QARS Antibody
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货号:CSB-PA019132GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P47897
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基因名:QARS
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别名:GlnRS antibody; Glutamine tRNA ligase antibody; Glutamine tRNA synthetase antibody; Glutamine--tRNA ligase antibody; Glutaminyl tRNA ligase antibody; Glutaminyl tRNA synthetase antibody; Glutaminyl-tRNA synthetase antibody; PRO2195 antibody; QARS antibody; SYQ_HUMAN antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Human QARS
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免疫原种属:Homo sapiens (Human)
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抗体亚型:IgG
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纯化方式:Antigen Affinity Purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB,IHC
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Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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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靶点详情
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功能:Glutamine--tRNA ligase. Plays a critical role in brain development.
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基因功能参考文献:
- patient's fibroblasts demonstrated markedly reduced QARS amino acylation activity in vitro PMID: 28620870
- hcmv-miR-US4-1 may involve in promoting cell apoptosis and benefiting discharge of infectious virus particles via down-regulation of QARS in HCMV-infected HELF cells. PMID: 27240979
- Pathological mutations mapping in the N-terminal domain alter the domain structure, and decrease catalytic activity and stability of GlnRS, whereas missense mutations in the catalytic domain induce misfolding of the enzyme. PMID: 26869582
- Data indicate compound heterozygous mutations [c.169T>C (p.Tyr57His) and c.1485dup (p.Lys496*)] in QARS, which encodes glutaminyl-tRNA synthetase, in two siblings with early-onset epileptic encephalopathy (EOEE). PMID: 25471517
- interactions between the N-terminal domains of ArgRS and AIMP1 are important for the catalytic and noncatalytic activities of ArgRS and for the assembly of the higher-order MSC protein complex with ArgRS-GlnRS-AIMP1 PMID: 25288775
- results highlight the importance of QARS during brain development and that epilepsy due to impairment of QARS activity is unusually severe in comparison to other aminoacyl-tRNA synthetase disorders PMID: 24656866
- Data indicate that glutaminyl-tRNA synthetase splice variant GlnRSDeltaiABD was present in exosomes extruded from Jurkat cells and functional in protein synthesis. PMID: 24003230
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相关疾病:Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy (MSCCA)
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亚细胞定位:Cytoplasm, cytosol. Cytoplasm.
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蛋白家族:Class-I aminoacyl-tRNA synthetase family
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组织特异性:Highly expressed in fetal cerebral cortex, particularly in the ventricular zone, inner subventricular zone, outer subventricular zone, and cortical plate.
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数据库链接:
HGNC: 9751
OMIM: 603727
KEGG: hsa:5859
STRING: 9606.ENSP00000307567
UniGene: Hs.79322
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