASAH1_HUMAN |