ASPA Polyclonal Antibody | G-AB-00821

ASPA Polyclonal Antibody | G-AB-00821 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Cancer, Metabolism, Neuroscience, Signal Transduction

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: BC029128

Clonality: Polyclonal

Immunogen: Recombinant protein of human ASPA

Clone #:

Conjugation: Unconjugated

Swissprot: P45381

Santa Cruz: sc-109208/sc-109209/sc-109212/sc-98734

Calculated MW: 36 kDa

Observed MW:

Concentration: 0.4 mg/mL

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

Purification method: Affinity purification

Application: WB, IHC, ELISA

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

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

ASPA Polyclonal Antibody DataSheet