Rabbit Recombinant Monoclonal Serine/threonine-protein kinase 4/MST-1 phospho T180 + T183 antibody. Carrier free. Suitable for WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ICC/IF | IP | Flow Cyt | WB | IHC-P | |
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Human | Not recommended | Not recommended | Not recommended | Tested | Not recommended |
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Stress-activated, pro-apoptotic kinase which, following caspase-cleavage, enters the nucleus and induces chromatin condensation followed by internucleosomal DNA fragmentation. Key component of the Hippo signaling pathway which plays a pivotal role in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. The core of this pathway is composed of a kinase cascade wherein STK3/MST2 and STK4/MST1, in complex with its regulatory protein SAV1, phosphorylates and activates LATS1/2 in complex with its regulatory protein MOB1, which in turn phosphorylates and inactivates YAP1 oncoprotein and WWTR1/TAZ. Phosphorylation of YAP1 by LATS2 inhibits its translocation into the nucleus to regulate cellular genes important for cell proliferation, cell death, and cell migration. STK3/MST2 and STK4/MST1 are required to repress proliferation of mature hepatocytes, to prevent activation of facultative adult liver stem cells (oval cells), and to inhibit tumor formation (By similarity). Phosphorylates 'Ser-14' of histone H2B (H2BS14ph) during apoptosis. Phosphorylates FOXO3 upon oxidative stress, which results in its nuclear translocation and cell death initiation. Phosphorylates MOBKL1A, MOBKL1B and RASSF2. Phosphorylates TNNI3 (cardiac Tn-I) and alters its binding affinity to TNNC1 (cardiac Tn-C) and TNNT2 (cardiac Tn-T). Phosphorylates FOXO1 on 'Ser-212' and regulates its activation and stimulates transcription of PMAIP1 in a FOXO1-dependent manner. Phosphorylates SIRT1 and inhibits SIRT1-mediated p53/TP53 deacetylation, thereby promoting p53/TP53 dependent transcription and apoptosis upon DNA damage. Acts as an inhibitor of PKB/AKT1. Phosphorylates AR on 'Ser-650' and suppresses its activity by intersecting with PKB/AKT1 signaling and antagonizing formation of AR-chromatin complexes.
KRS2, MST1, STK4, Serine/threonine-protein kinase 4, Mammalian STE20-like protein kinase 1, STE20-like kinase MST1, Serine/threonine-protein kinase Krs-2, MST-1
Rabbit Recombinant Monoclonal Serine/threonine-protein kinase 4/MST-1 phospho T180 + T183 antibody. Carrier free. Suitable for WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ab247466 is the carrier-free version of Anti-MST1/MST2 (phospho T180 + T183) antibody [EPR1467Y] ab76323.
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
The MST1/MST2 proteins also known as STK4 and STK3 play mechanical roles as serine/threonine kinases. Each protein has a molecular mass of around 56-58 kDa. They are expressed in many tissues with high levels noted in the liver pancreas and kidney. These proteins exist mainly in the cytoplasm and can translocate to the nucleus upon activation. Activation usually takes place through autophosphorylation at certain residues which further facilitates phosphorylation of downstream substrates.
MST1/MST2 function as core components of the Hippo signaling pathway. They act in a kinase complex together with other proteins like SAV1 LATS1 and MOB1. Their activities involve regulating cell proliferation apoptosis and organ size control. By phosphorylating other signaling molecules they decide whether cells enter apoptosis or continue proliferating impacting cellular homeostasis. MST1/MST2 phosphorylation triggers a cascade that ultimately influences transcriptional control in the nucleus.
Both MST1 and MST2 integrate into the Hippo and Ras signaling pathways. Within the Hippo pathway they phosphorylate large tumor suppressors such as LATS1 and LATS2 which then regulate the transcriptional co-activators YAP and TAZ. This interaction helps determine gene expression associated with cell growth and survival. Hippo pathway's role links with Ras signaling where unchecked activity can lead to oncogenesis. MST1/MST2 function connects with MAP kinase proteins that play parts in oncogenic and apoptotic balance.
MST1 and MST2 exhibit connections to cancer and neurodegenerative diseases. Their regulatory dysfunction can contribute to tumor development due to disrupted cellular homeostasis. Low expression or mutation in MST genes relates to multiple types of cancers including hepatocellular carcinoma. MST1 has an association with neurodegenerative conditions like Alzheimer's disease where its role involves apoptosis-related protein interactions including those with caspases. Proper MST1/MST2 function is essential for maintaining controlled cell growth and apoptosis to prevent such diseases.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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This data was developed using Anti-MST1/MST2 (phospho T180 + T183) antibody [EPR1467Y] ab76323, the same antibody clone in a different buffer formulation.
All lanes: Western blot - Anti-MST1/MST2 (phospho T180 + T183) antibody [EPR1467Y] (Anti-MST1/MST2 (phospho T180 + T183) antibody [EPR1467Y] ab76323) at 1/2000 dilution
Lane 1: HeLa cell lysate, untreated at 10 µg
Lane 2: HeLa cell lysate treated with Calyculin A. at 10 µg
All lanes: Goat anti-rabbit HRP at 1/1000 dilution
Predicted band size: 56 kDa
Observed band size: 59 kDa
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