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MilliporeSigma™ anti-ARSA, Polyclonal
Mouse Polyclonal Antibody
Supplier: MilliporeSigma™ AP113850UG
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.
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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