Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Wählen Sie die Spezies und Applikation aus
anti-Human CDT1 Antikörper:
anti-Mouse (Murine) CDT1 Antikörper:
anti-Rat (Rattus) CDT1 Antikörper:
Sie gelangen zu unserer vorgefilterten Suche.
Human Polyclonal CDT1 Primary Antibody für ICC, IF - ABIN251007
Pos, Wiener, Pocza, Racz, Toth, Darvas, Molnar, Hegyesi, Falus: Histamine suppresses fibulin-5 and insulin-like growth factor-II receptor expression in melanoma. in Cancer research 2008
Show all 4 Pubmed References
Human Polyclonal CDT1 Primary Antibody für ELISA, WB - ABIN249645
Whittaker, Royzman, Orr-Weaver et al.: Drosophila double parked: a conserved, essential replication protein that colocalizes with the origin recognition complex and links DNA replication with mitosis and the down-regulation of S phase ... in Genes & development 2000
Human Monoclonal CDT1 Primary Antibody für WB - ABIN2668790
Arentson, Faloon, Seo, Moon, Studts, Fremont, Choi: Oncogenic potential of the DNA replication licensing protein CDT1. in Oncogene 2002
DTL (zeige DTL Antikörper) promotes genomic stability through two distinct mechanisms. First, it is an essential component of the CUL4-DDB1 complex that controls CDT1 levels, thereby preventing rereplication. Second, it is required for the early G2/M checkpoint.
PPP2R3B (zeige PPP2R3B Antikörper) codes for the PR70 protein, a regulatory substrate-recognizing subunit of protein phosphatase 2A. PR70 decreased melanoma growth by negatively interfering with DNA replication and cell cycle progression through its role in stabilizing CDC6 (zeige CDC6 Antikörper)-chromatin licensing and CDT1 interaction
USP37 (zeige USP37 Antikörper) interacts with Cdt1 and is able to de-ubiquitinate Cdt1 in vivo and, USP37 (zeige USP37 Antikörper) is able to regulate the loading of MCM complexes onto the chromatin.
mismatch repair (MMR (zeige MRC1 Antikörper)) proteins are also involved in the degradation of Cdt1 after ultraviolet irradiation in the G1 phase
Cdt1-binding protein GRWD1 promotes chromatin fluidity by influencing nucleosome structures, e.g., by transient eviction of H2A-H2B, and thereby promotes efficient MCM loading at replication origins.
ATM (zeige ATM Antikörper) silencing induced partial reduction in levels of Skp2, a component of SCF (zeige KITLG Antikörper)(Skp2) ubiquitin ligase that controls Cdt1 degradation.
FBXO31 (zeige FBXO5 Antikörper) interacts with Cdt1 and regulates the degradation of Cdt1 in G2 phase.
Protein levels of Geminin (zeige GMNN Antikörper) and Cdt1 are tightly regulated through the cell cycle, and the Cdt1-Geminin (zeige GMNN Antikörper) complex likely acts as a molecular switch that can enable or disable the firing of each origin of replication.
These results demonstrate an important role for Cdt1 in human papillomavirus E7-induced rereplication and shed light on mechanisms by which human papillomavirus induces genomic instability.
ATR (zeige ANTXR1 Antikörper), activated after DNA damage, phosphorylates Cdt2 (zeige DTL Antikörper) and promotes the rapid degradation of Cdt1 after UV irradiation in the G1 phase of the cell cycle.
A lethal phenotype was seen in four individuals with compound heterozygous CDT1 mutations
conserved arginine residues play critical roles in interaction with Geminin (zeige GMNN Antikörper) and Mcm that are crucial for proper conformation of the complexes and its licensing activity.
Study shows that ablation of Geminin (zeige GMNN Antikörper) induces massive rereplication as a result of unrestrained Cdt1 activity in embryonic stem cells, whereas it has no such effect in embryonic fibroblasts in which alternative regulation of Cdt1 activity is intact.
This study reveals a conserved new regulatory Cdt1 domain crucial for proper DNA licensing activity.
Structure and mutagenesis studies of the C-terminal region of licensing factor Cdt1 enable the identification of key residues for binding to replicative helicase (zeige DNA2 Antikörper) Mcm proteins.
Determined the structures of mCdt1CS (mCdt1C_small; residues 452 to 557) and mCdt1CL (mCdt1C_large; residues 420 to 557) using X-ray crystallography and NMR. This study reveals that Cdt1 is formed with a tandem repeat of the winged helix domain.
Cdt1 function is negatively regulated by the Cdk (zeige CDK4 Antikörper) phosphorylation independent of geminin (zeige GMNN Antikörper) binding
crystal structure of the mouse geminin (zeige GMNN Antikörper)-Cdt1 complex using tGeminin (residues 79-157, truncated geminin (zeige GMNN Antikörper)) and tCdt1 (residues 172-368, truncated Cdt1)
In situ hybridization and immunohistochemistry localize Cdt1 as well as geminin (zeige GMNN Antikörper) to the proliferative compartment of the developing mouse gut (zeige GUSB Antikörper) epithelium
Cdt1 expression characterizes progenitor cells in G1 phase
These results suggested that, at least in vitro, oleic acid-containing cell membranes of the lipid bilayer inhibit Cdt1-geminin (zeige GMNN Antikörper) complex formation by binding to Cdt1 and thereby liberating Cdt1 from inhibition by geminin (zeige GMNN Antikörper).
The results showed that the Cdt1 region spanning amino acids (a. a.) 255-620 is required for efficient inhibition of DNA replication, and that, within this region, a. a. 255-289 have a critical role in inhibition.
These findings suggested that excess Cdt1 suppressed the progression of replication forks.
Dynamic interactions of high Cdt1 and geminin (zeige GMNN Antikörper) levels regulate S phase in early Xenopus embryos.
p97 (zeige vcp Antikörper) is an essential regulator of DNA damage-dependent CDT1 destruction
CDC-48/p97 (zeige vcp Antikörper) coordinates CDT-1 degradation with GINS chromatin dissociation to ensure faithful DNA replication
Loading of geminin (zeige GMNN Antikörper) onto chromatin requires Cdt1, suggesting that geminin (zeige GMNN Antikörper) is targeted at replication origins.
results allow us to build a comprehensive model of how re-replication of DNA is prevented in Xenopus, with Cdt1 regulation being the key feature
Removal of Cdt1 from chromatin and its nuclear exclusion in G2 is critical in regulating licensing and limiting DNA replication in S phase to only one round.
Cdt1 and DDB1 interact in extracts, and DDB1 chromatin loading is dependent on the binding of Cdt1 to PCNA, which indicates that PCNA docking activates the pre-formed Cdt1-Cul4(DDB1) ligase complex.
The protein encoded by this gene is involved in the formation of the pre-replication complex that is necessary for DNA replication. The encoded protein can bind geminin, which prevents replication and may function to prevent this protein from initiating replication at inappropriate origins. Phosphorylation of this protein by cyclin A-dependent kinases results in degradation of the protein.
chromatin licensing and DNA replication factor 1
, DNA replication factor Cdt1-like
, DNA replication factor Cdt1
, Double parked, Drosophila, homolog of
, double parked homolog
, retroviral insertion site 2 protein
, retroviral integration site 1
, retroviral integration site 2
, DNA replication factor