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anti-Human DP1 Antikörper:
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Guinea Pig Polyclonal DP1 Primary Antibody für WB - ABIN6746158
David, Solimena, De Camilli: Autoimmunity in stiff-Man syndrome with breast cancer is targeted to the C-terminal region of human amphiphysin, a protein similar to the yeast proteins, Rvs167 and Rvs161. in FEBS letters 1994
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DILC may mediate the crosstalk between the cascades of IL6/STAT3 and TNFalpha signaling, indicating that DILC may act as a prognostic biomarker of sepsis, and may serve as a potential therapeutic target for the treatment of sepsis.
COMMD9 participates in TFDP1/E2F1 activation and plays a critical role in non-small cell lung cancer.
Here, the authors show that an acidic region of DP1, whose function has remained elusive, binds to the plekstrin homology (PH) domain of the p62 subunit of TFIIH that contributes to transcriptional activation.
role for E2F1 and TFDP1 in the transcriptional regulation of PITX1 in articular chondrocytes
According to our study results, the gene TFDP1 and the cell cycle pathway are strongly associated with high-grade glioblastoma multiforme (GBM); this result may provide new insights into the pathogenesis of GBM.
Amplification of CUL4A, IRS2, and TFDP1 genes showed a significant difference in disease-free survival by both univariate and multivariate survival analyses in intrahepatic cholangiocarcinoma.
The TFDP1 indel84 mutation generates a gain-of-function phenotype by increasing cell proliferation, migration, and invasion of colorectal cancer cells.
somatic mutations in DP-1 uncouple normal control of the E2F pathway, and thus define a new mechanism that could contribute to aberrant proliferation in tumor cells
The authors demonstrate that adenovirus E1A binds to E2F/DP-1 complexes through a direct interaction with DP-1 and may selectively activate a subset of E2F-regulated cellular genes during infection.
the DP-1 "Stabilon" domain was a C-terminal acidic motif and was quite important for DP-1 stability.
13q34 amplification may be of relevance in tumor progression of breast cancers by inducing overexpression of CUL4A and TFDP1, important in cell cycle regulation. These genes were also overexpressed in non-basal-like tumor samples.
TFDP1, CUL4A, and CDC16 are probable targets of an amplification mechanism and therefore may be involved, together or separately, in development and/or progression of some hepatocellular carcinomas
expression of the transcription factor DP-1 and its heterodimeric partner E2F-1 in non-Hodgkin lymphoma
TFDP1 may have a role in progression of some hepatocellular carcinomas by promoting growth of the tumor cells
DP-1alpha is a novel isoform of DP-1 that acts as a dominant-negative regulator of cell cycle progression
DP1 is a critical direct target of ARF.
SOCS-3 acts as a negative regulator of the cell cycle progression under E2F/DP-1 control by interfering with heterodimer formation between DP-1 and E2F
Kbtbd5 regulates skeletal muscle myogenesis through the regulation of E2F1-DP1 activity
Cell cycle suppression by Cdk5 is made through the formation of a previously unknown complex consisting of the p35-Cdk5 dimer and E2F1, which excludes the E2F1 cofactor, DP1, thus inhibiting E2F1 binding to the promoters of various cell cycle genes.
Absolutely required for extra-embryonic development and consequently embryonic survival.
Persistent PP2A expression prevented the appearance of the phosphorylated form of DP-1 required for cellular differentiation and reversal of dysplasia after loss of oncogene expression.
Results show that Dp1 is largely dispensable for embryonic development, despite the absolute extraembryonic requirement for Dp1.
The authors propose that these dual functions of DP1 can promote and stabilize biphasic Wnt-on and Wnt-off states in response to a gradual gradient of Wnt/beta-catenin signalling to determine differential cell fates.
This gene encodes a member of a family of transcription factors that heterodimerize with E2F proteins to enhance their DNA-binding activity and promote transcription from E2F target genes. The encoded protein functions as part of this complex to control the transcriptional activity of numerous genes involved in cell cycle progression from G1 to S phase. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 1, 15, and X.
RNA-binding protein MEX3A
, transcription factor Dp-1, like
, DRTF1-polypeptide 1
, E2F dimerization partner 1
, E2F-related transcription factor
, cell cycle regulatory transcription factor DP1
, transcription factor Dp-1
, transcription factor Dp-1 a
, transcription factor Dp-1-like