Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all species
Show all synonyms
Select your species and application
anti-Rat (Rattus) WEE1 Antibodies:
anti-Mouse (Murine) WEE1 Antibodies:
anti-Human WEE1 Antibodies:
Go to our pre-filtered search.
Human Polyclonal WEE1 Primary Antibody for DB, IHC (p) - ABIN389681
Müller, Lutter, Püschel: Persistence of the cell-cycle checkpoint kinase Wee1 in SadA- and SadB-deficient neurons disrupts neuronal polarity. in Journal of cell science 2010
Human Monoclonal WEE1 Primary Antibody for ELISA, WB - ABIN521378
Yue, Zhen, Huang, Zheng, Feng, Jiang, Yang, Wu, Liu, Guo: Proteasome Inhibition Contributed to the Cytotoxicity of Arenobufagin after Its Binding with Na, K-ATPase in Human Cervical Carcinoma HeLa Cells. in PLoS ONE 2016
Human Polyclonal WEE1 Primary Antibody for IP, IHC - ABIN222939
Caffarel, Sarrió, Palacios, Guzmán, Sánchez: Delta9-tetrahydrocannabinol inhibits cell cycle progression in human breast cancer cells through Cdc2 regulation. in Cancer research 2006
Morphine significantly downregulated the expression of miRNA-219-5p, which targets WEE1 to suppress Tyr15 expressions and activate Cdc2 (show CDK1 Antibodies), thus inhibiting the morphine-induced macrophage apoptosis.
Results revealed that WEE1 is indispensable for maintaining genomic stability and it functions as a haploinsufficient tumor suppressor.
Wee1 is directly or indirectly involved in the mechanism of the circadian rhythm-dependent changes in docetaxel-induced intestinal damage.
The induction of Wee1 under hypoxia was confirmed both at the mRNA and protein levels.
In this study, we found that the chromosomal wee1 gene is also down-regulated by KLF3 (show KLF3 Antibodies).
The regulation of Wee1 by SadA (show BRSK2 Antibodies) and SadB (show BRSK1 Antibodies) kinases is essential for the differentiation of polarized neurons.
Mammalian Wee1 plays a critical role in maintaining genome integrity and is essential for embryonic survival at the pre-implantation stage of mouse development.
expression of wee1 was directly regulated by the molecular components of the circadian clockwork in the regenerating liver
transcription repressive activity of TBP-related factor 2 (show TBPL1 Antibodies) to wee1 promoter needs association with the promoter and TFIIA (show GTF2A1 Antibodies)
the suppression of nuclear import of cyclin B1 (show CCNB1 Antibodies), the induction of Wee1 kinase activity, and the transient nuclear accumulation of p21(CIP1/WAF1 (show CDKN1A Antibodies)) may play important roles in the transient cell cycle delay in response to ionizing radiation
miR (show MLXIP Antibodies)-503 could function as an enhancer of radiation responses in laryngeal carcinoma cells by inhibiting WEE1
Data suggest that SMURF1 (show SMURF1 Antibodies) is required for S phase progression; SMURF1 (show SMURF1 Antibodies) promotes ubiquitination-dependent degradation of WEE1; these functions of SMURF1 (show SMURF1 Antibodies) appear to be linked and may be important in cell proliferation and tumorigenesis. (SMURF1 (show SMURF1 Antibodies) = SMAD specific E3 ubiquitin protein ligase 1 (show SMURF1 Antibodies); WEE1 = wee 1 homolog [S pombe] protein)
Date show that when Wee1 alone is inhibited, Chk1 (show CHEK1 Antibodies) suppresses CDC45 (show CDC45 Antibodies) loading and thereby limits the extent of unscheduled replication initiation and subsequent S-phase DNA damage, despite very high CDK (show CDK4 Antibodies)-activity.
we overexpressed CKS1B (show CKS1B Antibodies) in multiple cell lines and found increased sensitivity to PLK1 (show PLK1 Antibodies) knockdown and PLK1 (show PLK1 Antibodies) drug inhibition. Finally, combined inhibition of WEE1 and PLK1 (show PLK1 Antibodies) results in less apoptosis than predicted based on an additive model of the individual inhibitors, showing an epistatic interaction and confirming a prediction of the yeast data.
Wee1 staining intensity was a predictor of favorable metastasis-free and overall survival compared to strong intensity and no or weak staining
These results highlight the key role of WEE1 suppression to combat glioblastomas. Moreover, it showed beneficial possibilities of WEE1 suppression with different anticancer approaches for neurological malignancies.
Wee1 inhibition potentiates Wip1-dependent tumor sensitization effect by reducing levels of Hipk2 kinase, a negative regulator of Wip1 pathway.
High nuclear expression of WEE1 protein is associated with all glioma grades and types.
Consistent with these findings, a genome-scale pooled RNA interference screen revealed that toxic doses of MK-1775 are suppressed by CDK2 (show CDK2 Antibodies) or Cyclin A2 (show CCNA2 Antibodies) knockdown. These findings support G2 exit as the more significant effect of Wee1 inhibition in pancreatic cancers.
WEE1 is regulated at the translational level by CPEB1 (show CPEB1 Antibodies) and miR (show MLXIP Antibodies)-15b in a coordinated and cell-cycle-dependent manner.
the identification of a second member of the RNase H2 complex, RNase H2B (show RNASEH2B Antibodies), being able to complement the root growth phenotype of WEE1(KO) plants, is reported.
mutant alleles of the genes encoding subunits of the ribonuclease H2 (RNase H2) complex, known for its role in removing ribonucleotides from DNA-RNA duplexes, were identified as suppressor mutants of WEE1 knockout plants.
The plant WEE1 kinase acquired an indirect developmental function that is important for meristem maintenance upon replication stress.
The WEE1 gene is not rate-limiting for cell cycle progression under normal growth conditions but is a critical target of the ATR (show ATR Antibodies)-ATM (show ATM Antibodies) signaling cascades that inhibit the cell cycle upon activation of the DNA integrity checkpoints.
This gene encodes a nuclear protein, which is a tyrosine kinase belonging to the Ser/Thr family of protein kinases. This protein catalyzes the inhibitory tyrosine phosphorylation of CDC2/cyclin B kinase, and appears to coordinate the transition between DNA replication and mitosis by protecting the nucleus from cytoplasmically activated CDC2 kinase.
WEE1 homolog (S. pombe)
, wee1-like protein kinase 2
, Wee1 kinase
, Wee1-like protein kinase
, wee1 tyrosine kinase
, wee1-like protein kinase
, wee1A kinase
, WEE1 tyrosine kinase
, WEE1+ homolog