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Human Polyclonal CDC5L Primary Antibody für FACS, WB - ABIN652896
Grillari, Löscher, Denegri, Lee, Fortschegger, Eisenhaber, Ajuh, Lamond, Katinger, Grillari-Voglauer: Blom7alpha is a novel heterogeneous nuclear ribonucleoprotein K homology domain protein involved in pre-mRNA splicing that interacts with SNEVPrp19-Pso4. in The Journal of biological chemistry 2009
Show all 2 Pubmed References
Human Polyclonal CDC5L Primary Antibody für IF, IHC - ABIN6138265
Liu, Wang, Liu, Yu, Wang, Li, Du, Yang: Single-cell transcriptome sequencing reveals that cell division cycle 5-like protein is essential for porcine oocyte maturation. in The Journal of biological chemistry 2018
Study demonstrates that the levels of Prp19 and Cdc5L are overexpressed in hepatocellular carcinoma (HCC). Prp19 binds with Cdc5L and its downregulation results in reduction of Cdc5L. Mechanistic insights reveal that silencing Prp19 compromises translation activity of Cdc5L and facilitates lysosome-induced degradation of Cdc5L in HCC cells.
CDC5L might play an important role in glioma cell survival and disease progression.
Cdc5L was highly expressed in hepatocellular carcinoma. Overexpression of Cdc5L favors cell cycle progress of HCC cells, while downregulation of Cdc5L results in cell cycle arrest at G2/M phase and reduced cell proliferation of HCC cells.
The results show that CTNNBL1 enhances the association of CWC15 and CDC5L, both core Prp19 complex proteins and identify an overlap in the region of CDC5L that binds either CTNNBL1 or CWC15 suggesting the two proteins might exchange places in the complex.
Cdc5L is a key regulator of mitotic progression.
The N-terminal ARM-repeat domain of CTNNBL1 provides a binding site for CDC5L, a binding partner in the Prp19-CDC5L complex.
CTNNBL1 is a novel nuclear localization sequence-binding protein that recognizes RNA-splicing factors CDC5L and Prp31
Dbf4 regulates the Cdc5 Polo-like kinase through a distinct non-canonical binding interaction
A central region in hnRNP-M is required for interaction with CDC5L/PLRG1.
Blom7alpha is a novel splicing factor of the K homology domain family that might be implicated in alternative splicing by helping to position the CDC5L-SNEV(Prp19-Pso4) complex at the splice sites
CDC5 may function in pre-mRNA processing and cell cycle progression
the interaction between CDC5L and PLRG1 is essential for pre-mRNA splicing
Results indicate that CDC5L is the most likely candidate oncogene for the 6p12-p21 amplicon found in osteosarcoma.
Phosphorylation of CDC5L at threonines 411 and 438 within recognition sequences for CDKs are required for CDC5L-mediated pre-mRNA splicing.
These findings show a new function for Cdc5L in the regulation of the ATR-mediated cell-cycle checkpoint in response to genotoxic agents.
Results suggest that CDC5 may have dual roles in miRNA biogenesis: functioning as a positive transcription factor of MIR and/or acting as a component of the DICER-LIKE1 complex to enhance primary miRNA processing.
Silencing of AtCDC5 in wild-type plants all induces cell death.
These results suggest that AtCDC5 is essential for the G2/M phase transition and may regulate the function of SAM by controlling the expression of STM and WUS.
The protein encoded by this gene shares a significant similarity with Schizosaccharomyces pombe cdc5 gene product, which is a cell cycle regulator important for G2/M transition. This protein has been demonstrated to act as a positive regulator of cell cycle G2/M progression. It was also found to be an essential component of a non-snRNA spliceosome, which contains at least five additional protein factors and is required for the second catalytic step of pre-mRNA splicing.
cell division cycle 5-like protein
, CDC5 cell division cycle 5-like (S. pombe)
, CDC5 cell division cycle 5-like
, Cell division cycle 5-like protein
, cell division cycle 5-like protein-like
, cdc5-like protein
, Cdc5-related protein
, dJ319D22.1 (CDC5-like protein)
, pombe cdc5-related protein
, cell division cycle 5-related protein
, pombe Cdc5-related protein