HARS2 anticorps

N° du produit ABIN7263809

Détail du produit anti-HARS2 anticorps

Antigène: HARS2 (Histidyl-tRNA Synthetase 2, Mitochondrial (Putative) (HARS2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HARS2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human HARS2 (NP_036340.1).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur HARS2

Antigène: HARS2 (Histidyl-tRNA Synthetase 2, Mitochondrial (Putative) (HARS2))

Autre désignation: HARS2 (HARS2 Produits)

Synonymes: anticorps HARSL, anticorps HARSR, anticorps HO3, anticorps PRLTS2, anticorps HARS2, anticorps 4631412B19Rik, anticorps AI593507, anticorps Harsl, anticorps DTD1, anticorps Hars2l, anticorps RGD1308426, anticorps Zmat2, anticorps histidyl-tRNA synthetase 2, mitochondrial, anticorps histidyl-tRNA synthetase 2, anticorps histidyl-tRNA synthetase-like, anticorps HARS2, anticorps Hars2, anticorps LOC100635288

Sujet: Aminoacyl-tRNA synthetases are a class of enzymes that charge tRNAs with their cognate amino acids. The protein encoded by this gene is an enzyme belonging to the class II family of aminoacyl-tRNA synthetases. Functioning in the synthesis of histidyl-transfer RNA, the enzyme plays an accessory role in the regulation of protein biosynthesis. The gene is located in a head-to-head orientation with HARS on chromosome five, where the homologous genes likely share a bidirectional promoter. Mutations in this gene are associated with the pathogenesis of Perrault syndrome, which involves ovarian dysgenesis and sensorineural hearing loss. Alternative splicing results in multiple transcript variants of this gene.

Poids moléculaire:

Observed_MW: 50 kDa

Calculated_MW: 54 kDa/56 kDa

ID gène: 23438

UniProt: P49590