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DAXX死亡相关蛋白6抗体(Fas死亡区相关蛋白)

点击次数:285发布时间:2012/12/5 13:31:59

DAXX死亡相关蛋白6抗体(Fas死亡区相关蛋白)

更新日期:2024/9/5 14:43:01

所 在 地:中国大陆

产品型号:BY-1975R

简单介绍:本公司经销DAXX,死亡相关蛋白6抗体(Fas死亡区相关蛋白),克隆类型为polyclonal,宿主来源是Rabbit,DAXX死亡相关蛋白6抗体(Fas死亡区相关蛋白)可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

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本公司经销DAXX,死亡相关蛋白6抗体(Fas死亡区相关蛋白),克隆类型为polyclonal,宿主来源是Rabbit,DAXX死亡相关蛋白6抗体(Fas死亡区相关蛋白)可应用于WB、elisa、IP、IF、IHC等实验,欢迎垂询订购!

货号:BY-1975R
英文名称:Anti-DAXX
中文名称:死亡相关蛋白6抗体(Fas死亡区相关蛋白)
其他名称:名BING 2; BING2; DAP 6; DAP6; Death associated protein 6; Fas death domain-associated protein; Death domain associated protein 6; EAP 1; EAP1; ETS1 associated protein 1; Fas death domain associated protein; hDaxx; MGC126245; MGC126246.
抗体来源:Rabbit
克隆类型:polyclonal
蛋白分子量:predicted molecular weight: 82kDa
纯化方法:affinity purified by Protein A
交叉反应:hu, mo, rat, cow, pig, shp, Rb, dog
产品介绍:Acts as an adapter protein in a MDM2-DAXX-USP7 complex by regulating the RING-finger E3 ligase MDM2 ubiquitination activity. Under non-stress condition, in association with the deubiquitinating USP7, prevents MDM2 self-ubiquitination and enhances the intrinsic E3 ligase activity of MDM2 towards TP53, thereby promoting TP53 ubiquitination and subsequent proteasomal degradation. Upon DNA damage, its association with MDM2 and USP7 is disrupted, resulting in increased MDM2 autoubiquitination and consequently, MDM2 degradation, which leads to TP53 stabilization. Proposed to mediate activation of the JNK pathway and apoptosis via MAP3K5 in response to signaling from TNFRSF6 and TGFBR2. Interaction with HSPB1/HSP27 may prevent interaction with TNFRSF6 and MAP3K5 and block DAXX-mediated apoptosis. In contrast, in lymphoid cells JNC activation and TNFRSF6-mediated apoptosis may not involve DAXX. Seems to regulate transcription in PML/POD/ND10 nuclear bodies together with PML and may influence TNFRSF6-dependent apoptosis thereby. Down-regulates basal and activated transcription. Seems to act as a transcriptional corepressor and inhibits PAX3 and ETS1 through direct protein-protein interaction. Modulates PAX5 activity. Its transcription repressor activity is modulated by recruiting it to subnuclear compartments like the nucleolus or PML/POD/ND10 nuclear bodies through interactions with MCSR1 and PML, respectively.Subcellular Location : Cytoplasm. Nucleus > nucleoplasm. Nucleus > PML body. Nucleus > nucleolus. Chromosome > centromere. Dispersed throughout the nucleoplasm, in PML/POD/ND10 nuclear bodies, and in nucleoli. Colocalizes with a subset of interphase centromeres, but is absent from mitotic centromeres. Detected in cytoplasmic punctate structures. Translocates from the nucleus to the cytoplasm upon glucose deprivation or oxidative stress. Colocalizes with RASSF1 in the nucleus. Colocalizes with USP7 in nucleoplasma with accumulation in speckled structures.Tissue Specificity : Ubiquitous.Post-translational modifications : Sumoylated.Phosphorylated upon DNA damage, probably by ATM or ATR. Phosphorylated by HIPK1 upon glucose deprivation.Polyubiquitinated; which is promoted by CUL3 and SPOP and results in proteasomal degradation. Ubiquitinated by MDM2; inducing its degradation. Deubiquitinated by USP7; leading to stabilize it.Similarity : Belongs to the DAXX family.

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