FARS2 Polyclonal antibody
FARS2 Polyclonal Antibody for WB, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human, mouse and More (1)
Applications
WB, ELISA
Conjugate
Unconjugated
Cat no : 16436-1-AP
Synonyms
Validation Data Gallery
Applications:
Tested Applications
| Positive WB detected in | HeLa cells, Jurkat cells, HepG2 cells |
Recommended dilution
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:2000-1:10000 |
| Sample-dependent, check data in validation data gallery | |
Published Applications
| WB | See 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 Reactivity | human, 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 number | BC021112 |
| Gene symbol | FARS2 |
| Gene ID (NCBI) | 10667 |
| RRID | AB_2102499 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Antigen affinity purification |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
| Storage Conditions | Store 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-AP | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |
Publications
| Species | Application | Title |
|---|---|---|
Mol Genet Metab Clinical and molecular characterization of novel FARS2 variants causing neonatal mitochondrial disease | ||
Biochim Biophys Acta Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency. | ||
Eur J Hum Genet Novel FARS2 variants in patients with early onset encephalopathy with or without epilepsy associated with long survival. | ||
Nat Commun Phenylalanine impairs insulin signaling and inhibits glucose uptake through modification of IRβ. |
