CCDC50 Antibody
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货号:CSB-PA004709GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:Q8IVM0
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基因名:CCDC50
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别名:C3orf6 antibody; C3orf6 YMER antibody; CCD50_HUMAN antibody; CCDC 50 antibody; Ccdc50 antibody; Chromosome 3 open reading frame 6 antibody; Coiled coil domain containing 50 antibody; Coiled coil domain containing protein 50 antibody; Coiled-coil domain-containing protein 50 antibody; Protein Ymer antibody; Ymer antibody; Ymer protein 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 CCDC50
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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 0.02% 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
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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:Involved in EGFR signaling.
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基因功能参考文献:
- Up to now, merely 7 loci have been linked to mid-frequency hearing loss. Only four genetic mid-frequency deafness genes, namely, DFNA10 (EYA4), DFNA8/12 (TECTA), DFNA13 (COL11A2), DFNA44 (CCDC50), have been reported to date. [review] PMID: 27142990
- Ymer acts as a regulator downstream of several receptors and that Ymer functions as a positive or negative regulator in a signaling pathway-dependent manner. PMID: 22331027
- identification of a novel DFNA locus on chromosome 3q28-29 in a Spanish family with postlingual and progressive hearing loss[DFNA44] PMID: 12483295
- Ymer functions as a novel inhibitor for the down-regulation of the EGF receptor and plays a crucial role for regulating the amount of the EGF receptor on the cell surface membrane PMID: 16803894
- These findings demonstrate that Ymer is likely to be a negative regulator for the NF-kappaB signaling pathway. PMID: 19059208
- CCDC50 is required for survival in mantle cell lymphoma and chronic lymphocytic leukemia cells and controls NFkappaB signaling PMID: 19641524
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相关疾病:Deafness, autosomal dominant, 44 (DFNA44)
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亚细胞定位:Cytoplasm.
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组织特异性:Isoform 1 and isoform 2 are coexpressed in placenta, liver, lung, kidney and pancreas. Only isoform 1 is detected in skeletal muscle, brain and heart.
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数据库链接:
HGNC: 18111
OMIM: 607453
KEGG: hsa:152137
UniGene: Hs.478682
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