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The protein encoded by MDC1 contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence.
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Human Polyclonal MDC1 Primary Antibody for ICC, IF - ABIN151859
Shi, Ma, Willers, Akhtar, Scott, Zhang, Powell, Zhang: Disassembly of MDC1 foci is controlled by ubiquitin-proteasome-dependent degradation. in The Journal of biological chemistry 2008
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Human Polyclonal MDC1 Primary Antibody for IF, WB - ABIN2475546
Dranove, Shanley, White: How fast are hospital prices really rising? in Medical care 1991
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Human Polyclonal MDC1 Primary Antibody for ICC, IF - ABIN4333285
Mastrocola, Kim, Trinh, Rodenkirch, Tibbetts: The RNA-binding protein fused in sarcoma (FUS) functions downstream of poly(ADP-ribose) polymerase (PARP) in response to DNA damage. in The Journal of biological chemistry 2013
Human Polyclonal MDC1 Primary Antibody for ICC, IF - ABIN151861
Mallette, Mattiroli, Cui, Young, Hendzel, Mer, Sixma, Richard: RNF8- and RNF168-dependent degradation of KDM4A/JMJD2A triggers 53BP1 recruitment to DNA damage sites. in The EMBO journal 2012
Human Polyclonal MDC1 Primary Antibody for IHC (p), IP - ABIN151860
Floyd, Pacold, Huang, Clarke, Lam, Cannell, Bryson, Rameseder, Lee, Blake, Fydrych, Ho, Greenberger, Chen, Maffa, Del Rosario, Root, Carpenter, Hahn, Sabatini, Chen, White, Bradner, Yaffe: The bromodomain protein Brd4 insulates chromatin from DNA damage signalling. in Nature 2013
MDC1 plays a fundamentally significant role in maintenance of genomic stability through a DNA damage response-independent pathway.
MDC1 silencing enhances the radiosensitivity of human nasopharyngeal cancer CNE1 cells and results in xenograft tumor growth inhibition.
oligomerization of MDC1 plays an important role in DDR (显示 DDR1 抗体) and help understand the formation of proteins complexes at the sites of DNA damage.
structural insight into MDC1-CHK2 (显示 CHEK2 抗体) interaction
the DNA damage response pathway centered on MDC1 triggers epigenetic silencing of sex chromosomes in germ cells
Data show that loss of Mof (显示 KAT8 抗体) leads to reduction of histone H4 (显示 HIST1H4H 抗体) K16 (显示 KRT16 抗体) acetylation, cell cycle arrest, chromosome aberration, defects in DNA damage repair, and complete loss of Mdc1 response to DNA damage.
Data show that ATM (显示 ATM 抗体)-dependent resection at a subset of DSBs leads to ATR (显示 ATR 抗体)-dependent Chk1 (显示 CHEK1 抗体) activation, and that 53BP1 (显示 TP53BP1 抗体)(-/-) and MDC1(-/-) cells manifest a checkpoint defect at high radiation doses.
identification and description of a functional homologue of human MDC1/ NFBD1; in response to ionizing radiation it forms foci that co-localize with the MRE11 (显示 MRE11A 抗体)-RAD50 (显示 RAD50 抗体)-NBS1 (显示 NBN 抗体) (MRN) complex and factors such as gammaH2AX (显示 H2AFX 抗体) and 53BP1 (显示 TP53BP1 抗体)
MDC1, as a signal amplifier of the ATM (显示 ATM 抗体) pathway, is vital in controlling proper DNA damage response and maintaining genomic stability.
MDC1 knockdown affected the formation of telomere dysfunction-induced foci.
ASF1a (显示 ASF1A 抗体) promotes non-homologous end joining repair by facilitating phosphorylation of MDC1 by ATM (显示 ATM 抗体) at double-strand breaks.
the opposing activities of RNF4 (显示 RNF4 抗体) and ataxin-3 (显示 ATXN3 抗体) consolidate robust MDC1-dependent signaling and repair ofDNA double-strand break.
NFBD1 protein is overexpressed in NPC (显示 NPC1 抗体) tissues and that silencing NFBD1 can inhibit cell growth, induce apoptosis, increase the production of intracellular ROS (显示 ROS1 抗体). NFBD1 knockdown also inhibits the tumorigenicity of NPC (显示 NPC1 抗体) cells in vivo.
NFBD1 knockdown improves the chemosensitivity of NPC (显示 NPC1 抗体) cells by inhibiting cell growth and promoting apoptosis through the impairment of DNA damage repair, suggesting NFBD1 as a novel therapeutic target for NPC (显示 NPC1 抗体).
knockdown of MCM2 or MCM6 could significantly inhibit foci forming of MDC1 in TE-1 nuclei in response to bleomycin-induced DNA damage (p < 0.001). This study indicates the direct interaction between MDC1 and MCMs in TE-1 nuclei.
The interaction of MDC1 with RNF8 (显示 RNF8 抗体), but not with ATM (显示 ATM 抗体) requires WRAP53beta, suggesting that WRAP53beta facilitates the former interaction without altering phosphorylation of MDC1 by ATM (显示 ATM 抗体).
MDC1 recruits TNKS1 (显示 TNKS 抗体) and TNKS2 (显示 TNKS2 抗体) to DNA lesions.
we generated two HEP (显示 EPHB6 抗体)-2 cell lines with a stable knockdown of MDC1 or 53BP1 (显示 TP53BP1 抗体) with short hairpin RNA (shRNA), respectively, and investigated the effect of MDC1 and 53BP1 (显示 TP53BP1 抗体) on cell radiosensitivity
During replicative senescence and stress-induced premature senescence, MDC1 is downregulated by upregulating miR (显示 MLXIP 抗体)-22.
The protein encoded by this gene contains an N-terminal forkhead domain, two BRCA1 C-terminal (BRCT) motifs and a central domain with 13 repetitions of an approximately 41-amino acid sequence. The encoded protein is required to activate the intra-S phase and G2/M phase cell cycle checkpoints in response to DNA damage. This nuclear protein interacts with phosphorylated histone H2AX near sites of DNA double-strand breaks through its BRCT motifs, and facilitates recruitment of the ATM kinase and meiotic recombination 11 protein complex to DNA damage foci.
mediation of DNA damage checkpoint 1
, mediator of DNA damage checkpoint protein 1
, homologue to Drosophila photoreceptor protein calphotin
, mediator of DNA damage checkpoint 1
, nuclear factor with BRCT domains 1