ASPA Mouse Monoclonal Antibody [Clone ID: LBI3G7]

• 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:

  WB 1:2000

• 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 LBI3G7

• Gene ID URL:

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

• Uniprot URL:

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