Anti-STK3/MST-2 antibody [3067C3a]
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(2 Publications)
Mouse Monoclonal STK3/MST-2 antibody. Suitable for WB and reacts with Recombinant fragment - Human, Human samples. Cited in 2 publications. Immunogen corresponding to Recombinant Fragment Protein within Human STK3.
View Alternative Names
KRS1, MST2, STK3, Serine/threonine-protein kinase 3, Mammalian STE20-like protein kinase 2, STE20-like kinase MST2, Serine/threonine-protein kinase Krs-1, MST-2
- WB
Lab
Western blot - Anti-STK3/MST-2 antibody [3067C3a] (AB71960)
Lane 1 : Wild-type HAP1 cell lysate (20 μg)
Lane 2 : STK3/MST-2 knockout HAP1 cell lysate (20 μg)
Lane 3 : NIH/3T3 cell lysate (20 μg)
Lane 4 : 293T cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab71960 observed at 56 kDa. Red - loading control, ab181602, observed at 37 kDa.
ab71960 was shown to recognize STK3/MST-2 when STK3/MST-2 knockout samples were used, along with additional cross-reactive bands. Wild-type and STK3/MST-2 knockout samples were subjected to SDS-PAGE. ab71960 and ab181602 (loading control to STK3/MST-2) were diluted 1 μg/mL and 1/10 000 respectively and incubated overnight at 4°C. Blots were developed with Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772 and Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777 secondary antibodies at 1/10 000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-STK3/MST-2 antibody [3067C3a] (ab71960)
Predicted band size: 56 kDa
false
- WB
Unknown
Western blot - Anti-STK3/MST-2 antibody [3067C3a] (AB71960)
The molecular weight of the band on the western blot does not correspond to the molecular weight of the natural protein because only a fragment of the protein was used.
All lanes:
Western blot - Anti-STK3/MST-2 antibody [3067C3a] (ab71960)
All lanes:
immunising recombinant protein
Predicted band size: 56 kDa
Observed band size: 37 kDa
false
- WB
Lab
Western blot - Anti-STK3/MST-2 antibody [3067C3a] (AB71960)
Lanes 1- 2 : Merged signal (red and green). Green - ab71960 observed at 56 kDa. Red - Anti-GAPDH antibody[EPR16891] - Loading Control (ab181602) observed at 37 kDa.
ab71960 was shown to react with STK3/MST-2 in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line ab265082 (knockout cell lysate ab257714) was used. Wild-type HeLa and STK3 knockout HeLa cell lysates were subjected to SDS-PAGE. ab71960 and Anti-GAPDH antibody[EPR16891] - Loading Control (ab181602) were incubated overnight at 4°C at a 1 in 10000 Dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye®800CW) preadsorbed (ab216772) and Goat Anti-Rabbit IgG H&L (IRDye®680RD) preadsorbed (ab216777) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-STK3/MST-2 antibody [3067C3a] (ab71960) at 1/10000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
STK3 knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human STK3 (MST-2) knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-stk3-mst-2-knockout-hela-cell-line-ab265082'>ab265082</a>)
Predicted band size: 56 kDa
Observed band size: 56 kDa
false
Reactivity data
Properties and storage information
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
STK3/MST-2 is a core component of the Hippo signaling pathway which controls organ size by regulating cell proliferation and apoptosis. MST-2 often interacts with other proteins and participates in functional complexes notably with MOB1 and LATS1/2. These interactions are essential for transmitting growth inhibitory signals. Through its kinase activity MST-2 phosphorylates and activates these molecules initiating a cascade that ultimately influences gene expression impacting cell cycle and cell death processes.
Pathways
MST-2 plays a pivotal role not only in the Hippo pathway but also in the MAPK signaling network. In the Hippo pathway MST-2 phosphorylates components like LATS1/2 subsequently affecting the translocation and activity of YAP/TAZ transcription factors which control cell proliferation and survival. In the MAPK pathway MST-2 can interact with other kinases such as ASK1 to influence stress response signaling. These interactions demonstrate how MST-2 integrates signals between pathways to mediate critical decisions in cell life and death.
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Target data
Publications (2)
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Cell reports 30:1208-1222.e9 PubMed31995759
2020
Applications
Unspecified application
Species
Unspecified reactive species
The EMBO journal 38:e101168 PubMed31414556
2019
Applications
Unspecified application
Species
Unspecified reactive species
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