FARS2 Polyclonal antibody

FARS2 Polyclonal Antibody for WB, ELISA
Cat No. 16436-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse and More (1)

应用

WB, ELISA

FARS1, FARS2, HSPC320, Phenylalanine tRNA ligase, PheRS

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -


经过测试的应用

Positive WB detected inHeLa cells, Jurkat cells, HepG2 cells

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:2000-1:10000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

发表文章中的应用

WBSee 5 publications below

产品信息

16436-1-AP targets FARS2 in WB, ELISA applications and shows reactivity with human, mouse samples.

经测试应用 WB, ELISA Application Description
文献引用应用WB
经测试反应性 human, mouse
文献引用反应性human, mouse, rat
免疫原 FARS2 fusion protein Ag9750 种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 phenylalanyl-tRNA synthetase 2, mitochondrial
别名 FARS1, FARS2, HSPC320, Phenylalanine tRNA ligase, PheRS
计算分子量 451 aa, 52 kDa
观测分子量 48 kDa
GenBank蛋白编号BC021112
基因名称 FARS2
Gene ID (NCBI) 10667
RRIDAB_2102499
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDO95363
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

FARS2, a nuclear gene located on chromosome 6 (6p25.1), encodes the mitochondrial phenylalanyl-tRNA synthetase (mtPheRS), which transfers phenylalanine (Phe) to its cognate tRNA in mitochondria (PMID: 32774346).

实验方案

Product Specific Protocols
WB protocol for FARS2 antibody 16436-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
humanWB

Mol Genet Metab

Clinical and molecular characterization of novel FARS2 variants causing neonatal mitochondrial disease

Authors - Wenqian Chen
humanWB

Mol Genet Metab

New insights into the phenotype of FARS2 deficiency.

Authors - Elise Vantroys
humanWB

Biochim Biophys Acta

Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency.

Authors - Abdulraheem Almalki
humanWB

Eur J Hum Genet

Novel FARS2 variants in patients with early onset encephalopathy with or without epilepsy associated with long survival.

Authors - Giulia Barcia
human,rat,mouseWB

Nat Commun

Phenylalanine impairs insulin signaling and inhibits glucose uptake through modification of IRβ.

Authors - Qian Zhou
Loading...