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For research use only.

Verified Samples Verified Samples in WB: Mouse kidney, Human fetal kidney
Verified Samples in IHC: Human liver cancer, Human lymphoma
Dilution WB 1:1000-1:5000,  IHC 1:100-1:300
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC
Clonality Polyclonal
Immunogen Recombinant protein of human ASPA
Abbre ASPA
Synonyms ACY 2,  ACY-2,  ACY2,  ASP,  ASPA,  Aminoacylase 2,  Aminoacylase-2,  Aminoacylase2,  Aspartoacylase,  Aspartoacylase (Canavan disease),  Aspartoacylase (aminoacylase 2,  Canavan disease),  NUR 7,  NUR7,  OTTMUSP00000006437,  RP23-213I10.1,  Small lethargic
Swissprot
Calculated MW 36 kDa
Cellular Localization Cytoplasm. Nucleus.
Concentration 0.4 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Metabolism,  Neuroscience,  Signal Transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
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.
Other Clones

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Unconjugated

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