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This MCM4 mutation affected human MCM4/6/7 complex formation, since the complex containing the mutant MCM4 protein is unstable and the mutant MCM4 protein is tend to be degraded.
We did not find any evidence of augmented response to a short-term (48 h) cisplatin treatment in these MCM4-deficient cells. However, MCM4-/HPV16+ SiHa cells cannot withstand a prolonged treatment (up to 5 days) of even a sublethal dosage of cisplatin
Purified MCM4/6/7 complex containing the G364R MCM4 exhibited similar levels of single-stranded DNA binding and ATPase (show DNAH8 ELISA Kits) activities to the complex containing wild-type MCM4
Mutant p53 (show TP53 ELISA Kits) depletion profoundly influenced PARP1 (show PARP1 ELISA Kits) localization and increased the level of PCNA (show PCNA ELISA Kits) and MCM4 proteins.
Of the total, the deregulation of several genes (CDK1 (show CDK1 ELISA Kits), CDK2 (show CDK2 ELISA Kits), CDK4 (show CDK4 ELISA Kits), MCM2 (show MCM2 ELISA Kits), MCM3 (show MCM3 ELISA Kits), MCM4, EIF3a (show EIF6 ELISA Kits) and RPN2 (show PSMD1 ELISA Kits)) were potentially associated with disease development and progression.
Mcm2-7 (show MCM2 ELISA Kits) loads onto origins during initiation as a double hexamer, yet does not act as a double-stranded DNA pump during elongation.
Peroxisome proliferator-activated receptor gamma (show PPARG ELISA Kits) coactivator 1beta (PGC-1beta (show PPARGC1B ELISA Kits)) protein attenuates vascular lesion formation by inhibition of chromatin loading of minichromosome maintenance complex in smooth muscle cells
point mutation of MCM4 perturbs proper interaction with MCM6 (show MCM6 ELISA Kits) to affect complex formation of MCM4/6/7 that is a core structure of MCM2-7 (show MCM2 ELISA Kits) complex
Mutations in MCM4/PRKDC (show PRKDC ELISA Kits) represent a novel cause of DNA breakage and NK cell deficiency.
Widdrol breaks DNA directly in HT29 cells, resulting in checkpoint activation via Chk2 (show CHEK2 ELISA Kits)-p53 (show TP53 ELISA Kits)-Cdc25A (show CDC25A ELISA Kits)-p21 (show CDKN1A ELISA Kits)-MCM4 pathway and finally cells go to G1-phase cell cycle arrest and apoptosis.
Together, these data support a model in which chromosomal abnormalities in Sdl mice result from the ability of MCM4(D573H) to incorporate into MCM complexes and render them inactive.
partial MCM4 deficiency results in a genetic syndrome of growth retardation with adrenal insufficiency and selective NK deficiency
MCM4 mutation may have a role in adrenal failure, short stature, and natural killer cell deficiency
role of subunits in DNA helicase acdtivity
Substrate preference and helicase (show DNA2 ELISA Kits) actions of mouse MCM4/6/7 helicase (show DNA2 ELISA Kits) complexes.
MCM4 phosphorylation by Cdc7 kinase facilitates its interaction with Cdc45 on chromatin
Hypomorphic alleles of Mcm4 may increase breast cancer risk.
Loss of one allele of cdc2l (show CDK13 ELISA Kits) genefacilitates carcinogen-induced skin carcinogenesis in vivo.
Mcm4(Chaos3) mutation appears to destabilize the MCM2-7 (show MCM2 ELISA Kits) complex, causing impaired DNA replication and may have a causative role in cancer development.
The protein encoded by this gene is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 6 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of this protein by CDC2 kinase reduces the DNA helicase activity and chromatin binding of the MCM complex. This gene is mapped to a region on the chromosome 8 head-to-head next to the PRKDC/DNA-PK, a DNA-activated protein kinase involved in the repair of DNA double-strand breaks. Alternatively spliced transcript variants encoding the same protein have been reported.
DNA replication licensing factor mcm4
, MCM4 minichromosome maintenance deficient 4
, minichromosome maintenance protein 4
, DNA replication licensing factor MCM4
, CDC21 homolog
, homolog of S. pombe cell devision cycle 21
, minichromosome maintenance deficient 4
, mini chromosome maintenance deficient 4 homolog
, minichromosome maintenance deficient 4 homolog