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anti-Human Aurora Kinase C Antikörper:
anti-Mouse (Murine) Aurora Kinase C Antikörper:
anti-Rat (Rattus) Aurora Kinase C Antikörper:
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Human Polyclonal Aurora Kinase C Primary Antibody für WB - ABIN1882164
Kimura, Matsuda, Yoshioka, Okano: Cell cycle-dependent expression and centrosome localization of a third human aurora/Ipl1-related protein kinase, AIK3. in The Journal of biological chemistry 1999
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Cow (Bovine) Polyclonal Aurora Kinase C Primary Antibody für WB - ABIN2785453
Lee, Lim, Park, Lee, Han, Kim, Cheang, Lee, Lee, Ko, Jang, Kim, Miniaci, Bartsch, Kim, Bailey, Kandel, Kaang: Nuclear translocation of CAM-associated protein activates transcription for long-term facilitation in Aplysia. in Cell 2007
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Human Polyclonal Aurora Kinase C Primary Antibody für WB - ABIN390979
Burum-Auensen, Skotheim, Schjølberg, Røislien, Lothe, Clausen: Spindle proteins are differentially expressed in the various histological subtypes of testicular germ cell tumors. in Journal of carcinogenesis 2010
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Human Polyclonal Aurora Kinase C Primary Antibody für ELISA, WB - ABIN4282476
Dieterich, Zouari, Harbuz, Vialard, Martinez, Bellayou, Prisant, Zoghmar, Guichaoua, Koscinski, Kharouf, Noruzinia, Nadifi, Sefiani, Lornage, Zahi, Viville, Sèle, Jouk, Jacob, Escalier, Nikas et al.: The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population. ... in Human molecular genetics 2009
Human Polyclonal Aurora Kinase C Primary Antibody für WB - ABIN4890463
Doyle, Lee, Selesniemi, Styer, Rueda: The impact of vitrification on murine germinal vesicle oocyte In vitro maturation and aurora kinase A protein expression. in Journal of assisted reproduction and genetics 2014
The epigenetic targets AURKB (zeige AURKB Antikörper), AURKC and DNMT3B (zeige DNMT3B Antikörper), and the global DNA methylation (zeige HELLS Antikörper) profile are regulated during HIV-1 replication in CD4 (zeige CD4 Antikörper)+ T cells, and this regulation can be influenced by the activation state of the cell at the time of infection.
The data suggest that AKA (zeige NEUROG1 Antikörper) is the vertebrate ancestral gene, and that AKB and AKC resulted from gene duplication in placental mammals.
Two novel DMRs, located in RPS6KA4/MIR1237 and the AURKC promoter, were found to be hypermethylated in WT
Identification and characterization of AURKB (zeige AURKB Antikörper) and AURKC variants associated with maternal aneuploidy has been reported.
Aurora-C interactions with members of the Chromosome Passenger Complex (CPC), Survivin and Inner Centromere Protein (INCENP (zeige INCENP Antikörper)) in reference to known Aurora-B (zeige AURKB Antikörper) interactions to understand the functional significance of Aurora-C overexpression in human cancer cells, is reported.
Patients presenting with a monomorphic teratozoospermia such as globozoospermia or macrospermia with more than 85% of the spermatozoa presenting this specific abnormality have been analyzed permitting to identify several key genes for spermatogenesis such as AURKC and DPY19L2 (zeige DPY19L2 Antikörper).
Homozygous c.144delC mutation in AURKC gene in infertile men with macrozoospermia in the Tunisian population
AURKC mutations are more frequent than Klinefelter syndrome and constitute the leading genetic cause of infertility in North African men.
Low AURKC expression is associated with cancer.
Overexpression of AURKC is associated with breast tumors.
findings demonstrate that maternal RNAs regulate AURKC localization and activity in mouse oocytes
The high sequence similarity among the AURK family members has made discerning the individual kinase functions in meiosis challenging. Technical limitations in specifically targeting AURKB (zeige AURKB Antikörper) or AURKC using small-molecule inhibitors and compensatory abilities in single-knockout animals add to this challenge...proper regulation of AURKA (zeige AURKA Antikörper) expression is crucial for spindle formation in meiosis
Three of these mutations AURKC c.144delC (AURKC p.L49Wfs22), AURKC c.686G > A (AURKC p.C229Y) and AURKC c.744C > G (AURKC p.Y248*) are the focus of this study. AURKC p.L49Wfs22 is a loss-of-function mutant that perturbs localization of the chromosomal passenger complex (CPC), AURKC p.C229Y is a hypomorph that cannot fully support cell-cycle progression, and AURKC p.Y248* fails to support chromosome segregation.
These data uncover a role for haspin (zeige GSG2 Antikörper) as a regulator of bipolar spindle assembly by regulating AURKC function at acentriolar microtubule-organizing centers in oocytes.
these data suggest that mammalian oocytes contain AURKC to efficiently execute meiosis I and ensure high-quality eggs necessary for sexual reproduction.
These findings suggest a model for the presence of AURKC in oocytes: that AURKC compensates for loss of AURKB (zeige AURKB Antikörper) through differences in both message recruitment and protein stability.
Overexpressed Aurora-C (aurkc) is an oncogene (zeige RAB1A Antikörper). Overexpression of Aurora-C induces abnormal cell division resulting in centrosome amplification and multinucleation. Cells overexpressing active Aurora-C induced tumour formation.
Conditional deletion of aurora B in somatic cells that do not express aurora C results in chromosomal misalignment and lack of chromosome segregation.
Aurora-C, but not Aurora-B, plays essential roles in female mouse meiosis.
role in regulating the cleavage furrow-specific vimentin (zeige VIM Antikörper) phosphorylation in the cytokinetic process
AURKB (zeige AURKB Antikörper), AURKC, and Thr (zeige TRH Antikörper)-phosphorylated AURKA (zeige AURKA Antikörper) were detected at a contractile ring/midbody during the first polar body extrusion.
This gene encodes a member of the Aurora subfamily of serine/threonine protein kinases. The encoded protein is a chromosomal passenger protein that forms complexes with Aurora-B and inner centromere proteins and may play a role in organizing microtubules in relation to centrosome/spindle function during mitosis. This gene is overexpressed in several cancer cell lines, suggesting an involvement in oncogenic signal transduction. Alternative splicing results in multiple transcript variants.
aurora kinase C
, aurora 3
, aurora-related kinase 3
, aurora/IPL1-related kinase 3
, aurora/IPL1/EG2 protein 2
, serine/threonine kinase 13 (aurora/IPL1-like)
, serine/threonine-protein kinase 13
, serine/threonine-protein kinase aurora-C
, aurora B
, aurora/Ipl1/Eg2 protein 1
, serine/threonine kinase 13 (aurora/IPL-like)