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ASPA Mouse Monoclonal Antibody [Clone ID: LBI4H4]

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]

Overview

ASPA mouse monoclonal antibody, clone LBI4H4

Synonyms

ACY2; ASP

Gene Name

Aspartoacylase

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

Concentration

1 mg/ml

Dilution

WB 1:2000

Form

PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Buffer

PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Function

Druggable Genome

Storage Conditions

Store 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

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/?term=443

Uniprot URL

https://www.uniprot.org/uniprot/P45381

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