Tested Applications
| Positive WB detected in | Staurosporine treated Ramos cells |
Recommended dilution
| Application | Dilution |
|---|---|
| Western Blot (WB) | WB : 1:500-1:2000 |
| It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
| Sample-dependent, Check data in validation data gallery. | |
Product Information
28953-1-AP targets Phospho-MST1 (Thr183)/MST2 (Thr180) in WB, ELISA applications and shows reactivity with Human samples.
| Tested Reactivity | Human |
| Cited Reactivity | human, mouse, rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen |
Peptide Predict reactive species |
| Full Name | serine/threonine kinase 4 |
| Calculated Molecular Weight | 56 kDa |
| Observed Molecular Weight | 52-56 kDa |
| GenBank Accession Number | BC005231 |
| Gene Symbol | MST1 |
| Gene ID (NCBI) | 6789 |
| RRID | AB_2918221 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Antigen affinity purification |
| UNIPROT ID | Q13043 |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol, pH 7.3. |
| Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA. |
Background Information
Mammalian STE20-like serine-threonine kinase MST1, encoded by the STK4 gene, is a multifunctional protein. MST1 and its closest paralogs MST2 (encoded by the STK3 gene), MST3, and MST4 are members of the Class II Germinal Center Family of Protein Kinases. MST1/2 and LATS1/2 (large tumor suppressor 1 and 2) are core kinase components of the Hippo tumor suppressor pathway in mammalians . In the conventional Hippo pathway, the MST1/2 and LATS1/2 signaling cascade phosphorylates and inactivates the transcriptional coactivator YAP1 (yes associated protein 1) and its close paralog WWTR1]. YAP1 and WWTR1 do not have DNA binding domains and they exert their biological outputs, such as cell proliferation and survival, by interacting with the TEAD1-4 transcription factors. Lines of evidence have indicated that dysregulation or loss of STK4/Hippo signaling is linked to developmental disorders and carcinogenesis with poor prognosis. MST1 is a stress-induced kinase and it can be activated in response to cell-death inducers. Autophosphorylation of MST1 at Thr183 (Thr180 in MST2) in the activation loop is a key activation mechanism for MST1/2 because phosphorylation of Thr183/180 causes the cleavage of MST1 by caspases under apoptotic conditions.
Protocols
| Product Specific Protocols | |
|---|---|
| WB protocol for Phospho-MST1 (Thr183)/MST2 (Thr180) antibody 28953-1-AP | Download protocol |
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols |
Publications
What published studies show
The anti-LATS1 antibody (Cat# 28953-1-AP) has 12 total citations. Citations appear in journals including Cell Death & Disease, International Journal of Biological Sciences, Cell Reports, Chinese Medical Journal, Environmental Pollution, Biochemical Pharmacology, International Journal of Pharmaceutics, Journal of Cellular Physiology, Toxicology and Applied Pharmacology, Discover Oncology, Journal of Natural Medicine, and bioRxiv. Research fields span Hippo pathway signaling, cancer progression (bladder, glioma, lung, renal, pancreatic), apoptosis, cell proliferation, bone development, and muscle atrophy.
| Species | Application | Title |
|---|---|---|
Cell Death Dis PLAGL2 promotes bladder cancer progression via RACGAP1/RhoA GTPase/YAP1 signaling | ||
Int J Biol Sci S100 Calcium Binding Protein A16 Promotes Cell Proliferation by triggering LATS1 ubiquitin degradation mediated by CUL4A ligase to inhibit Hippo pathway in Glioma development | ||
Chin Med J (Engl) GADD45B promotes apoptosis in intestinal ischemia/reperfusion through DNA demethylation of MST1/Hippo. | ||
Cell Rep The STRIPAK complex is required for radial sorting and laminin receptor expression in Schwann cells | ||
Environ Pollut Microcystin-LR facilitates pubertal bone retardation by interfering with glutamine metabolism to accelerate stem cell senescence through Hippo/GLS pathway | ||

