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MilliporeSigma™ anti-ARSA, Polyclonal

Mouse Polyclonal Antibody

Supplier:  MilliporeSigma™ AP113850UG

Catalog No. AP113850UG


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Description

Description

Specifically detects ARSA Clone: in Human samples, and it is validated for Immunohistochemistry (Paraffin)

ARSA hydrolyzes cerebroside sulfate. Defects in ARSA are known to cause metachromatic leukodystrophy (MLD). MLD is a disease due to a lysosomal storage defect. It is characterized by intralysosomal storage of cerebroside-3-sulfate in neural and non-neural tissues, with a diffuse loss of myelin in the central nervous system. Progressive demyelination causes a variety of neurological symptoms, including gait disturbances, ataxias, optical atrophy, dementia, seizures, and spastic tetraparesis. Three forms of the disease can be distinguished according to the age at onset: late-infantile, juvenile and adult.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

ARSA
Polyclonal
In PBS, pH 7.2.
Full length human ARSA (aa 1-507)
RUO
Recognizes the ∽55kDa ARSA protein in human lymph node tissue.
−20°C
IgG
Immunohistochemistry (Paraffin)
Unconjugated
Mouse
50 μg
Primary
Human
Purified
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