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MilliporeSigma™ Rabbit anti-AMACR, Polyclonal,
Rabbit Polyclonal Antibody
Supplier: MilliporeSigma™ ABC925
Description
Specifically detects AMACR in Human samples, and it is validated for Immunohistochemistry, Western Blotting
Alpha-methylacyl-CoA racemase is encoded by the AMACR gene and catalyzes the convertion of various (2R)-methylacyl-CoA esters to the corresponding (2S)-methylacyl-CoA epimers. AMACR deficiency (AMACRD) is a rare autosomal recessive peroxisomal disorder characterized by elevated plasma concentrations of pristanic acid C27-bile-acid intermediates, resulting in variable neurodegenerative symptoms affecting the central and peripheral nervous systems, including seizures, visual failure, sensorimotor neuropathy, spasticity, migraine, and white matter hyperintensities on brain imaging.
Specifications
AMACR | |
Polyclonal | |
Q9UHK6 | |
Rabbit | |
Affinity Purified | |
RUO | |
Primary | |
Human |
Immunohistochemistry, Western Blot | |
Purified rabbit polyclonal in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% sodium azide. | |
AMACR | |
GST-tagged recombinant protein corresponding to human AMACR near the N-terminal. | |
100 μg | |
Apoptosis, Cancer | |
NP_055139 | |
Stable for one year at 2°C to 8°C from date of receipt. |
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