ASPA Polyclonal Antibody (E-AB-14754)
For research use only.
Verified Samples |
Verified Samples in WB: Mouse brain Verified Samples in IHC: Human liver cancer, Human colon cancer |
Dilution | WB 1:1000-1:5000, IHC 1:50-1:200 |
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 | 0.5 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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Other Formats
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Unconjugated
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