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FARS2 Polyclonal antibody

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

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse and More (1)

Applications

WB, ELISA

FARS1, FARS2, HSPC320, Phenylalanine tRNA ligase, PheRS

Formulation:  PBS and Azide
PBS and Azide
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -


ご購入について

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国内在庫・納期について

約2万点のプロテインテック製品をコスモバイオ社物流センター(国内)に在庫しています。国内在庫の有無はコスモバイオ社ホームページの「品番検索」でカタログ番号を検索して確認できます。


保証・サポートについて

テクニカルサポートまたはご購入後1年間の交換/補填対応を承ります。詳細はこちらをご覧ください。


Tested Applications

Positive WB detected inHeLa cells, Jurkat cells, HepG2 cells

Recommended dilution

ApplicationDilution
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.

Published Applications

WBSee 5 publications below

Product Information

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

Tested Reactivity human, mouse
Cited Reactivityhuman, rat, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen FARS2 fusion protein Ag9750 相同性解析による交差性が予測される生物種
Full Name phenylalanyl-tRNA synthetase 2, mitochondrial
Calculated molecular weight 451 aa, 52 kDa
Observed molecular weight 48 kDa
GenBank accession numberBC021112
Gene Symbol FARS2
Gene ID (NCBI) 10667
RRIDAB_2102499
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDO95363
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

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).

Protocols

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

Publications

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
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