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RARS2 antibody (AA 1-560)

This anti-RARS2 antibody is a Rabbit Polyclonal antibody detecting RARS2 in WB, ELISA and FACS. Suitable for Human, Mouse and Rat.
Catalog No. ABIN7599480

Quick Overview for RARS2 antibody (AA 1-560) (ABIN7599480)

Target

See all RARS2 Antibodies
RARS2 (Arginyl-tRNA Synthetase 2, Mitochondrial (RARS2))

Reactivity

Human, Mouse, Rat

Host

  • 12
  • 2
Rabbit

Clonality

  • 14
Polyclonal

Conjugate

  • 11
  • 1
  • 1
  • 1
This RARS2 antibody is un-conjugated

Application

  • 9
  • 7
  • 7
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 4
    • 3
    • 2
    • 2
    • 2
    AA 1-560

    Purpose

    Anti-RARS2 Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins

    Characteristics

    Anti-RARS2 Antibody Picoband® (ABIN7599480). Tested in WB, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human RARS2 recombinant protein (Position: M1-R560). Human RARS2 shares 86.1% amino acid (aa) sequence identity with mouse RARS2.

    Isotype

    IgG
  • Application Notes

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL
    1. Edvardson, S., Shaag, A., Kolesnikova, O., Gomori, J. M., Tarassov, I., Einbinder, T., Saada, E., Elpeleg, O. Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia. Am. J. Hum. Genet. 81: 857-862, 2007. 2. Li, Z., Schonberg, R., Guidugli, L., Johnson, A. K., Arnovitz, S., Yang, S., Scafidi, J., Summar, M. L., Vezina, G., Das, S., Chapman, K., del Gaudio, D. A novel mutation in the promoter of RARS2 causes pontocerebellar hypoplasia in two siblings. J. Hum. Genet. 60: 363-369, 2015. 3. Rankin, J., Brown, R., Dobyns, W. B., Harington, J., Patel, J., Quinn, M., Brown, G. Pontocerebellar hypoplasia type 6: a British case with PEHO-like features. Am. J. Med. Genet. 152A: 2079-2084, 2010.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

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

    Alternative Name

    RARS2

    Background

    Synonyms: RARS2, RARSL, Probable arginine--tRNA ligase, mitochondrial, EC 6.1.1.19, Arginyl-tRNA synthetase, ArgRS

    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.

    Molecular Weight

    66 kDa

    Gene ID

    57038

    UniProt

    Q5T160
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