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BUB1B encodes a kinase involved in spindle checkpoint function. Zusätzlich bieten wir Ihnen BUB1B Antikörper (180) und BUB1B Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.
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Together, our findings demonstrate that Bub1 (zeige BUB1 ELISA Kits) acts at multiple points to assure the correct kinetochore formation.
The Bub3 (zeige BUB3 ELISA Kits)-BubR1 complex on broken DNA inhibits the APC (zeige APC ELISA Kits)/C locally via the sequestration of Cdc20 (zeige CDC20 ELISA Kits).
a model in which Polo (zeige PLK1 ELISA Kits) controls Mps1-dependent BubR1 phosphorylation to promote Cdc20 (zeige CDC20 ELISA Kits) kinetochore recruitment and sustained SAC (zeige ADCY10 ELISA Kits) function.
Data show that the Mad2 (zeige MAD2L1 ELISA Kits) kinetochore dimerization recruitment mechanism is conserved and that the recruitment of Cdc20 (zeige CDC20 ELISA Kits) to kinetochores in Drosophila requires BubR1 but not Mad2 (zeige MAD2L1 ELISA Kits).
Reduced BubR1 or Polo (zeige PLK1 ELISA Kits) function results in abnormal segregation of acentric chromatids, a decrease in acentric chromosome tethering, and a great reduction in adult survival.
BubR1's role in mitosis is discussed.
BubR1 is required for normal synchrony and progression of syncytial nuclei through mitosis and to maintain the mitotic arrest of the polar body chromosomes after completion of meiosis
BubR1 is required to promote stable microtubule kinetochore attachment. Activation of the mechanism that corrects inappropriate kinetochore attachment requires the antagonistic effects of BubR1 and CENP-E (zeige CENPE ELISA Kits).
Recruitment of BubR1 by dysfunctional telomeres inhibits Cdc20 (zeige CDC20 ELISA Kits)-APC (zeige APC ELISA Kits) function, preventing the metaphase-to-anaphase transition.
Results from phylogenomic study identified of a novel conserved cassette of short linear motifs in BubR1 essential for the spindle checkpoint
BubR1 N-terminal domain was necessary, but not sufficient to protect against aneuploidy and cancer. In contrast, BubR1 lacking the internal Cdc20 (zeige CDC20 ELISA Kits)-binding domain provided protection against both, which coincided with improved microtubule-kinetochore attachment error correction and spindle assembly checkpoint activity.
Low BUB1B expression is associated with Chromophobe Renal Cell Carcinomas.
Whether carriers of pathogenic BUB1B mutations, such as the parents of MVA (zeige MYO5A ELISA Kits) syndrome patients, have an increased risk for cancer remains of interest, as studies in mice have suggested that haploinsufficiency of BUB1B may cause an increase in carcinogen-induced tumors
structure of the PP2A B56-BubR1 complex provides important insights into how the B56 subunit directs the recruitment of PP2A to specific targets.
Overexpression of BUB1B is associated with Invasive Breast Cancer.
we showed that BubR1 and Mad2 (zeige MAD2L1 ELISA Kits) are overexpressed in oral squamous cell carcinoma cell lines and linked such overexpression to attenuated spindle assembly checkpoint activity. We also showed BubR1 overexpression to be associated with advanced stage and tumour size.
The integrity of the mitotic checkpoint (zeige BUB3 ELISA Kits) complex depends on the specific recognition between BubR1 and Bub3 (zeige BUB3 ELISA Kits), for which the BubR1 Gle2 (zeige RAE1 ELISA Kits) binding sequence motif is essential.
We show that kinetochore recruitment of BUBR1 and BUB3 (zeige BUB3 ELISA Kits) by BUB1 (zeige BUB1 ELISA Kits) is dispensable for SAC (zeige ADCY10 ELISA Kits) activation
Data suggest that both BubR1 and SNCG may be promising predictive marker rather than prognostic marker in patients with breast cancer.
Age-related decline in BubR1 impairs adult hippocampal neurogenesis.
Consistent with defective myelination, BubR1(H/H) mice exhibited various motor deficits, including impaired motor strength, coordination, and balance, irregular gait patterns and reduced locomotor activity.
EZH2 (zeige EZH2 ELISA Kits) directly interacted with and stabilized BubR1, an effect driving EZH2 (zeige EZH2 ELISA Kits) into the concert of meiosis regulation.
we quantified the frequency of aneuploidy of three autosomes in the cerebral cortex and cerebellum of adult and developing brain of Bub1b(H/H) mice, which have a faulty mitotic checkpoint (zeige BUB3 ELISA Kits), and Ercc1 (zeige ERCC1 ELISA Kits)(-/Delta7) mice, defective in nucleotide excision repair and inter-strand cross-link repair.we found that Bub1b(H/H), but not Ercc1 (zeige ERCC1 ELISA Kits)(-/Delta7) mice, have a significantly higher frequency of aneuploid nuclei relative to wild-t...
Data show that compound mutant spindle assembly checkpoint components BubR1 and Sgo1 (zeige SGOL1 ELISA Kits) embryonic fibroblasts (MEFs) grew at a much slower rate, and a small fraction of cells exhibited morphologies of senescent cells at early passages.
These data reveal that BubR1 plays a multifaceted role in chromosome segregation during the first meiotic division and suggest that age-related decline of BubR1 is a key determinant of the formation of aneuploid oocytes during aging.
BubR1 (-/-) embryos were aneuploid and had an increased level of premature sister chromatid separation.
Low BubR1 expression almost completely inhibited intimal hyperplasia after carotid ligation by suppressing the proliferation of VSMCs, which was caused, in part, by delayed cell cycle progression.
the loss of BubR1 levels with age is due to a decline in NAD(+) and the ability of SIRT2 (zeige SIRT2 ELISA Kits) to maintain lysine-668 of BubR1 in a deacetylated state, which is counteracted by the acetyltransferase CBP (zeige CREBBP ELISA Kits).
BubR1 insufficiency elicits an aging response that is counteracted by p53 (zeige TP53 ELISA Kits) and involves single or multiple p53 (zeige TP53 ELISA Kits) targets, depending on the tissue type.
This gene encodes a kinase involved in spindle checkpoint function. The protein has been localized to the kinetochore and plays a role in the inhibition of the anaphase-promoting complex/cyclosome (APC/C), delaying the onset of anaphase and ensuring proper chromosome segregation. Impaired spindle checkpoint function has been found in many forms of cancer.
BUB1 budding uninhibited by benzimidazoles 1 homolog beta
, budding uninhibited by benzimidazoles 1 beta
, budding uninhibited by benzimidazoles 1 homolog beta
, mitotic checkpoint serine/threonine-protein kinase BUB1 beta
, budding uninhibited by benzimidazoles 1 homolog beta (yeast)
, mitotic checkpoint serine/threonine-protein kinase BUB1 beta-like
, bub related one
, MAD3/BUB1-related protein kinase
, mitotic checkpoint kinase MAD3L
, budding uninhibited by benzimidazoles 1 homolog, beta