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Lead Time
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Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Acts both as coactivator and as corepressor. May play a role in chromatin remodeling. Activator of the Wnt signaling pathway in a DVL1-dependent manner by negatively regulating the GSK3B phosphotransferase activity. Induces dephosphorylation of GSK3B at 'Tyr-216'. Down-regulates TRIM24-mediated activation of transcriptional activation by AR. Transcriptional corepressor that down-regulates the expression of target genes. Binds to target promoters, leading to increased histone H3 acetylation at 'Lys-9' (H3K9ac). Binds to the ESR1 promoter. Recruits BRCA1 and POU2F1 to the ESR1 promoter. Coactivator for TP53-mediated activation of transcription of a set of target genes. Required for TP53-mediated cell-cycle arrest in response to oncogene activation. Promotes acetylation of TP53 at 'Lys-382', and thereby promotes efficient recruitment of TP53 to target promoters. Inhibits cell cycle progression from G1 to S phase.
Gene References into Functions
the transcriptional signature of low BRD7 expressing cells is associated with increased angiogenesis.PMID:28951988
our data indicated that BRD7 may serve as a tumor suppressor in hepatocellular carcinomaPMID:26919247
Results demonstrate a novel function of BRD7 in TGF-beta signaling. BRD7 interacts with the Smad tumor suppressor complex, and enhances both DNA-binding ability and transcriptional activity of Smads. BRD7 functions in growth inhibition and tumor suppression partly as a transcriptional co-activator of Smads.PMID:27270427
Overexpression of BRD7 inhibited cyclin D and myc expression. Our findings are consistent with a tumor suppressor role for BRD7 in lung adenocarcinoma tumorigenesis.PMID:27580131
the expression of miR-141 in BRD7-overexpressing NPC cells could partially reverse the tumor suppressive effect of BRD7 on cell proliferation and tumor growth in vitro and in vivo.PMID:27010857
constructed a regulating network of BRD7 downstream genes, and this network suggests multiple feedback regulations of the pathways. Furthermore, we validated BIRC2, BIRC3, TXN2, and NOTCH1 genes as direct, functional BRD7 targetsPMID:26407966
Propose that the balance between BRD7 function and Ras/Raf/MEK/ERK activity is important for determining the outcomes of HCV infection and HCC development.PMID:26620707
Ectopic expression of BRD7 could significantly inhibit miR-300-promoted proliferation, invasion and epithelial-mesenchymal transition in osteosarcoma.PMID:26010572
BRD7 promoter hypermethylation is an indicator of well differentiated oral squamous cell carcinomas.PMID:25743841
Data indicate that bromodomain-containing protein 7 (BRD7) was a direct target of microRNA-410 (miR-410).PMID:26149213
lower BRD7 expression is an indicator for poor prognosis in patients with osteosarcoma.PMID:24840027
These results suggested that BRD7 acts as a tumor suppressor in epithelial ovarian cancersPMID:24198243
Disturbing miR-182 and -381 inhibits BRD7 transcription and glioma growth by directly targeting LRRC4.PMID:24404152
BRD7-mediated translocation of a subfraction (but not all) of the p85 protein to the nucleus could enhance PI3K signaling.PMID:24657164
No evidence for breast cancer susceptibility is associated with variants of BRD7.PMID:22864638
Data show a substantial proportion of germ-line mutations in triple-negative breast cancer (TNBC), with a preponderance of BRCA1 mutations over mutations in BRCA2 or PALB2, but no evidence to implicate BRD7 mutations in the etiology of TNBC.PMID:23110154
The region from aa219 to aa450 is primarily defined as an atypical nuclear export signal in BRD7.PMID:21873788
Data indicate that BRD7 may be related to the occurrence, development, and metastasis of lung cancers.PMID:22008115
miR-200c inhibits the expression of BRD7. MiR-200c regulated the translocation of beta-catenin from the cytoplasm to the nucleus via inhibition of BRD7, resulting in increased expression of its transcriptional target genes, cyclinD1 and c-myc.PMID:22015043
as unique regulators of replicative senescence in human cells, both BRD7 and BAF180 regulate p53 transcriptional activity toward a subset of its target genes required for replicative and oncogenic stress senescence inductionPMID:20660729
BRD7 suppresses tumorigenicity by serving as a p53 cofactor required for the efficient induction of p53-dependent oncogene-induced senescence.PMID:20228809
Regulation of transcription by E1B-AP5 is mediated by complex formation with this protein.PMID:12489984
BRD7 could up-regulate the expression levels of BRD2 and BRD3 genes in mRNA level to some extent.PMID:12600283
Expression levels of NAG-7, and BRD7 did not alter in gastric and colorectal cancers. NAG-7 and BRD7 genes may not play role in gastric and colorectal carcinogenesis.PMID:12918109
BRD7 inhibits G1-S progression by transcriptionally regulating some important molecules involved in ras/MEK/ERK and Rb/E2F pathways.PMID:15137061
Taken together, the present work shed light on the fact that a novel bromodomain gene, BRD7, is of importance in transcriptional regulation and cellular events including cell cycle.PMID:16265664
the nuclear localization of BRD7 is critical for the expression of cell cycle related molecules and cell biological function.PMID:16475162
The results showed that BRD7 could interact with BRD2 and the region from amino acid 430 to 798 of BRD2 was critical for the interaction of BRD2 with BRD7. BRD2 mainly localizes in nucleus and BRD2 has distinct roles in initiating apoptosis.PMID:16786191
BRD7 promoter demethylation is a prerequisite for high level induction of BRD7 gene expression in human nasopharyngeal carcinoma cellsPMID:18778484
BRD7 is a novel PBAF-specific SWI/SNF subunit that is required for target gene activation and repression in embryonic stem cellsPMID:18809673