MID2 Antibody
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货号:CSB-PA892324ESR2HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) MID2 Polyclonal antibody
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Uniprot No.:Q9UJV3
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基因名:MID2
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别名:FLJ37715 antibody; FLJ41813 antibody; FXY2 antibody; MID2 antibody; Midin 2 antibody; Midin-2 antibody; Midline 2 antibody; Midline defect 2 antibody; Midline-2 antibody; probable E3 ubiquitin protein ligase MID2 antibody; Probable E3 ubiquitin-protein ligase MID2 antibody; RING finger protein 60 antibody; Ring finger protein protein 60 antibody; RNF60 antibody; TRIM1 antibody; TRIM1_HUMAN antibody; tripartite motif containing protein 1 antibody; Tripartite motif protein 1 antibody; Tripartite motif-containing protein 1 antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Probable E3 ubiquitin-protein ligase MID2 protein (506-735AA)
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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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克隆类型:Polyclonal
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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, pH7.3.
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产品提供形式:Liquid
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应用范围:ELISA, IHC, IF
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推荐稀释比:
Application Recommended Dilution IHC 1:20-1:200 IF 1:50-1:200 -
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:May play a role in microtubule stabilization.
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基因功能参考文献:
- overexpressed in advanced breast cancer and high overexpression is prognostic factor for poor overall survival PMID: 26791755
- Mid2 regulates cell division through the ubiquitination of astrin on K409, which is critical for its degradation and proper cytokinesis. PMID: 26748699
- A novel missense mutation (c.1040G>A, p.Arg347Gln) was reported in MID2, which encodes ubiquitin ligase E3, as the likely cause of X-linked mental retardation in a large kindred. PMID: 24115387
- MID2 coiled-coil motifs mediate both homo- and heterodimerization, a prerequisite for association of the MID-alpha 4 complex with microtubules. PMID: 11806752
- MID2 is a candidate gene for FG syndrome. PMID: 16283679
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相关疾病:Mental retardation, X-linked 101 (MRX101)
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亚细胞定位:Cytoplasm. Cytoplasm, cytoskeleton. Note=Microtubule-associated.
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蛋白家族:TRIM/RBCC family
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组织特异性:Low level in fetal kidney and lung, and in adult prostate, ovary and small intestine.
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数据库链接:
HGNC: 7096
OMIM: 300204
KEGG: hsa:11043
STRING: 9606.ENSP00000262843
UniGene: Hs.12256
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