ACY2 rabbit pAb
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ACY2 rabbit pAb
Background:
This gene encodes an enzyme that catalyzes the conversion of N-acetyl_L-aspartic acid (NAA) to aspartate and acetate. NAA is abundant in the brain where hydrolysis by aspartoacylase is thought to help maintain white matter. This protein is an NAA scavenger in other tissues. Mutations in this gene cause Canavan disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]Description:
This gene encodes an enzyme that catalyzes the conversion of N-acetyl_L-aspartic acid (NAA) to aspartate and acetate. NAA is abundant in the brain where hydrolysis by aspartoacylase is thought to help maintain white matter. This protein is an NAA scavenger in other tissues. Mutations in this gene cause Canavan disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008],UniProt:
P45381Swiss Prot:
P45381Reactivity:
Human; Mouse; RatImmunogen:
Synthesized peptide derived from human ACY2 AA range: 67-117Clonality:
PolyclonalSource:
RabbitApplications:
WBConcentration:
1 mg/mlDilution:
WB 1: 500-2000Storage Conditions:
-20°C/1 yearFragment:
IgGSubcellular Location:
Cytoplasm. Nucleus .Gene ID (Human):
443
