CCDC50 Antibody
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中文名稱:CCDC50兔多克隆抗體
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貨號:CSB-PA004709GA01HU
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規(guī)格:¥3,900
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其他:
產品詳情
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Uniprot No.:
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基因名:CCDC50
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別名: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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反應種屬:Human,Mouse,Rat
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免疫原:Human CCDC50
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免疫原種屬:Homo sapiens (Human)
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抗體亞型:IgG
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純化方式:Antigen Affinity purified
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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產品提供形式:Liquid
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應用范圍:ELISA,WB
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Protocols:
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儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期: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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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
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靶點詳情
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功能:Involved in EGFR signaling.
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基因功能參考文獻:
- 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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相關疾?。?/div>Deafness, autosomal dominant, 44 (DFNA44)亞細胞定位:Cytoplasm.組織特異性: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.數據庫鏈接:
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