Alanine--TRNA Ligase, Mitochondrial (AARS2) Antibody

Este producto es parte de AARS - Alanine-TRNA Ligase
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442€ (200 µl)

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935106861
info@markelab.com
name
Alanine--TRNA Ligase, Mitochondrial (AARS2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx432253
tested applications
P-ELISA, WB

Description

AARS2 Antibody is a Goat Polyclonal antibody against AARS2.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Target: Alanine--TRNA Ligase, Mitochondrial (AARS2)
Immunogen: abx616777 - Internal region, 478-489 AA: C-QHRARQAEPVQK
Host
Goat
Reactivity
Human
Assay Type
Concentration: 0.5 mg/ml
Recommended Dilution
P-ELISA: 1/32000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Size 1
200 µl
Form
Liquid
Tested Applications
P-ELISA, WB
Buffer
Tris saline, pH 7.3, containing 0.02% sodium azide and 0.5% bovine serum albumin.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Gene ID
57505
NCBI Accession
NP_065796.1
Alias
AARS2,AARSL,KIAA1270
Background
Antibody anti-AARS2
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

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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