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Genetic and biochemical analyses reveal a functional interaction of MSL1 with CDK7, a subunit of the Cdk-activating kinase (CAK) complex (show CCNH ELISA Kits) of the general transcription factor TFIIH (show GTF2H5 ELISA Kits). Importantly, MSL1 depletion leads to decreased phosphorylation of Ser5 of RNA polymerase II.
CDK7 is required for the mitochondrial localization of Hid and induction of apoptosis.
The multitask protein Xpd (show ERCC2 ELISA Kits) also plays an essential role in cell cycle regulation that appears to be independent of transcription or nucleotide excision repair.
Cdk7 is required for full activation of Drosophila heat-shock genes and RNA polymerase II phosphorylation in vivo.
Expressions of components of the CAK complex (show CCNH ELISA Kits), CDK7, MAT1 (show MAT1A ELISA Kits), and Cyclin H (show CCNH ELISA Kits) are elevated in breast cancer.
MYC (show MYC ELISA Kits) promotes mRNA cap methylation and protein production of Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) signaling transcripts through recruitment of cyclin-dependent kinase 7 (CDK7) and consequently RNMT to gene promoters.
High expression of MMP14 (show MMP14 ELISA Kits) and CDK7 was independent prognostic factors for overall survival in patients with gastric cancer.
Taken together, these findings elucidated a novel mechanism of prostate cancer progression. Thus, SNHG1 might serve as a potential target for prostate cancer therapies.
Data indicate that cyclin dependent kinase 7 (CDK7) is overexpressed in gastric cancer cell lines and tissues.
Cdk7 broadly influences transcription and capping.
Our results indicated that CCNH (show CCNH ELISA Kits)/CDK7-CtBP2 (show CTBP2 ELISA Kits) axis may augment ESCC cell migration, and targeting the interaction of both may provide a novel therapeutic target of esophageal squamous cell carcinoma .
Study shows that triple-negative but not hormone receptor (show NR4A1 ELISA Kits)-positive breast cancer cells are exceptionally dependent on CDK7, a transcriptional cyclin-dependent kinase (show CDK1 ELISA Kits).
Data suggest a quantitative contribution of CDK7 to mRNA synthesis, which is critical for cellular homeostasis.
Data indicate that TG02 blocked signaling by CDKs 1, 2, 7, and 9 and ERK5 (show MAPK7 ELISA Kits), leading to potent and highly consistent antimyeloma activity.
the cyclin-dependent kinase (show CDK1 ELISA Kits) CDK7 is regulated by miR (show MLXIP ELISA Kits)-210 and is necessary for normal NP cell-cycle progression. Our findings demonstrate that miRNAs are essential for normal NP proliferation and cell-cycle progress during neocortical development
Inhibition of CDK7 bypasses spindle assembly checkpoint via premature cyclin B degradation during oocyte meiosis.
Whereas Cdk7 was completely dispensable for global transcription, it was essential for the cell cycle via phosphorylation of Cdk1 (show CDK1 ELISA Kits) and Cdk2 (show CDK2 ELISA Kits). In vivo, Cdk7 was indispensable for cell proliferation except during the first stages of embryonic development.
investigated the function of the Cdk7.cyclin (show PCNA ELISA Kits) H.Mat1 complex in murine embryonic stem (ES) cells and preimplantation embryos to determine whether it regulates the unique cell cycle structure and transcriptional network of pluripotent cells
Cdk7 kinase activity and cell cycle kinetics were found to be comparable in wild-type and Hint(-/-) mouse embryonic fibroblasts, suggesting that Hint may not be a key regulator of Cdk7 activity
results demonstrate that the Cdk7 submodule of transcription factor IIH acts as a physiological roadblock to adipogenesis by inhibiting PPARgamma (show PPARG ELISA Kits) activity
Inhibition of SF-1 (show SF1 ELISA Kits)-mediated transcription by SUMOylation in adrenocortical cancer cells is mediated through reduced CDK7-induced phosphorylation of SF-1 (show SF1 ELISA Kits).
CDK7 and CCNH (show CCNH ELISA Kits) activate CDC2 (show CDK1 ELISA Kits) by T161 phosphorylation and make up CDK-activating kinase, which is required for normal meiotic progression during porcine oocyte maturation.
The present results suggest that demecolcine might contribute to the activation of the Mos (show MOCOS ELISA Kits)/MAPK (show MAPK1 ELISA Kits) pathway and affect spindle structure
Analysis of Cdk7 expression in unfertilized eggs, embryos and organs of adult zebrafish suggests that Cdk7 message is maternally loaded; its transcript is detected throughout early embryonic development.
The protein encoded by this gene is a member of the cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of Saccharomyces cerevisiae cdc28, and Schizosaccharomyces pombe cdc2, and are known to be important regulators of cell cycle progression. This protein forms a trimeric complex with cyclin H and MAT1, which functions as a Cdk-activating kinase (CAK). It is an essential component of the transcription factor TFIIH, that is involved in transcription initiation and DNA repair. This protein is thought to serve as a direct link between the regulation of transcription and the cell cycle.
, cyclin-dependent kinase 7 (MO15 homolog, Xenopus laevis, cdk-activating kinase)
, cyclin-dependent kinase 7 (MO15, cdk-activating kinase)
, 39 KDa protein kinase
, CDK-activating kinase 1
, TFIIH basal transcription factor complex kinase subunit
, cell division protein kinase 7
, homolog of Xenopus MO15 Cdk-activating kinase
, kinase subunit of CAK
, p39 Mo15
, protein kinase
, serine/threonine kinase stk1
, serine/threonine protein kinase 1
, serine/threonine protein kinase MO15
, serine/threonine-protein kinase 1
, 39 protein kinase
, P39 Mo15
, cyclin-dependent kinase 7 (MO15 homolog Xenopus laevis cdk-activating kinase)
, cyclin-dependent kinase 7 (homolog of Xenopus MO15 cdk-activating kinase)
, 39 kDa protein kinase
, CDK-activating kinase
, CR4 protein kinase
, CRK4 PK (CDC2-related-kinase-4 protein kinase)
, protein-tyrosine kinase MPK-7
, 40 kDa protein kinase
, CDC2/CDK2,4-activating kinase
, P40 MO15
, cell division protein kinase 7-like protein
, Moloney murine sarcoma viral (v-mos) oncogene homolog
, oocyte maturation factor Mos