anti-MDM4-binding Protein (MDM4) 抗体产品概述

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anti-Mdm4-binding Protein 抗体 (MDM4)
在www.antibodies-online.cn可供145 Mdm4-binding Protein (MDM4) 抗体的24不同的供货商。 再加上,我们可以发MDM4-binding Protein 蛋白 (10)MDM4-binding Protein 试剂盒 (7)和数多这个蛋白质的别的产品。 总共170 MDM4-binding Protein产品已列进来了。
4933417N07Rik, AA414968, AL023055, AU018793, AU021806, C85810, HDMX, Mdmx, MRP1, wu:fa09h09, wu:fi33d10

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抗Rat (Rattus) MDM4-binding Protein 抗体:

抗Mouse (Murine) MDM4-binding Protein 抗体:

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引用最多的anti-MDM4-binding Protein 抗体

  1. Human Polyclonal MDM4-binding Protein Primary Antibody for IP, WB - ABIN151988 : Patton, Mayo, Singhi, Gudkov, Stark, Jackson: Levels of HdmX expression dictate the sensitivity of normal and transformed cells to Nutlin-3. in Cancer research 2006 (PubMed)
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  2. Human Monoclonal MDM4-binding Protein Primary Antibody for ICC, IHC - ABIN969282 : Strausberg, Feingold, Grouse, Derge, Klausner, Collins, Wagner, Shenmen, Schuler, Altschul, Zeeberg, Buetow, Schaefer, Bhat, Hopkins, Jordan, Moore, Max, Wang, Hsieh, Diatchenko, Marusina, Farmer et al.: Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. ... in Proceedings of the National Academy of Sciences of the United States of America 2002 (PubMed)
    Show all 3 references for 969282

  3. Human Monoclonal MDM4-binding Protein Primary Antibody for WB - ABIN1449256 : Yang, Roe, Cliff, Williams, Ladbury, Cohen, Barford: Molecular basis for TPR domain-mediated regulation of protein phosphatase 5. in The EMBO journal 2005 (PubMed)
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  4. Human Polyclonal MDM4-binding Protein Primary Antibody for IHC, ELISA - ABIN1533176 : Shvarts, Bazuine, Dekker, Ramos, Steegenga, Merckx, van Ham, van der Houven van Oordt, van der Eb, Jochemsen: Isolation and identification of the human homolog of a new p53-binding protein, Mdmx. in Genomics 1997 (PubMed)
    Show all 2 references for 1533176

  5. Human Polyclonal MDM4-binding Protein Primary Antibody for IHC, ELISA - ABIN1532152 : Gregory, Barlow, McLay, Kaul, Swarbreck, Dunham, Scott, Howe, Woodfine, Spencer, Jones, Gillson, Searle, Zhou, Kokocinski, McDonald, Evans, Phillips, Atkinson, Cooper, Jones, Hall, Andrews, Lloyd et al.: The DNA sequence and biological annotation of human chromosome 1. ... in Nature 2006 (PubMed)
    Show all 2 references for 1532152

  6. Cow (Bovine) Polyclonal MDM4-binding Protein Primary Antibody for WB - ABIN2774604 : Gilkes, Pan, Coppola, Yeatman, Reuther, Chen: Regulation of MDMX expression by mitogenic signaling. in Molecular and cellular biology 2008 (PubMed)

更多抗MDM4-binding Protein的相互作用对抗体

Human Mdm4-binding Protein (MDM4) interaction partners

  1. These results demonstrate that cisplatin-mediated p53 (显示 TP53 抗体)(V172F) mutation regulates p53 (显示 TP53 抗体) stability at the normothermic temperature, but it is the increased recruitment of MDM4 by the homomeric or heteromeric mutant p53 (显示 TP53 抗体)(V172F) complex that inhibits p53 (显示 TP53 抗体)-dependent transactivation. This represents a novel cellular mechanism of p53 (显示 TP53 抗体) inhibition, and, thereby, induction of cisplatin resistance

  2. MDM4 protein is frequently abundant in the context of mutant p53 (显示 TP53 抗体) in basal-like breast cancer (BC) samples. MDM4 plays a critical role in the proliferation of these BC cells. MDM4 is crucial for the establishment and progression of tumours.

  3. Study used polymer statistics to estimate a global KD value for p53 (显示 TP53 抗体) binding to MdmX in the presence of the flexible linker and the intramolecular binding motif by assuming the flexible linker behaves as a wormlike chain. Calculations and measurements showed that the intramolecular binding motif reduces the apparent affinity of p53 (显示 TP53 抗体) for MdmX by a factor of 400.

  4. Data indicate that knockdown of otubain 1 (显示 OTUB1 抗体) protein (Otub1) reduced the levels of double minute 4 protein (MDMX).

  5. these data identify MDM4 as a nutrient-sensor able to inhibit mTORC1 and highlight its metabolism-related tumor-suppressing function.

  6. Data indicate that two single-nucleotide polymorphism (SNPs)rs10900598 and rs4245739, located at 3'-untranslated region (UTR (显示 UTS2R 抗体)) of double minute 4 protein (MDM4) gene, contribute to clinical outcome of advanced non-small cell lung cancer (NSCLC) patients treated with platinum-based chemotherapy.

  7. These findings suggest that Mdm2 (显示 MDM2 抗体) splice isoforms may play critical roles in the regulatory loop of p53 (显示 TP53 抗体)/Mdm2 (显示 MDM2 抗体)-Mdm4 via a RING domain-mediated biochemical mechanism.

  8. AXL (显示 AXL 抗体) overexpression or activation through growth arrest-specific 6 (Gas6 (显示 GAS6 抗体)) ligand stimulation increases MDMX and MDM2 (显示 MDM2 抗体) protein levels and decreases p53 (显示 TP53 抗体) activity.

  9. p53 (显示 TP53 抗体) stabilization, along with antagonism of its signaling partners, MDM2 (显示 MDM2 抗体) and MDMX, is a promising strategy for anticancer targeted therapy. (Review)

  10. identified a novel Her4 (显示 ERBB4 抗体)-induced posttranslational modification on MDMX

Zebrafish Mdm4-binding Protein (MDM4) interaction partners

  1. Data indicate that knockdown of the Mdm2 (显示 MDM2 抗体) and Mdm4 caused dramatic accumulation of mutant p53 protein (显示 TP53 抗体).

  2. crystal structure of N-terminal domain of Mdmx bound to 15-residue p53 (显示 TP53 抗体) peptide was determined; structure reveals that although principle features of Mdm2 (显示 MDM2 抗体)-p53 (显示 TP53 抗体) interaction are preserved, the Mdmx hydrophobic cleft on which the p53 (显示 TP53 抗体) peptide binds is altered

Mouse (Murine) Mdm4-binding Protein (MDM4) interaction partners

  1. The p53 (显示 TP53 抗体)-null mice with the highest level of Mdm4 tended to have multiple tumours. Mdm4 transgenic mice in various genetic backgrounds shows synergy in tumour development in vivo. Mdm4 may thus serve as a therapeutic target in cancers.

  2. These findings suggest that Mdm2 (显示 MDM2 抗体) splice isoforms may play critical roles in the regulatory loop of p53 (显示 TP53 抗体)/Mdm2 (显示 MDM2 抗体)-Mdm4 via a RING domain-mediated biochemical mechanism.

  3. both MDM2 (显示 MDM2 抗体) and MDMX deletion-caused pancreatic defects are completely rescued by loss of p53 (显示 TP53 抗体), verifying the crucial role of the MDM2 (显示 MDM2 抗体) and/or MDMX in regulating p53 (显示 TP53 抗体) in a spatio-temporal manner during the development, functional maintenance, and related disease progress of endocrine pancreas.

  4. we failed to detect any increase in p53 (显示 TP53 抗体) level in mutant oocytes, nor any other apoptotic marker, introgression of this targeted invalidation in p53 (显示 TP53 抗体)-/- mice restored the fertility of females. This study is the first to show that Mdm2 (显示 MDM2 抗体), but not Mdm4, has a critical role in oocyte survival and would be involved in premature ovarian insufficiency phenotype.

  5. Data show that the Mdm4-p73 (显示 ARHGAP24 抗体) axis cannot override the dominant role of p53 (显示 TP53 抗体) in development and tumorigenesis and that Mdm4 and p73 (显示 ARHGAP24 抗体) interaction during development and tumorigenesis suggests new insight into the role of p53 (显示 TP53 抗体) family members.

  6. MDM4/HIPK2 (显示 HIPK2 抗体)/p53 (显示 TP53 抗体) cytoplasmic assembly uncovers coordinated repression of molecules with anti-apoptotic activity during early DNA damage response.

  7. MDMx degradation associated with neuronal death occurs via caspase (显示 CASP3 抗体) activation in neurons, and that the progressive loss of MDMx protein represents a potential mechanism of Abeta (显示 APP 抗体)-induced neuronal death during disease progression in AD

  8. our results show MDM4-MDM2 (显示 MDM2 抗体)/p53 (显示 TP53 抗体)-IGF1R (显示 IGF1R 抗体) as an original regulatory mechanism for CNS regeneration

  9. Increased Mdm4-S mRNA levels might correlate with more aggressive cancers without encoding significant amounts of a potential oncoprotein.

  10. results reveal a novel p53 (显示 TP53 抗体)- and Mdm2 (显示 MDM2 抗体)-independent oncogenic function of Mdmx that provides new insight into the many cancers that overexpress Mdmx.

MDM4-binding Protein (MDM4) 抗原简介

Antigen Summary

This gene encodes a nuclear protein that contains a p53 binding domain at the N-terminus and a RING finger domain at the C-terminus, and shows structural similarity to p53-binding protein MDM2. Both proteins bind the p53 tumor suppressor protein and inhibit its activity, and have been shown to be overexpressed in a variety of human cancers. However, unlike MDM2 which degrades p53, this protein inhibits p53 by binding its transcriptional activation domain. This protein also interacts with MDM2 protein via the RING finger domain, and inhibits the latter's degradation. So this protein can reverse MDM2-targeted degradation of p53, while maintaining suppression of p53 transactivation and apoptotic functions. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

Alternative names and synonyms associated with MDM4-binding Protein (MDM4)

  • Mdm4 p53 binding protein homolog (mdm4) 抗体
  • Mdm4 p53 binding protein homolog (mouse) (MDM4) 抗体
  • Mdm4 p53 binding protein homolog (mouse) (Mdm4) 抗体
  • transformed 3T3 cell double minute 4 homolog (mouse) (mdm4) 抗体
  • transformed mouse 3T3 cell double minute 4 (Mdm4) 抗体
  • 4933417N07Rik 抗体
  • AA414968 抗体
  • AL023055 抗体
  • AU018793 抗体
  • AU021806 抗体
  • C85810 抗体
  • HDMX 抗体
  • Mdmx 抗体
  • MRP1 抗体
  • wu:fa09h09 抗体
  • wu:fi33d10 抗体

Protein level used designations for anti-Mdm4-binding Protein (MDM4) 抗体

double minute 4 protein , mdm2-like p53-binding protein , p53-binding protein Mdm4 , protein Mdm4 , MDM4-related protein 1 , double minute 4, human homolog of; p53-binding protein , protein Mdmx , Mdm4, transformed 3T3 cell double minute 4, p53 binding protein , double minute 4 homolog , transformed mouse 3T3 cell double minute 4

398466 Xenopus laevis
4194 Homo sapiens
478939 Canis lupus familiaris
514225 Bos taurus
304798 Rattus norvegicus
334932 Danio rerio
17248 Mus musculus
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