Cell Biology Antibodies 6
Anti-SMPD1 / ASM Antibody (CAB16263)
- SKU:
- CAB16263
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Description
Antibody Name: | Anti-SMPD1 / ASM Antibody |
Antibody SKU: | CAB16263 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant protein of human SMPD1 / ASM |
Application: | WB IF |
Recommended Dilution: | WB 1:500 - 1:2000 IF 1:50 - 1:100 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | THP-1, HepG2, U-251MG, MCF-7, Mouse brain, Mouse liver, Rat brain, Rat liver |
Immunogen: | Recombinant protein of human SMPD1 / ASM |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | Email for sequence |
Gene ID: | 6609 |
Uniprot: | P17405 |
Cellular Location: | Lysosome |
Calculated MW: | 63kDa/64kDa/69kDa |
Observed MW: | 60kDa |
Synonyms: | SMPD1, ASM, ASMASE, NPD, SMPD1/ASM |
Background: | The protein encoded by this gene is a lysosomal acid sphingomyelinase that converts sphingomyelin to ceramide. The encoded protein also has phospholipase C activity. Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB). Multiple transcript variants encoding different isoforms have been identified. |
UniProt Protein Function: | SMPD1: Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity. Monomer. Belongs to the acid sphingomyelinase family. 3 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Phosphodiesterase; Lipid Metabolism - sphingolipid; EC 3.1.4.12 Chromosomal Location of Human Ortholog: 11p15.4-p15.1 Cellular Component: endosome; extracellular space; lysosomal lumen; lysosome; plasma membrane Molecular Function:protein binding; sphingomyelin phosphodiesterase activity; zinc ion binding Biological Process: ceramide biosynthetic process; glycosphingolipid metabolic process; negative regulation of MAP kinase activity; nervous system development; positive regulation of protein amino acid dephosphorylation; signal transduction; sphingomyelin catabolic process; sphingomyelin metabolic process Disease: Niemann-pick Disease, Type A; Niemann-pick Disease, Type B |
NCBI Summary: | The protein encoded by this gene is a lysosomal acid sphingomyelinase that converts sphingomyelin to ceramide. The encoded protein also has phospholipase C activity. Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB). Multiple transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2010] |
UniProt Code: | P17405 |
NCBI GenInfo Identifier: | 224471897 |
NCBI Gene ID: | 6609 |
NCBI Accession: | P17405.4 |
UniProt Secondary Accession: | P17405,P17406, Q13811, Q16837, Q16841, A8K8M3, E9PKS3 |
UniProt Related Accession: | P17405 |
Molecular Weight: | 69,624 Da |
NCBI Full Name: | Sphingomyelin phosphodiesterase |
NCBI Synonym Full Names: | sphingomyelin phosphodiesterase 1 |
NCBI Official Symbol: | SMPD1 |
NCBI Official Synonym Symbols: | ASM; NPD; ASMASE |
NCBI Protein Information: | sphingomyelin phosphodiesterase |
UniProt Protein Name: | Sphingomyelin phosphodiesterase |
UniProt Synonym Protein Names: | Acid sphingomyelinase; aSMase |
Protein Family: | Sphingomyelin phosphodiesterase |
UniProt Gene Name: | SMPD1 |
UniProt Entry Name: | ASM_HUMAN |
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