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Core component of the DBIRD complex, a multiprotein complex that acts at the interface between core mRNP particles and RNA polymerase II (RNAPII) and integrates transcript elongation affects local transcript elongation rates and alternative splicing of a large set of exons embedded in (A + T)-rich DNA regions. De plus, nous expédions CCAR2 Protéines (4) et beaucoup plus de produits pour cette protéine.
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CCAR2/DBC1 inhibits recombination by limiting the initiation and the extent of DNA end resection, thereby acting as an antagonist of CtIP (Montrer RBBP8 Anticorps).
conclude, these findings demonstrated that DBC1 was essential in tumorigenesis and proliferation. Moreover, it was identified as a potential therapeutic target for HCC (Montrer FAM126A Anticorps).
Long non-coding RNA MALAT1 interacts with DBC1 to regulate p53 (Montrer TP53 Anticorps) acetylation.
Data suggest that DBC1 has a dual function in regulating beta-catenin (Montrer CTNNB1 Anticorps)-PROX1 (Montrer PROX1 Anticorps) signaling axis: as a coactivator for both beta-catenin (Montrer CTNNB1 Anticorps) and PROX1 (Montrer PROX1 Anticorps).
important role for CCAR2 in maintaining cell cycle progression and promoting squamous cell carcinoma (SCC (Montrer CYP11A1 Anticorps)) tumorigenesis.
Data show that the interaction between cell cycle and apoptosis regulator 2 (CCAR2) and heat shock protein 60 (Hsp60 (Montrer HSPD1 Anticorps)) increases in the presence of rotenone.
Results found transcriptional levels of DBC1,a negative regulator of HDAC3 (Montrer HDAC3 Anticorps) significantly reduced in type 2 diabetes mellitus patients.
DBC1 protein could be a prognostic marker of shorter recurrence-free survival in hepatocellular carcinoma patients after hepatectomy and human hepatocarcinogenesis was a multistep process accompanied by a stepwise increase in high DBC1 expression from low-grade dysplastic nodules, through high-grade dysplastic nodules, to hepatocellular carcinoma.
Results suggest that DBC1 is integral to the maintenance of the circadian molecular clock.
loss of DBC1 expression plays a role in tumorigenesis and tumor progression in gallbladder carcinoma.
Dbc1 ablation increases Scd1 (Montrer SCD Anticorps) levels, causes obesity and insulin (Montrer INS Anticorps) resistance.
phosphorylation of DBC1 at its C terminus by IKKalpha (Montrer CHUK Anticorps) facilitates its interaction with RelB (Montrer RELB Anticorps) and IKKalpha (Montrer CHUK Anticorps), indicating that DBC1-mediated suppression of alternative NF-kappaB (Montrer NFKB1 Anticorps) is regulated by IKKalpha (Montrer CHUK Anticorps).
induced the expression of nuclear factor kappa B (NF-kappaB (Montrer NFKB1 Anticorps))-regulated inflammatory cytokines in fully differentiated 3T3-L1 adipocytes, possibly through the inhibition of Sirt1 (Montrer SIRT1 Anticorps) activity
We propose that DBC1 is part of the molecular machinery that regulates fat storage capacity in adipocytes and participates in the "turn-off" switch that limits adipocyte fat accumulation.
DBC1 as a novel regulator of gluconeogenesis.
HDAC3 is negatively regulated by the nuclear protein DBC1
New role for DBC1 as an in vivo regulator of SIRT1 (Montrer SIRT1 Anticorps) activity and liver steatosis, in which interaction with SIRT1 (Montrer SIRT1 Anticorps) may serve as a new target for therapies aimed at nonalcoholic liver steatosis.
Core component of the DBIRD complex, a multiprotein complex that acts at the interface between core mRNP particles and RNA polymerase II (RNAPII) and integrates transcript elongation affects local transcript elongation rates and alternative splicing of a large set of exons embedded in (A + T)-rich DNA regions. Inhibits SIRT1 deacetylase activity leading to increasing levels of p53/TP53 acetylation and p53-mediated apoptosis. Inhibits SUV39H1 methyltransferase activity.
DBIRD complex subunit KIAA1967
, deleted in breast cancer 1
, p30 DBC protein
, DBIRD complex subunit KIAA1967 homolog
, cell cycle and apoptosis regulator protein 2