RARS2 antibody (AA 17-340)

Catalog No. ABIN6146710

Product Details anti-RARS2 Antibody

Target: RARS2 (Arginyl-tRNA Synthetase 2, Mitochondrial (RARS2))

Binding Specificity: AA 17-340

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RARS2 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: LNLPPENLIT SISAVPISQK EEVADFQLSV DSLLEKDNDH SRPDIQVQAK RLAEKLRCDT VVSEISTGQR TVNFKINREL LTKTVLQQVI EDGSKYGLKS ELFSGLPQKK IVVEFSSPNV AKKFHVGHLR STIIGNFIAN LKEALGHQVI RINYLGDWGM QFGLLGTGFQ LFGYEEKLQS NPLQHLFEVY VQVNKEAADD KSVAKAAQEF FQRLELGDVQ ALSLWQKFRD LSIEEYIRVY KRLGVYFDEY SGESFYREKS QEVLKLLESK GLLLKTIKGT AVVDLSGNGD PSSICTVMRS DGTSLYATRD LAAAIDRMDK YNFD

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 17-340 of human RARS2 (NP_064716.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,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.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for RARS2

Target: RARS2 (Arginyl-tRNA Synthetase 2, Mitochondrial (RARS2))

Alternative Name: RARS2 (RARS2 Products)

Synonyms: RARSL antibody, DKFZp468H102 antibody, ArgRS antibody, DALRD2 antibody, PCH6 antibody, PRO1992 antibody, dJ382I10.6 antibody, 1500002I10Rik antibody, Rarsl antibody, arginyl-tRNA synthetase 2, mitochondrial S homeolog antibody, arginyl-tRNA synthetase 2, mitochondrial antibody, rars2.S antibody, RARS2 antibody, Rars2 antibody

Background: This nuclear gene encodes a protein that localizes to the mitochondria, where it catalyzes the transfer of L-arginine to its cognate tRNA, an important step in translation of mitochondrially-encoded proteins. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6). Alternative splicing results in multiple transcript variants.,RARS2,ArgRS,DALRD2,PCH6,PRO1992,RARSL,Epigenetics & Nuclear Signaling,Endocrine & Metabolism,Mitochondrial metabolism,RARS2

Molecular Weight: 65 kDa

Gene ID: 57038

UniProt: Q5T160