ASPA Mouse Monoclonal Antibody [Clone ID: LBI1A11]
Product Specifications
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]
Synonyms
ACY2; ASP
Gene Name
Homo sapiens aspartoacylase (ASPA), transcript variant 1, mRNA.
Gene ID
443
UniProt
P45381
Conjugation
Unconjugated
Related Pathways
Alanine, aspartate and glutamate metabolism, Histidine metabolism
Field of Research
Alanine, aspartate and glutamate metabolism, Histidine metabolism
Dilution
IHC 1:150
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Function
Druggable Genome
Storage Conditions
Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Symbol
ASPA
Overview
Carrier-free (BSA/glycerol-free) ASPA mouse monoclonal antibody, clone LBI1A11
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=443
Uniprot URL
https://www.uniprot.org/uniprot/P45381
Curated Selection
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