ASPA Polyclonal Antibody

• 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.

• Description:

  This is a ASPA Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• Synonyms:

  ACY 2, ACY-2, ACY2, ACY2, Aminoacylase 2, Aminoacylase-2, Aminoacylase2, ASP, ASPA, Aspartoacylase (aminoacylase 2, Canavan disease), Aspartoacylase (Canavan disease), Aspartoacylase, NUR 7, NUR7, OTTMUSP00000006437, RP23-213I10.1, Small lethargic

• Swiss Prot:

  P45381

• Accession Number:

  BC029128

• Reactivity:

  Human, Mouse, Rat

• Immunogen:

  Recombinant protein of human ASPA

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Polyclonal Antibody

• Applications:

  WB, IHC, ELISA

• Purification Method:

  Affinity purification

• Assay Type:

  Antibody

• Concentration:

  0.4 mg/mL

• Dilution:

  WB 1:1000-1:5000, IHC 1:100-1:300

• Buffer:

  PBS with 0.05% sodium azide and 50% glycerol, PH7.4

• Storage Conditions:

  Store at -20°C. Avoid freeze / thaw cycles.

• Calculated Molecular Weight:

  36 kDa

• Host or Source:

  Rabbit

• Isotype:

  IgG