WDR4 Antibody
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货号:CSB-PA026021GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P57081
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基因名:WDR4
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别名:OTTHUMP00000109401 antibody; OTTHUMP00000109402 antibody; TRM82 antibody; tRNA (guanine N(7) ) methyltransferase subunit WDR4 antibody; tRNA (guanine-N(7)-)-methyltransferase subunit WDR4 antibody; WD repeat containing protein 4 antibody; WD repeat protein 4 antibody; WD repeat protein domain 4 protein isoform 2 antibody; WD repeat-containing protein 4 antibody; wdr4 antibody; WDR4_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 WDR4
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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
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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:Non-catalytic component of a methyltransferase complex required for the formation of N(7)-methylguanine in a subset of RNA species, such as tRNAs, mRNAs and microRNAs (miRNAs). In the methyltransferase complex, it is required to stabilize and induce conformational changes of the catalytic subunit. Required for the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA. Also required for the formation of N(7)-methylguanine at internal sites in a subset of mRNAs. Also required for methylation of a specific subset of miRNAs, such as let-7. Independently of METTL1, also plays a role in genome stability: localizes at the DNA replication site and regulates endonucleolytic activities of FEN1.
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基因功能参考文献:
- WDR4 is an oncoprotein that negatively regulates PML via ubiquitination to promote lung cancer progression by fostering an immunosuppressive and prometastatic tumor microenvironment PMID: 28691927
- Combined autozygome/exome analysis revealed a novel missense mutation in WDR4 as the likely causal variant of Primordial dwarfism PMID: 26416026
- regulates FEN1's potential DNA cleavage threat near the site of replication PMID: 26751069
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亚细胞定位:Nucleus. Chromosome.
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蛋白家族:WD repeat TRM82 family
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数据库链接:
HGNC: 12756
OMIM: 605924
KEGG: hsa:10785
STRING: 9606.ENSP00000328671
UniGene: Hs.248815
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