Polyclonal Antibodies
Anti-SMPD1 / ASM Polyclonal Antibody for WB, IF/ICC, ELISA - P17405
Item Number : CM0024324
Price varies based on specs and customizations
- Application
- WB, IF/ICC, ELISA
- Cross Reactivity
- Human, Mouse, Rat
- Protein Weight
- 70kDa
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Core Product Specifications and Parameters
| Parameter | Description |
|---|---|
| Product Name | SMPD1 / ASM Rabbit pAb |
| Remarks/Alias | ASM; NPD; ASMASE; SMPD1 / ASM |
| Species | Human |
| Gene ID (Human) | 6609 |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 70-340 of human SMPD1 / ASM (NP_000534.3) |
| Source | Rabbit |
| Category | Polyclonal Antibodies |
| Application | WB, IF/ICC, ELISA |
| Cross Reactivity | Human, Mouse, Rat |
| SWISS | P17405 |
| Protein Weight | 70kDa |
| Shipping | Ice bag |
Biological Background: SMPD1 / ASM Function and Localization
- SMPD1/ASM is a lysosomal hydrolase that converts sphingomyelin into ceramide, a lipid mediator involved in apoptosis, differentiation, and cell signaling. Related references: PMID:12563314, PMID:1840600, PMID:18815062
- It exists as two enzymatic forms: one targeted to the endolysosomal compartment and the other released extracellularly, with lysosomal exocytosis being a major source of the secretory form. Related references: PMID:20807762, PMID:21098024, PMID:9660788, PMID:12563314, PMID:20530211
- In lysosomes, it converts sphingomyelin to ceramide and plays a role in cholesterol export from intraendolysosomal membranes; it also has phospholipase C activity. Related references: PMID:20807762, PMID:21098024, PMID:25339683
- Secreted ASM reorganizes plasma membrane rafts by generating ceramide, which is crucial for host defense against pathogens like Pseudomonas aeruginosa. Related references: PMID:12563314, PMID:17303575, PMID:20807762, PMID:9393854
- Cleavage by CASP7 in the extracellular space yields a more active form that enhances ceramide production and plasma membrane repair during bacterial infection. Related references: PMID:21157428
- ASM activation is hijacked by viruses such as SARS-CoV and SARS-CoV-2 to facilitate infection, and by bacteria like N. gonorrhoeae.
- Genetic defects in SMPD1 lead to Niemann-Pick disease, a lysosomal storage disorder characterized by sphingomyelin accumulation.
Experimental Guidance and Technical Tips
- The immunogen covers a large central region (aa 70-340) of human SMPD1, suggesting the antibody may recognize both precursor and mature forms. Consider using protease inhibitors during sample preparation to maintain full-length protein integrity.
- For Western blot, a band around 70 kDa is expected. Verify specificity by using appropriate positive controls (e.g., human, mouse, or rat cell lysates known to express SMPD1) and include negative controls.
- In immunofluorescence/ICC, staining may be observed in lysosomal compartments; co-staining with lysosomal markers is recommended to confirm localization.
- The antibody cross-reacts with mouse and rat; therefore, it can be used in rodent model studies, but always validate in the relevant species and tissue context.
- ELISA protocols should be optimized with recombinant SMPD1 protein or appropriate coating antigens; consider pairing with matched detection antibodies for sandwich ELISA.
CamelBio: Your One-Stop Sourcing Bridge
CamelBio is your integrated sourcing partner for IVD raw materials, streamlining access to critical reagents like this anti-SMPD1/ASM antibody for research into sphingolipid metabolism, Niemann-Pick disease, and host-pathogen interactions. From validated antibody pairs and optimized polyclonal antibodies to bulk ancillary reagents and custom rare-target sourcing, we support your workflow from concept to clinic. Connect with our team to learn how we can fulfill your specific antibody and ancillary reagent requirements.
Product Datasheet
Anti-SMPD1 / ASM Polyclonal Antibody for WB, IF/ICC, ELISA - P17405
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