Alanine--TRNA Ligase, Mitochondrial (AARS2) Antibody

Este producto es parte de AARS - Alanine-TRNA Ligase
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195€ (20 µl)

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935106861
info@markelab.com
name
Alanine--TRNA Ligase, Mitochondrial (AARS2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx006545
tested applications
ELISA, WB

Description

AARS2 Antibody is a Rabbit Polyclonal Antibody against AARS2.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Alanine--TRNA Ligase, Mitochondrial (AARS2)
Host
Rabbit
Reactivity
Human
Recommended Dilution
ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q5JTZ9
Gene ID
57505
NCBI Accession
NP_065796.1
Alias
AARS2,AARSL,KIAA1270
Background
Antibody anti-AARS2
Status
RUO
Note
Concentration: > 0.2 mg/ml - 

Descripción

AARS2 is an essential mitochondrial enzyme responsible for catalyzing the ligation of alanine to its corresponding tRNA (tRNA^Ala) during mitochondrial protein synthesis. This process is crucial for the translation of mitochondrial-encoded proteins, which are integral components of the oxidative phosphorylation system. Structurally, AARS2 contains a catalytic domain that ensures high specificity for alanine and tRNA^Ala, contributing to the accuracy of mitochondrial protein translation. AARS2 is predominantly expressed in energy-demanding tissues such as the brain, heart, and skeletal muscle, underscoring its role in maintaining mitochondrial function. Mutations in the AARS2 gene have been linked to mitochondrial diseases, including leukodystrophy and cardiomyopathy, which are characterized by impaired mitochondrial protein synthesis and energy production. These conditions highlight the critical importance of AARS2 in cellular energy metabolism and mitochondrial integrity. Emerging research also suggests potential links between AARS2 dysfunction and broader neurodegenerative disorders, making it a significant target for therapeutic exploration.

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