HARS2 Antikörper

Produktnummer ABIN7263809

Produktdetails anti-HARS2 Antikörper

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HARS2 Antikörper ist unkonjugiert

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

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000 IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu HARS2

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

Andere Bezeichnung: HARS2 (HARS2 Produkte)

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

Hintergrund: 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.

Molekulargewicht:

Observed_MW: 50 kDa

Calculated_MW: 54 kDa/56 kDa

Gen-ID: 23438

UniProt: P49590