Biovision
Human CellExp™ Acid Sphingomyelinase, Human Recombinant
- SKU:
- 26-P1443
- Availability:
- Usually Shipped in 5 Working Days
- Storage Temperature:
- -20°C
- Shipping Conditions:
- Gel Pack
- Shelf Life:
- 12 months
Description
Biomolecule/Target: N/A
Synonyms: Sphingomyelin phosphodiesterase, aSMase, acid sphingomyelinase, SMPD1, ASM, EC:3.1.4.12
Alternates names: Sphingomyelin phosphodiesterase, aSMase, acid sphingomyelinase, SMPD1, ASM, EC:3.1.4.12
Taglines: Catalyzes the hydrolysis of sphingomyelin to ceramide and phosphorylcholine
Taglines: USA
Country of Animal Origin: USA
NCBI Gene ID #.: 6609
NCBI Gene Symbol: SMPD1
Gene Source: Human
Accession #: P17405
Recombinant: True
Source: HEK 293 cells
Purity by SDS-PAGE #: > 95%
Assay: SDS-PAGE.
Purity: N/A
Assay #2: N/A
Endotoxin Level: N/A
Activity (Specifications/test method): The specific activity is >2 U/mg. Measured by its ability to cleave 2-N-Hexadecanoylamino-4-nitrophenylphosphorylcholine (HNPPC, freshly dissolved in DMSO) which can be detected at 420 nm.
Biological activity: The specific activity is >2 U/mg. Measured by its ability to cleave 2-N-Hexadecanoylamino-4-nitrophenylphosphorylcholine (HNPPC, freshly dissolved in DMSO) which can be detected at 420 nm.
Results: N/A
Binding Capacity: N/A
Unit Definition: One unit of aSMase/ASM is defined as the amount of enzyme that hydrolyzes 1.0 µmol of substrate HNPPC per min under the assay conditions at 37 ºC.
Molecular Weight: 68 kDa (C-terminal 8×His tag)
Concentration: N/A
Appearance: Lyophilized powder
Physical form description: Lyophilized
Reconstitution Instructions: Centrifuge the vial prior to opening. Reconstitute in distilled water. Do not vortex.
Background Information: Sphingomyelin phosphodiesterase, which is encoded by the SMPD1 gene, is also known as acid sphingomyelinase or aSMase. There are two types of sphingomyelinases: ASM (acid), and NSM (neutral). ASM / aSMase can catalyze the hydrolysis of sphingomyelin to ceramide and phosphorylcholine with cofactor Zn2+. Ceramide, a bioactive lipid, has emerged as an important signaling molecule involved in a variety of cellular processes such as cell differentiation, apoptosis, and proliferation. Mutations in the SMPD1 gene cause Niemann–Pick disease types A and B due to deficiency in hydrolyzing sphingomyelin to ceramide. Activation of ASM can be achieved by the removal of its C terminal cysteine residue or C-terminal truncation. BioVision’s recombinant human ASM was expressed from HEK293 cells without the last three C terminal residues, and is therefore constitutively active.
Amino acid sequence: His 62 - Pro 628
Handling: Centrifuge the vial prior to opening.
Usage: N/A