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]

Overview

Carrier-free (BSA/glycerol-free) ASPA mouse monoclonal antibody, clone LBI1A11

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.