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linase

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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    TargetMol | Inhibitors_Agonists
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5-oxoprolinase/OPLAH Protein, Human, Recombinant (His & Myc)
Pyroglutamase, OPLAH, 5-oxoprolinase, 5-oxo-L-prolinase (5-OPase)
TMPH-00863
Expression system: E. coli
Length: 209-302, Partial
Activity: Not Tested
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20 days
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Buffer-exchangeable
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Acid sphingomyelinase/SMPD1 Protein, Human, Recombinant (His)
NPD, ASMASE, ASM
TMPY-01159
Acid sphingomyelinase SMPD1 Protein, Human, Recombinant (His) is expressed in Baculovirus-Insect Cells. The accession number is P17405-1.
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7-10 days
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Acid sphingomyelinase/SMPD1 Protein, Mouse, Recombinant (His)
Zn-SMase, sphingomyelin phosphodiesterase 1, A-SMase, aSMase, ASM
TMPY-02585
Sphingomyelin phosphodiesterase 1 (SMPD1) , also known as ASM ( acid sphingomyelinase ), is a member of the acid sphingomyelinase family of enzymes. Three isoforms have been identified, isoform 1 is 631 amino acids (aa) in length as the pro form, while Isoform 2 and isoform 3 have lost catalytic activity. The active SMPD1 isoform 1 contains one saposin B-type domain that likely interacts with sphingomyelin, and a catalytic region. Human SMPD1 is 86% aa identical to mouse SMPD1. SMPD1 is a monomeric lysosomal enzyme that converts sphingomyelin (a plasma membrane lipid ) into ceramide through the removal of phosphorylcholine. This generates second messenger components that participate in signal transduction. Defects in SMPD1 are the cause of Niemann-Pick disease type A (NPA) and type B (NPB), also known as Niemann-Pick disease classical infantile form and Niemann-Pick disease visceral form. Niemann-Pick disease is a clinically and genetically heterogeneous recessive disorder. NPB has little if any neurologic involvement and patients may survive into adulthood.
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7-10 days
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