RPL10 Antibody
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货号:CSB-PA040238
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规格:¥880
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其他:
产品详情
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Uniprot No.:P27635
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基因名:RPL10
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别名:RPL10 antibody; DXS648E antibody; QM antibody; 60S ribosomal protein L10 antibody; Laminin receptor homolog antibody; Large ribosomal subunit protein uL16 antibody; Protein QM antibody; Ribosomal protein L10 antibody; Tumor suppressor QM 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:Synthesized peptide derived from the Internal region of Human QM.
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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抗体亚型:IgG
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纯化方式:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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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:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
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产品提供形式:Liquid
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应用范围:WB, ELISA
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:2000 ELISA 1:20000 -
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:Component of the large ribosomal subunit. Plays a role in the formation of actively translating ribosomes. May play a role in the embryonic brain development.
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基因功能参考文献:
- The regulation of reactive oxygen species level by mitochondrial RPL10 is one of the major extra-ribosomal functions in pancreatic cancer cells, which could be used as an indicator for the tumorigenesis of pancreatic cancer. PMID: 30172100
- there are 7 mutations in RPL10 in 344 patients, or a mutation frequency of 2% PMID: 28428269
- A rare de novo mutation K78E is associated with severe syndromic intellectual disability and epilepsy. PMID: 29066376
- Mitochondrial Ribosomal Protein L10 regulates cyclin B1/Cdk1 (cyclin-dependent kinase 1) activity and mitochondrial protein synthesis in mammalian cells PMID: 27726420
- Our results expand the mutational and clinical spectrum of RPL10 identifying a new genetic cause of SED and highlight the emerging role of ribosomal proteins in the pathogenesis of neurodevelopmental disorders. PMID: 26290468
- report confirms the implication of RPL10 mutations in neurodevelopmental disorders and extends the associated clinical spectrum from autism to syndromic intellectual disability PMID: 25846674
- A mutation within the conserved N-terminal end of RPL10, a protein in close proximity to the peptidyl transferase active site of the 60S ribosomal subunit, causes severe defects in brain formation and function. PMID: 25316788
- Mutations affect the ribosomal proteins RPL5 and RPL10 in 12 of 122 (9.8%) pediatric T-cell acute lymphoblastic leukemias, with recurrent alterations of Arg98 in RPL10. PMID: 23263491
- mutation analysis of RPL10 in German patients with autism spectrum disorder PMID: 21567917
- Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism PMID: 16940977
- QM binds to c-yes at the SH3 domain in tumor cell lines PMID: 12138090
- Reduction of QM protein expression correlates with tumor grade in prostatic adenocarcinoma PMID: 16331298
- Xq28 (QM gene) may be involved in ovary failure. PMID: 17566674
- A hexagonal crystal of L10CD was obtained by the sitting-drop vapour-diffusion method. The L10CD crystal diffracted to 2.5 A resolution and belongs to space group P3(1)21 or P3(2)21. PMID: 18007048
- Characteristic interactions among Arg90-Trp171-Arg139 guide the C-terminal part outside of the central fold PMID: 18258260
- Our results suggest that RPL10 has no major effect on the susceptibility to autism spectrum disorders PMID: 19166581
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相关疾病:Autism, X-linked 5 (AUTSX5); Mental retardation, X-linked, syndromic, 35 (MRXS35)
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蛋白家族:Universal ribosomal protein uL16 family
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数据库链接:
HGNC: 10298
OMIM: 300847
KEGG: hsa:6134
STRING: 9606.ENSP00000341730
UniGene: Hs.534404
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