Alanyl-tRNA Synthetase 2, Mitochondrial (Putative) (AARS2) ELISA Kits

The protein encoded by AARS2 belongs to the class-II aminoacyl-tRNA synthetase family. Additionally we are shipping AARS2 Antibodies (63) and AARS2 Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
AARS2 57505 Q5JTZ9
Anti-Rat AARS2 AARS2 301254 D3ZX08
Anti-Mouse AARS2 AARS2 224805 Q14CH7
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Catalog No. Reactivity Sensitivity Range Images Quantity Delivery Price Details
  96 Tests 13 to 16 Days

More ELISA Kits for AARS2 Interaction Partners

Human Alanyl-tRNA Synthetase 2, Mitochondrial (Putative) (AARS2) interaction partners

  1. clinical, biochemical and molecular investigations of two unrelated boys presenting with fatal infantile cardiomyopathy, lactic acidosis and respiratory failure

  2. AARS2-related leukoencephalopathy is a new variant of mitochondrial encephalomyopathy.

  3. Two AARS2 variants, (c.2872C > T) and (c.1774C > T), were identified in a child with cardiomyopathy with early-onset brain disease.

  4. Three patients with ovarioleukodystrophy, carrying AARS2 compound heterozygous mutations have been found.

  5. Missense variants in the AARS2 gene are the likely cause of the retinopathy and optic atrophy in this patient. This finding expands the phenotypic spectrum of the AARS2 gene.

  6. Mutations in AARS2 in a Series of CSF1R-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia.

  7. This paper documented a new, nonsense AARS2 gene mutation (c.578T>G, p.Leu193*) and a known missense mutation (c.595C>T, p.Arg199Cys) associated with leukoencephalopathy in a male patient.

  8. we describe a Japanese woman with novel compound heterozygous mutations in AARS2, the first report of leukodystrophy caused by AARS2 mutations in Asia.

  9. A new phenotype caused by AARS2 mutations is characterized by leukoencephalopathy and ovarian failure in female patients, indicating that the phenotypic spectrum associated with AARS2 variants is much wider than previously reported.

  10. Mutations in AARS2 found in lethal mitochondrial myopathy

Mouse (Murine) Alanyl-tRNA Synthetase 2, Mitochondrial (Putative) (AARS2) interaction partners

  1. Editing-deficient mitochondrial alanyl-tRNA synthetase (mtAlaRS) mice, bearing either a mild or a severe mtAlaRS editing mutation, and indicate that editing of mischarged tRNAs by alanyl-tRNA synthetase is an essential protein quality control mechanism in mammalian mitochondria.

AARS2 Antigen Profile

Antigen Summary

The protein encoded by this gene belongs to the class-II aminoacyl-tRNA synthetase family. Aminoacyl-tRNA synthetases play critical roles in mRNA translation by charging tRNAs with their cognate amino acids. The encoded protein is a mitochondrial enzyme that specifically aminoacylates alanyl-tRNA. Mutations in this gene are a cause of combined oxidative phosphorylation deficiency 8.

Gene names and symbols associated with AARS2

  • alanyl-tRNA synthetase 2, mitochondrial (AARS2) antibody
  • alanyl-tRNA synthetase 2, mitochondrial (Aars2) antibody
  • Aarsl antibody
  • AlaRS antibody
  • COXPD8 antibody
  • Gm89 antibody
  • MT-ALARS antibody
  • MTALARS antibody

Protein level used designations for AARS2

probable alanyl-tRNA synthetase, mitochondrial , alanyl-tRNA synthetase like , alanyl-tRNA synthetase 2, mitochondrial (putative) , alanyl-tRNA synthetase, mitochondrial , alanine tRNA ligase 2, mitochondrial (putative) , alanine--tRNA ligase, mitochondrial

421436 Gallus gallus
462733 Pan troglodytes
702626 Macaca mulatta
786099 Bos taurus
100013354 Monodelphis domestica
100067843 Equus caballus
100155115 Sus scrofa
100447064 Pongo abelii
57505 Homo sapiens
474920 Canis lupus familiaris
301254 Rattus norvegicus
224805 Mus musculus
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