RARS2 Antibody

Code CSB-PA732918ESR2HU
Size US$166
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Image
  • Western blot
    All lanes: RARS2 antibody at 2.68 μg/ml
    Lane 1: Mouse kidney tissue
    Lane 2: HL60 whole cell lysate
    Secondary
    Goat polyclonal to rabbit IgG at 1/10000 dilution
    Predicted band size: 66 kDa
    Observed band size: 66 kDa

  • Immunohistochemistry of paraffin-embedded human lung cancer using CSB-PA732918ESR2HU at dilution of 1:100

  • Immunohistochemistry of paraffin-embedded human gastric cancer using CSB-PA732918ESR2HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) RARS2 Polyclonal antibody
Uniprot No.
Target Names
RARS2
Alternative Names
arginine tRNA ligase antibody; arginyl tRNA synthetase 2 mitochondrial antibody; Arginyl tRNA synthetase antibody; Arginyl-tRNA synthetase antibody; ArgRS antibody; DALRD2 antibody; mitochondrial antibody; PCH6 antibody; Probable arginine tRNA ligase antibody; probable arginine tRNA ligase mitochondrial antibody; Probable arginine--tRNA ligase antibody; probable arginyl tRNA synthetase mitochondrial antibody; RARS2 antibody; RARSL antibody; SYRM_HUMAN antibody
Raised in
Rabbit
Species Reactivity
Human, Mouse
Immunogen
Recombinant Human Probable arginine--tRNA ligase, mitochondrial protein (17-340AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Tested Applications
ELISA, WB, IHC
Recommended Dilution
Application Recommended Dilution
WB 1:1000-1:5000
IHC 1:20-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Gene References into Functions
  1. Characteristic neuroradiological abnormalities of PCH6 such as vermis and cerebellar hypoplasia and progressive pontocerebellar atrophy may be missing in patients with RARS2 mutations PMID: 27769281
  2. RARS2 gene mutations can cause a metabolic neurodegenerative disease manifesting primarily as early onset epileptic encephalopathies with post-natal microcephaly, without pontocerebellar hypoplasia. PMID: 26970947
  3. Mutations in the RARS2 promoter are likely to represent a new causal mechanism of pontocerebellar hypoplasia. PMID: 25809939
  4. Molecular investigations of RARS2 disclosed the c.25A>G/p.I9V and the c.1586+3A>T in family A. PMID: 22569581
  5. mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2, may have a role in pontocerebellar hypoplasia type 6 [case report] PMID: 22086604

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Involvement in disease
Pontocerebellar hypoplasia 6 (PCH6)
Subcellular Location
Mitochondrion matrix.
Protein Families
Class-I aminoacyl-tRNA synthetase family
Database Links

HGNC: 21406

OMIM: 611523

KEGG: hsa:57038

STRING: 9606.ENSP00000358549

UniGene: Hs.485910

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