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Human Sphingomyelin Phosphodiesterase ELISA Kit

Human Sphingomyelin Phosphodiesterase ELISA Kit

SKU:IHUSMPD1KT

Regular price $744.00
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This Human Sphingomyelin Phosphodiesterase ELISA Kit from Innovative Research is intended for quantitative detection of human SMPD1 in cell culture supernates, serum and plasma (heparin). Strip well format. Reagents for up to 96 tests.

This human SMPD1 ELISA Kit is based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for SMPD1 has been precoated onto 96-well plates. Standards(Expression system for standard: CHO, Immunogen sequence: L47-C631) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for SMPD1 is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex is added and unbound conjugates are washed away with PBS or TBS buffer. HRP substrate TMB are used to visualize HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the human SMPD1 amount of sample captured in plate.

  • Detection Target: Sphingomyelin Phosphodiesterase
  • Uniprot ID: P17405)
  • Reactivity: Human
  • Cross-Reactivity: There is no detectable cross-reactivity with other relevant proteins.
  • Range: 15.6pg/ml-1000pg/ml
  • Sensitivity: <10pg/ml
  • Storage Conditions: Store at 4?C for 6 months, at -20?C for 12 months. Avoid multiple freeze-thaw cycles. (Shipped with wet ice)



Additional Information:

The capture antibody is a monoclonal antibody from mouse, the detection antibody is a biotinylated polyclonal antibody from goat. Expression system for standard: Sphingomyelin phosphodiesterase 1 (SMPD1), also known as acid sphingomyelinase (ASM), is an enzyme that in humans is encoded by the SMPD1 gene. This gene is mapped to 11p15.4. 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. Sphingomyelin phosphodiesterase 1 belongs to the sphingomyelin phosphodiesterase family.; Immunogen sequence: 369

This material is sold for in-vitro use only for manufacturing and research. This material is not suitable for human or animal use. While we make every effort to ensure the safety of our products, we recommend handling any biological materials with standard precautions as if capable of spreading infectious disease. The statements herin are offered for informational purposes only to be used solely for your consideration, investigation, and verification.

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