HARS2 antibody

Catalog No. ABIN5702955

Product Details anti-HARS2 Antibody

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HARS2 antibody is un-conjugated

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

Immunogen: histidyl-tRNA synthetase 2, mitochondrial (putative)

Isotype: IgG

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Comment:

MCF7 cells were subjected to SDS PAGE followed by western blot with FNab03759(HARS2 antibody) at dilution of 1:200

Restrictions: For Research Use only

Handling

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

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freeze / thaw cycles.

Storage: -20 °C

Expiry Date: 12 months

Target Details for HARS2

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

Alternative Name: HARS2 (HARS2 Products)

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

Background: Synonyms:HARSL, HARSR, HO3 Background: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.

Molecular Weight: 50-55 kDa

Gene ID: 23438

UniProt: P49590