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ASPA (4G3) Rabbit Monoclonal Antibody

ASPA (4G3) Rabbit Monoclonal Antibody

     
  • 1 - ASPA (4G3) Rabbit Monoclonal Antibody AP93725
    Western blot analysis of extracts from Human fetal kidney tissue using AP93725 at 1:1000.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC, IP
Primary Accession P45381, Q8R3P0, Q9R1T5
Reactivity Rat, Human, Mouse
Clonality Monoclonal
Calculated MW 35735 Da
Additional Information
Gene ID 443
Dilution WB~~1:1000
IHC~~1:100~500
IP~~N/A
Storage Conditions-20℃
Protein Information
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.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

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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