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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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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.
Proteosome-mediated degradation and poly-ubiquitination of AR were increased with the knock-down of DBC1.
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