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 CDC25B Antikörper:
anti-Mouse (Murine) CDC25B Antikörper:
anti-Rat (Rattus) CDC25B Antikörper:
Sie gelangen zu unserer vorgefilterten Suche.
Mouse (Murine) Polyclonal CDC25B Primary Antibody für WB - ABIN871399
Li, Park, Liang, Zhao: Cell cycle G2/M arrest through an S phase-dependent mechanism by HIV-1 viral protein R. in Retrovirology 2010
Show all 4 Pubmed References
Human Polyclonal CDC25B Primary Antibody für IHC (p), WB - ABIN391380
Uchida, Ohtsubo, Shimura, Hirata, Nakagama, Matsunaga, Yoshida, Ishizaka, Yamashita: Nuclear export signal in CDC25B. in Biochemical and biophysical research communications 2004
Show all 2 Pubmed References
miR (zeige MLXIP Antikörper)-152 was a tumor suppressor in EC that inhibited proliferation of human endometrial cancer cells via inducing G2/M phase arrest by suppressing CDC25B expression.
High CDC25B expression is associated with non-small cell lung cancer metastasis.
YWHAE (zeige YWHAE Antikörper) silencing induces cell proliferation, invasion and migration through the up-regulation of CDC25B and MYC (zeige MYC Antikörper) in gastric cancer cells.
our study demonstrate that KCTD12 (zeige KCTD12 Antikörper) binds to CDC25B and activates CDK1 (zeige CDK1 Antikörper) and Aurora A (zeige AURKA Antikörper) to facilitate the G2/M transition and promote tumorigenesis and that Aurora A (zeige AURKA Antikörper) phosphorylates KCTD12 (zeige KCTD12 Antikörper) at serine 243 to trigger a positive feedback loop, thereby potentiating the effects of KCTD12 (zeige KCTD12 Antikörper). Thus, the KCTD12 (zeige KCTD12 Antikörper)-CDC25B-CDK1 (zeige CDK1 Antikörper)-Aurora A (zeige AURKA Antikörper) axis has important implications for cancer diagnoses and prognoses.
While the low expression level of DUSP7 (zeige DUSP7 Antikörper) was restricted to patients with positive rheumatoid factor and anti-citrullinated protein antibodies, the altered expression of CDC25B correlated with the activity of early arthritis.
Conformational flexibility of the complete catalytic domain of Cdc25B phosphatase has been demonstrated.
Data indicate that nine compounds were identified with Ki values for CDC25A, -B and -C ranging from 0.01 to 4.4 muM.
High CDC25B expression is associated with esophageal carcinoma.
Solution NMR studies reveal no global flexibility in the structure of CDC25b catalytic domain
For the first time, we demonstrate that miRNA-211 is a direct negative regulator of CDC25B expression in TNBC cells, alters other related target proteins CCNB1 (zeige CCNB1 Antikörper) and FOXM1 (zeige FOXM1 Antikörper), and then inhibits breast cancer cells growth, migration, and invasion
data suggest an important role of CDC25B for microtubule nucleation and organization. N-terminal of CDC25B is required for regulating the microtubule dynamics and mitotic function.
LSD1 (zeige KDM1A Antikörper) is essential for oocyte meiotic progression by upregulating CDC25B expression.
The role of Cdc25c (zeige CDC25C Antikörper) and Cdc25b in activating G2/M cell cycle checkpoint in zygote.
AURKA (zeige AURKA Antikörper) induced phosphorylation and recruitment of CDC25B to MTOCs prior to p-Cyclin B1 (zeige CCNB1 Antikörper)-Ser123, and this sequential regulation is essential for the commitment of the oocytes to resume meiosis.
Data indicate that 14-3-3epsilon is required for the mitotic entry in the fertilized mouse eggs and responsible for sequestering the CDC25B in cytoplasm. Its binding to CDC25B-S321 phosphorylated by PKA induces mitotic arrest.
Ser321 of Cdc25B is the specific binding site for 14-3-3epsilon binding.
Protein kinase A the early development of mouse embryos by phosphorylation of S149 and S321 of CDC25B, which plays an important role in the regulation of G(2)/M transition in the mitotic cell cycle of fertilized mouse eggs.
In the DNA damage response, instead of inhibiting cyclin B-CDK1 (zeige CDK1 Antikörper) through destruction of Cdc25A (zeige CDC25A Antikörper) phosphatase, oocytes utilize an inhibitory phosphorylation of Cdc25B.
Cdc25B overexpression in early mouse two-cell embryos reverses two-cell block and promotes their development into four-cell stage by activating MPF (zeige MSLN Antikörper).
MCPH1 (zeige MCPH1 Antikörper), through its function in the Chk1 (zeige CHEK1 Antikörper)-Cdc25 (zeige CDC25C Antikörper)-Cdk1 (zeige CDK1 Antikörper) pathway to couple the centrosome cycle with mitosis, is required for precise mitotic spindle orientation and thereby regulates the progenitor division mode to maintain brain size.
CDC25B is a member of the CDC25 family of phosphatases. CDC25B activates the cyclin dependent kinase CDC2 by removing two phosphate groups and it is required for entry into mitosis. CDC25B shuttles between the nucleus and the cytoplasm due to nuclear localization and nuclear export signals. The protein is nuclear in the M and G1 phases of the cell cycle and moves to the cytoplasm during S and G2. CDC25B has oncogenic properties, although its role in tumor formation has not been determined. Multiple transcript variants for this gene exist.
cell division cycle 25 homolog B
, cell division cycle 25 homolog B (S. pombe)
, M-phase inducer phosphatase 2-like
, m-phase inducer phosphatase 2-like
, cell division cycle 25B
, M-phase inducer phosphatase 2
, dual specificity phosphatase Cdc25B