ASPA (4G3) Rabbit Monoclonal Antibody
ASPA (4G3) Rabbit Monoclonal Antibody
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- 实验流程
- 背景知识
Application ![]()
| WB, IHC, IP |
---|---|
Primary Accession | P45381, Q8R3P0, Q9R1T5 |
Reactivity | Rat, Human, Mouse |
Clonality | Monoclonal |
Calculated MW | 35735 Da |
Gene ID | 443 |
---|---|
Dilution | WB~~1:1000 IHC~~1:100~500 IP~~N/A |
Storage Conditions | -20℃ |
Name | ASPA (HGNC:756) |
---|---|
Function | 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 acts as a scavenger of NAA from body fluids. |
Cellular Location | Cytoplasm {ECO:0000250|UniProtKB:Q9R1T5}. Nucleus {ECO:0000250|UniProtKB:Q9R1T5} |
Tissue Location | Brain white matter, skeletal muscle, kidney, adrenal glands, lung and liver. |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
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. [provided by RefSeq, Jul 2008]

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