RARS2 Antibodies

AND RARS2 ELISA kits, RARS2 Proteins

Many biological assays use antibodies to detect RARS2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with RARS2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop RARS2 antibodies...

We validate the specificity of these antibodies to RARS2 by testing them on tissues known to express RARS2 positively and negatively. Browse below to find the RARS2 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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RARS2 Infographic by Boster Bio

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Anti-RARS2 Antibody

Human, Mouse

$405
Cat # A10485
100ul

RARS2 Overview

Facts about Probable arginine--tRNA ligase, mitochondrial.

RARS2 3D structure. Source: alphafold

Probable arginine--tRNA ligase, mitochondrial (RARS2)

Gene Information

Human
Gene Name:	RARS2
Uniprot:	Q5T160
Entrez:	57038

Family

Belongs to:

class-I aminoacyl-tRNA synthetase family

Alternative Names

arginine-tRNA ligase; arginyl-tRNA synthetase 2, mitochondrial; Arginyl-tRNA synthetase-like; ArgRS; DALRD2; dJ382I10.6; EC 6.1.1.19; MGC14993; MGC23778; PCH6; PRO1992; probable arginyl-tRNA synthetase, mitochondrial; RARSLArginine--tRNA ligase

Molecular Weight

Mass (kDA):
65.505 kDA

Genomic Context


Human

Location:	6q15
Sequence:	6; NC_000006.12 (87513935..87590032, complement)

Subcellular Localizations

Mitochondrion matrix.

Diseases

Hypoplasia
Atrophy
Olivopontocerebellar Atrophies
Microcephaly
Cerebral Atrophy
Optic Atrophy
Congenital Cerebellar Hypoplasia
Mitochondrial Diseases
Acidosis
Mitochondrial Encephalomyopathies
Dystonia Disorders
Epilepsy

Encephalopathies
Brain Diseases
Acidosis, Lactic
Neurodegenerative Disorders
Ataxia
Leukoencephalopathies
Merrf Syndrome

Pathways

Translation
Cell Death
Mitochondrial Translation
Rna Splicing

PTMs

Acetylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/RARS2

References

PMID: 15779907 by Bonnefond L., et al. Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS.

PMID: 17847012 by Edvardson S., et al. Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia.