Aspartoacylase (ASPA) Antibody

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Description
ASPA Antibody is a Rabbit Polyclonal antibody against ASPA. 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.
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Product specifications
Category | Primary Antibodies |
Immunogen Target | Aspartoacylase (ASPA) |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Recommended Dilution | IF/ICC: 1/50 - 1/100. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 60 µl |
Size 2 | 120 µl |
Size 3 | 200 µl |
Form | Liquid |
Tested Applications | IF/ICC |
Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P45381 |
Gene ID | 443 |
NCBI Accession | NP_001121557.1 |
Alias | ASPA,ACY2,ASP |
Background | Antibody anti-ASPA |
Status | RUO |
Note | Concentration: 1 mg/ml - |
Descripción
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Catalyzes the deacetylation of N-acetylaspartic acid(NAA) to produce acetate and L-aspartate. NAA occurs in high concentration in brain and its hydrolysis NAA plays a significant part in the maintenance of intact white matter. In other tissues it act as a scavenger of NAA from body fluids.
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Aspartoacylase (ASPA) Antibody
ASPA Antibody is a Rabbit Polyclonal antibody against ASPA. 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.
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