Aminoacylase 2 (ACY2) ELISA Kits

ACY2 encodes an enzyme that catalyzes the conversion of N-acetyl_L-aspartic acid (NAA) to aspartate and acetate.

list all ELISA KIts Gen GeneID UniProt
Anti-Human ACY2 ACY2 443 P45381
Anti-Maus ACY2 ACY2 11484 Q8R3P0
Anti-Ratte ACY2 ACY2 79251 Q9R1T5
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Weitere ELISA Kits für Aminoacylase 2 Interaktionspartner

Human Aminoacylase 2 (ACY2) Interaktionspartner

  1. report of 2 Egyptian sibling patients suspected of Canavan disease (CD); study revealed homozygosity for substitution T530C (Ile177Thr) in exon 4 of the ASPA (zeige ASPA ELISA Kits) gene in both sibs; substitution T530C (Ile177Thr) results in a novel missense mutation causing a CD phenotype with severe clinical characteristics

  2. Four ASPA (zeige ASPA ELISA Kits) missense mutations associated with Canavan disease are structurally characterized.

  3. Definitive evidence is presented to show that the recombinantly-expressed human aspartoacylase (zeige ASPA ELISA Kits) is not a glycoprotein.

  4. This is the first case report of ASPA (zeige ASPA ELISA Kits) mutation studies in Canavan disease from Indian subcontinent.

  5. a novel mutation Y88X within the aspartoacylase (zeige ASPA ELISA Kits) gene in a consanguineous family with an affected child diagnosed as Canavan disease.

  6. Human aspartoacylase (zeige ASPA ELISA Kits) gene expression was high not only in brain and kidney, but also in lung and liver.

  7. Gene ASPA (zeige ASPA ELISA Kits) (NM_000049) was undertaken to sequence for mutation analysis.

  8. We report on an Italian female patient with Canavan disease due to a missense mutation of the aspartoacylase (zeige ASPA ELISA Kits) gene and a 17p13.3 chromosomal microdeletion

  9. the ASPA (zeige ASPA ELISA Kits) gene was analysed in 22 unrelated non-Jewish patients with Canavan disease, and 24 different mutations were found

  10. Mild-onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase (zeige ASPA ELISA Kits) gene

Mouse (Murine) Aminoacylase 2 (ACY2) Interaktionspartner

  1. Gata6 (zeige GATA6 ELISA Kits) regulates differentiation, metabolism, and survival of resident peritoneal macrophages through aspartoacylase (zeige ASPA ELISA Kits).

  2. aspartoacylase (zeige ASPA ELISA Kits) is proposed here to support lipid synthesis and energy metabolism via the provision of substrate for both cellular processes during early postnatal development

  3. Intracellular vacuolisation in astrocytes coincides with axonal swellings in cerebellum and brain stem of aspa (zeige ASPA ELISA Kits)(lacZ/lacZ (zeige GLB1 ELISA Kits)) mutants indicating that astroglia may act as an osmolyte buffer in the aspa (zeige ASPA ELISA Kits)-deficient CNS

  4. Aspa (zeige ASPA ELISA Kits) defects were associated with increased levels of acetylated histone H3 (zeige HIST3H3 ELISA Kits), decreased chromatin compaction and increased GFAP (zeige GFAP ELISA Kits) protein, a marker for astrogliosis. Early in postnatal development ASPA (zeige ASPA ELISA Kits) defic affects oligodendrocyte maturation and myelination

  5. Death of OLs, neurons, and astrocytes was identified in every region of the aspartoacylase (zeige ASPA ELISA Kits) KO brain. These findings support involvement of ASPA (zeige ASPA ELISA Kits) in CNS development and function.

  6. ASPA (zeige ASPA ELISA Kits) gene defect in the mouse leads to spinal cord pathology; these changes may be involved in the cause of the physiological/behavioral abnormalities seen in the knockout mouse.

  7. normal hydrolysis of N-acetylaspartic acid is affected by aspartoacylase (zeige ASPA ELISA Kits) activity seen in the type 2 diabetes model mouse

  8. we now present immunoblot, proteomic, and biochemical evidence that the membrane-bound form of ASPA (zeige ASPA ELISA Kits) is intrinsic to purified myelin membranes.

  9. Nur7( Q193X) is a nonsense mutation in the mouse aspartoacylase (zeige ASPA ELISA Kits) gene that causes spongy degeneration of the CNS.

Aminoacylase 2 (ACY2) Antigen-Profil

Beschreibung des Gens

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.

Genbezeichner und Symbole assoziert mit Aminoacylase 2 (ACY2) ELISA Kits

  • aspartoacylase (ASPA) Antikörper
  • aspartoacylase (Aspa) Antikörper
  • aspartoacylase (aspa) Antikörper
  • ACY-2 Antikörper
  • Acy2 Antikörper
  • ASP Antikörper
  • nur7 Antikörper
  • zgc:171507 Antikörper

Bezeichner auf Proteinebene für Aminoacylase 2 (ACY2) ELISA Kits

ACY-2 , aminoacylase-2 , aspartoacylase (Canavan disease) , aminoacylase 2 , aspartoacylase (aminoacylase) 2 , Aminoacylase-2

100173374 Pongo abelii
443 Homo sapiens
11484 Mus musculus
79251 Rattus norvegicus
557232 Danio rerio
417609 Gallus gallus
611064 Canis lupus familiaris
100142661 Sus scrofa
509432 Bos taurus
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