Acid Sphingomyelinase Rabbit Polyclonal Antibody

CAT#: AP05201PU-N

Acid Sphingomyelinase rabbit polyclonal antibody, Purified



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CNY 10260.00


货期*
4周

规格
    • 100 ug

Product images

Specifications

Product Data
Applications ELISA, WB
Recommend Dilution Western blot (5-10 µg/ml).
ELISA.
Reactivity Human
Host Rabbit
Clonality Polyclonal
Immunogen Synthetic peptide derived from human acid sphingomyelinase protein.
Specificity The antibody recognizes human acid sphingomyelinase.
Formulation PBS, pH 7.4 containing 0.08% Sodium Azide as preservative.
State: Purified
State: Liquid purified IgG fraction.
Concentration lot specific
Conjugation Unconjugated
Storage Condition Ship at ambient temperature, freeze upon arrival.
Product should be stored (in aliquots) at -20°C.
Avoid repeated freezing and thawing.
Background Human acid sphingomyelinase (sphingomyelin phosphodiesterase, ASM) is the lysosomal enzyme responsible for the hydrolysis of sphingomyelin to ceramide and phosphocholine. Converts sphingomyelin to ceramide. aSM also has phospholipase C activities toward 1,2-diacylglycerol-phosphocholine and 1,2-diacylglycerol-phosphoglycerol. The enzyme is a membrane-associated glycoprotein with a pH optimum of about 4.5 and a subunit molecular mass of about 72 kDa. In addition AtoS M, two other sphingomyelinases have been identified in man, a Mg2+- dependent neutral sphingomyelinase found primarily in brain and a Zn2+-dependent acid sphingomyelinase found primarily in serum. Although it is likely that the acid and neutral sphingomyelinases are coded by different genes, the molecular genetic relationship of these three biochemically distinct sphingomyelinases has not been determined. Understanding the role of these sphingomyelinases in the hydrolysis of sphingomyelin to ceramide will be an important step in the understanding of ceramide as it is further hydrolyzed to sphingosine, a neutral phospholipid which has been implicated in the regulation of protein kinase C-mediated signal transduction. Inherited deficiencies of ASM have been reported in man, deficient ASM activity results in the two major subtypes of Niemann-Pick disease (NPD).
Synonyms Acid Sphingomyelinase, aSMase, SMPD1, ASM, Sphingomyelin Phosphodiesterase, ASM-1
Reference Data
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
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