
Phospho-Aurora Kinase (Thr288) Rabbit Polyclonal Antibody#abs130639
Please note that the price provided is only for your reference. For detailed pricing information, kindly reach out to our sales representative, Vecent. We recommend contacting Vecent for accurate pricing details. Data Examples Western blot analysis of Aurora Kinase phosphorylation expression in...
Description
Catalog-specification | Delivery time | USD price |
abs130639-50ug | 1-2 Weeks | 201 |
abs130639-100ug | 1-2 Weeks | 301 |
Please note that the price provided is only for your reference. For detailed pricing information, kindly reach out to our sales representative, Vecent. We recommend contacting Vecent for accurate pricing details.
Overview | |
Description | This gene encodes a kinase that is regulated by the cell cycle and is believed to play a crucial role in the formation and stabilization of microtubules at the spindle pole during the segregation of chromosomes. In interphase cells, the protein is located at the centrosome, while in mitosis, it localizes to the spindle poles. Notably, this gene's involvement in tumor development and progression suggests its potential significance in cancer research. |
Other names | Aurora kinase A, also known as AURKA or STK15, is a serine/threonine kinase that plays a crucial role in several cellular processes, including mitosis and cytokinesis. This kinase is encoded by the AURKA gene and is primarily expressed in proliferating cells. Additionally, AURKA has been found to be overexpressed in many types of cancer, including breast, ovarian, and pancreatic cancer. |
Source | Rabbit |
Specificity | The Phospho-Aurora Kinase (Thr288) Antibody is capable of identifying Aurora Kinase only in its phosphorylated state at Threonine 288. This antibody is highly specific and is able to detect endogenous levels of the target protein. Therefore, the Phospho-Aurora Kinase (Thr288) Antibody is an effective tool for studying the role and regulation of Aurora Kinase in various cellular processes. |
| Reactivity | Human;Mouse;Rat |
Predictive reaction species | Xenopus;Rabbit;Pig;Dog;Sheep;Bovine;Horse |
| Antigen | Aurora Kinase |
Application | The recommended dilution range for this antibody is WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-1:500, and ELISA(peptide) 1:20000-1:40000. You can use this information to optimize your experimental design and ensure that you obtain accurate and consistent results. This antibody is highly versatile and can be used for a variety of applications, so be sure to follow the guidelines provided to achieve the best possible outcomes. Whether you are performing Western blotting, immunohistochemistry, immunofluorescence, or ELISA, this antibody is a valuable tool that can help you achieve your research goals. |
| Immunogen | Threonine 288 is the phosphorylation site within human Aurora Kinase. We have successfully synthesized a peptide that is based on the surrounding region of this critical site. This peptide is derived from human Aurora Kinase and has been carefully designed to be highly similar to the original sequence. Its unique structure ensures its affinity and specificity towards the phosphorylated target. Our research team has worked diligently to create this synthesized peptide, which holds great potential for further studies and applications. |
Properties | |
| MW | 48kDa |
| Concentration | 1mg/ml |
Purification | Through sequential chromatography on phospho- and non-phospho-peptide affinity columns, the antibody has been obtained by purifying rabbit serum, resulting in a highly purified form. |
Clonality | Polyclonal Antibody |
| Stability & Storage | Ensure that the product is stored at -20 °C for a period of one year, while also taking care to avoid subjecting it to multiple freeze/thaw cycles. |
Storage buffer | Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.Store at -20 °C.Stable for 12 months from date of receipt. |
Target | |
Background | Mitotic serine/threonine kinase that contributes to the regulation of cell cycle progression. Associates with the centrosome and the spindle microtubules during mitosis and plays a critical role in various mitotic events including the establishment of mitotic spindle, centrosome duplication, centrosome separation as well as maturation, chromosomal alignment, spindle assembly checkpoint, and cytokinesis. Required for initial activation of CDK1 at centrosomes. Phosphorylates numerous target proteins, including ARHGEF2, BORA, BRCA1, CDC25B, DLGP5, HDAC6, KIF2A, LATS2, NDEL1, PARD3, PPP1R2, PLK1, RASSF1, TACC3, p53/TP53 and TPX2. Regulates KIF2A tubulin depolymerase activity. Required for normal axon formation. Plays a role in microtubule remodeling during neurite extension. Important for microtubule formation and/or stabilization. Also acts as a key regulatory component of the p53/TP53 pathway, and particularly the checkpoint-response pathways critical for oncogenic transformation of cells, by phosphorylating and stabilizing p53/TP53. Phosphorylates its own inhibitors, the protein phosphatase type 1 (PP1) isoforms, to inhibit their activity. Necessary for proper cilia disassembly prior to mitosis. |
Tissue specificity | Highly expressed in testis and weakly in skeletal muscle, thymus and spleen. Also highly expressed in colon, ovarian, prostate, neuroblastoma, breast and cervical cancer cell lines. |
| Posttranslational modification | Activated by phosphorylation at Thr-288; this brings about a change in the conformation of the activation segment. Phosphorylation at Thr-288 varies during the cell cycle and is highest during M phase. Autophosphorylated at Thr-288 upon TPX2 binding. Thr-288 can be phosphorylated by several kinases, including PAK and PKA. Protein phosphatase type 1 (PP1) binds AURKA and inhibits its activity by dephosphorylating Thr-288 during mitosis. Phosphorylation at Ser-342 decreases the kinase activity. PPP2CA controls degradation by dephosphorylating Ser-51 at the end of mitosis.Ubiquitinated by the E3 ubiquitin-protein ligase complex SCF(FBXL7) during mitosis, leading to its degradation by the proteasome. Ubiquitinated by CHFR, leading to its degradation by the proteasome (By similarity). Ubiquitinated by the anaphase-promoting complex (APC), leading to its degradation by the proteasome. |
Celluar localization | Cytoskeleton;Cytosol;Nucleus; |
| UniPort | O14965 |
Data Examples

Western blot analysis of Aurora Kinase phosphorylation expression in serum treated 293 whole cell lysates,The lane on the left is treated with the antigen-specific peptide.
This product is for research use only, not for use in diagnostic prodecures or in human.
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