SMPD1 anticorps (AA 204-558)
Aperçu rapide pour SMPD1 anticorps (AA 204-558) (ABIN7872093)
Antigène
Voir toutes SMPD1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 204-558
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Fonction
- aSMase Antibody / Smpd1 / Acid sphingomyelinase
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Purification
- Antigen affinity purified
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Immunogène
- Recombinant mouse protein (amino acids D204-M558) was used as the immunogen for the aSMase antibody.
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Isotype
- IgG
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Indications d'application
- Optimal dilution of the aSMase antibody should be determined by the researcher.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Buffer
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- After reconstitution, the aSMase antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- SMPD1 (Sphingomyelin phosphodiesterase 1, Acid Lysosomal (SMPD1))
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Autre désignation
- aSMase
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Sujet
- Sphingomyelin phosphodiesterase 1 (SMPD1), also known as acid sphingomyelinase (ASM or aSMase), is an enzyme that in humans is encoded by the SMPD1 gene. Enables acid sphingomyelin phosphodiesterase activity and zinc ion binding activity. Involved in ceramide biosynthetic process, positive regulation of apoptotic process, and response to ionizing radiation. Acts upstream of or within ceramide metabolic process, cholesterol metabolic process, and sphingomyelin catabolic process. Located in extracellular space. Is expressed in several structures, including alimentary system, integumental system, nervous system, sensory organ, and skeleton. Used to study Niemann-Pick disease. Human ortholog(s) of this gene implicated in Niemann-Pick disease, Niemann-Pick disease type A, and Niemann-Pick disease type B. Orthologous to human SMPD1 (sphingomyelin phosphodiesterase 1).
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UniProt
- Q04519
Antigène
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