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The protein encoded by RAD17 is highly similar to the gene product of Schizosaccharomyces pombe rad17, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. Zusätzlich bieten wir Ihnen RAD17 Homolog (S. Pombe) Proteine (4) und RAD17 Homolog (S. Pombe) Kits (3) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 184 products:
Human Polyclonal RAD17 Primary Antibody für FACS, WB - ABIN151253
Li, Peterson, Kanter-Smoler, Wei, Ramagli, Sunnerhagen, Siciliano, Legerski: hRAD17, a structural homolog of the Schizosaccharomyces pombe RAD17 cell cycle checkpoint gene, stimulates p53 accumulation. in Oncogene 1999
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Human Polyclonal RAD17 Primary Antibody für ICC, IF - ABIN4349066
Kato, Nicholson, Neiman, Rantalainen, Holmes, Barrett, Uhlén, Nilsson, Spector, Schwenk: Variance decomposition of protein profiles from antibody arrays using a longitudinal twin model. in Proteome science 2011
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Human Polyclonal RAD17 Primary Antibody für PLA, WB - ABIN151740
Jones, Colnaghi, Huang: Dysregulation of DNA polymerase κ recruitment to replication forks results in genomic instability. in The EMBO journal 2012
Human Polyclonal RAD17 Primary Antibody für PLA, WB - ABIN151741
Ge, Jackson, Blow: Dormant origins licensed by excess Mcm2-7 are required for human cells to survive replicative stress. in Genes & development 2007
Cow (Bovine) Polyclonal RAD17 Primary Antibody für WB - ABIN2779300
Tsao, Geisen, Abraham: Interaction between human MCM7 and Rad17 proteins is required for replication checkpoint signaling. in The EMBO journal 2004
a mutant Rad17 pathway is associated with a general deregulation of DNA repair, which seems to be correlated with a deficiency in non-homologous double strand break repair.
The Rad17 C-terminal tail is a molecular switch that regulates the 9-1-1 interaction and the ATR pathway.
These data indicate that the interaction with the 9-1-1 complex is not required for Rad17 protein to be an efficient substrate for the UV-induced phosphorylation. Our data also raise the possibility that the 9-1-1 complex plays a negative regulatory role in the Rad17 phosphorylation. We also show that the nucleotide-binding activity of Rad17 is required for its nuclear localization.
In a Japanese population, the variant allele of hRAD17 is significantly associated with a decreased risk of Colorectal Cancer among light smokers and rectal cancer patients and with an increased risk of Colorectal Cancer among heavy smokers.
Authors show that BRCA1 and RAD17 genes, whose derived proteins play a pivotal role in DNA damage repair, are transcriptional targets of gain-of-function mutant p53 (zeige TP53 Antikörper) proteins.
USP20 (zeige USP20 Antikörper) and Rad17 interact, and that this interaction is enhanced by UV exposure. We show that USP20 (zeige USP20 Antikörper) regulation of Rad17 is at the protein level in a proteasome-dependent manner. USP20 (zeige USP20 Antikörper) depletion results in poor activation of Chk1 (zeige CHEK1 Antikörper) protein by phosphorylation
These data suggest that v-Src (zeige SRC Antikörper) attenuates ATR (zeige ANTXR1 Antikörper)-Chk1 (zeige CHEK1 Antikörper) signaling through the inhibition of Rad17-Rad9 (zeige RAD9A Antikörper) interaction.
Rad17 is phosphorylated by ATM (zeige ATM Antikörper) at Thr622 resulting in a direct interaction of Rad17 with NBS1 (zeige NBN Antikörper), facilitating recruitment of MRE11 (zeige MRE11A Antikörper), RAD50 (zeige RAD50 Antikörper) and ATM (zeige ATM Antikörper) to the DNA double-strand breaks.
Our data suggest RAD17 as a novel target protein for gemcitabine combination therapy supplementing or complementing inhibition of CHK1 (zeige CHEK1 Antikörper).
Knockdown of Rad17 with two independent siRNAs significantly reduced Chk1 (zeige CHEK1 Antikörper) phosphorylation and substantial RPA32 (zeige RPA2 Antikörper) Ser33 phosphorylation.
Data indicate that regulation of Rad17 turnover is through the Cdh1 (zeige CDH1 Antikörper)/anaphase-promoting complex pathway in breast cancer cells.
targeted deletion of an N-terminal part of mRad17, the mouse homolog of the Schizosaccharomyces pombe Rad17 checkpoint clamp-loader component, resulted in embryonic lethality during early/mid-gestation
The protein encoded by this gene is highly similar to the gene product of Schizosaccharomyces pombe rad17, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. This protein shares strong similarity with DNA replication factor C (RFC), and can form a complex with RFCs. This protein binds to chromatin prior to DNA damage and is phosphorylated by the checkpoint kinase ATR following damage. This protein recruits the RAD1-RAD9-HUS1 checkpoint protein complex onto chromatin after DNA damage, which may be required for its phosphorylation. The phosphorylation of this protein is required for the DNA-damage-induced cell cycle G2 arrest, and is thought to be a critical early event during checkpoint signaling in DNA-damaged cells. Eight alternatively spliced transcript variants of this gene, which encode four distinct proteins, have been reported. Two pseudogenes, located on chromosomes 7 and 13, have been identified.
RAD17 homolog (S. pombe)
, cell cycle checkpoint protein RAD17-like
, cell cycle checkpoint protein RAD17
, Checkpoint protein, involved in the activation of the DNA damage and meiotic pachytene checkpoints; with Mec3p and Ddc1p, forms a clamp that is loaded onto partial duplex DNA; homolog of human and S. pombe Rad1 and U. maydis Rec1 proteins
, RAD17 homolog
, Cell cycle checkpoint protein RAD17
, RAD1 homolog
, RF-C activator 1 homolog
, RF-C/activator 1 homolog
, Rad17-like protein
, cell cycle checkpoint protein (RAD17)