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BRD7 encodes a protein which is a member of the bromodomain-containing protein family. Zusätzlich bieten wir Ihnen BRD7 Proteine (6) und BRD7 Kits (1) und viele weitere Produktgruppen zu diesem Protein an.
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Dog (Canine) Polyclonal BRD7 Primary Antibody für IHC, WB - ABIN2780896
Zhou, Tan, Hershenson: Yersinia YopJ inhibits pro-inflammatory molecule expression in human bronchial epithelial cells. in Respiratory physiology & neurobiology 2004
Show all 2 Pubmed References
our data indicated that BRD7 may serve as a tumor suppressor in hepatocellular carcinoma
Results demonstrate a novel function of BRD7 in TGF-beta (zeige TGFB1 Antikörper) signaling. BRD7 interacts with the Smad (zeige SMAD1 Antikörper) 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.
Overexpression of BRD7 inhibited cyclin D and myc (zeige MYC Antikörper) expression. Our findings are consistent with a tumor suppressor role for BRD7 in lung adenocarcinoma tumorigenesis.
the expression of miR (zeige MLXIP Antikörper)-141 in BRD7-overexpressing NPC (zeige NPC1 Antikörper) cells could partially reverse the tumor suppressive effect of BRD7 on cell proliferation and tumor growth in vitro and in vivo.
constructed a regulating network of BRD7 downstream genes, and this network suggests multiple feedback regulations of the pathways. Furthermore, we validated BIRC2 (zeige BIRC2 Antikörper), BIRC3 (zeige BIRC3 Antikörper), TXN2 (zeige TXN2 Antikörper), and NOTCH1 (zeige NOTCH1 Antikörper) genes as direct, functional BRD7 targets
Propose that the balance between BRD7 function and Ras/Raf (zeige RAF1 Antikörper)/MEK (zeige MAP2K1 Antikörper)/ERK (zeige EPHB2 Antikörper) activity is important for determining the outcomes of HCV infection and HCC (zeige FAM126A Antikörper) development.
Ectopic expression of BRD7 could significantly inhibit miR (zeige MLXIP Antikörper)-300-promoted proliferation, invasion and epithelial-mesenchymal transition in osteosarcoma.
BRD7 promoter hypermethylation is an indicator of well differentiated oral squamous cell carcinomas.
Data indicate that bromodomain-containing protein 7 (BRD7) was a direct target of microRNA-410 (miR (zeige MLXIP Antikörper)-410).
lower BRD7 expression is an indicator for poor prognosis in patients with osteosarcoma.
Furthermore, Brd7 inhibition alters the phenotype of macrophages and promotes plaque instability, at least partly via STAT6 (zeige STAT6 Antikörper) signaling. Our data define a previously undescribed role of Brd7 in the development of atherosclerosis.
Homozygous BRD7 knockout (KO) mice showed retardation in development.
Homozygous knockout of BRD7 (BRD7(-/-)) resulted in complete male infertility and spermatogenesis defects, including deformed acrosomal formation, degenerative elongating spermatids and irregular head morphology in postmeiotic germ cells in the seminiferous epithelium, which led to the complete arrest of spermatogenesis at step 13.
Results link BRD7 to medial prefrontal cortex synaptic plasticity regulation; knockout leads to impaired cognitive behavior accompanied by reduced synaptic related proteins expression and dendritic spines or branching in the medial prefrontal cortex
BRD7 interacts with the regulatory subunits of phosphatidylinositol 3-kinase (PI3K) and increases the nuclear translocation of both p85alpha and p85beta and the spliced form of XBP1 (zeige XBP1 Antikörper) (XBP1s).
TRIM24 (zeige TRIM24 Antikörper) regulates AR-mediated transcription in collaboration with TIP60 (zeige KAT5 Antikörper) and BRD7.
BRD7 is a novel PBAF-specific SWI (zeige SMARCA1 Antikörper)/SNF (zeige SNRPA Antikörper) subunit that is required for target gene activation and repression in embryonic stem cells
This gene encodes a protein which is a member of the bromodomain-containing protein family. The product of this gene has been identified as a component of one form of the SWI/SNF chromatin remodeling complex, and as a protein which interacts with p53 and is required for p53-dependent oncogene-induced senescence which prevents tumor growth. Pseudogenes have been described on chromosomes 2, 3, 6, 13 and 14. Alternative splicing results in multiple transcript variants.
bromodomain containing 7
, nuclear transcriptor-like protein
, bromodomain-containing protein 7-like
, bromodomain-containing protein 7
, 75 kDa bromodomain protein
, protein CELTIX-1
, bromodomain protein 75 kDa
, bromodomain-containing 7
, protein tyrosine phosphatase, non-receptor type 13 interacting protein