Mouse Monoclonal MCPyV_gp3 large T antigen antibody. Suitable for WB, ICC/IF and reacts with Merkel cell polyomavirus samples. Cited in 5 publications.
Preservative: 0.02% Sodium azide
Constituents: PBS
WB | ICC/IF | |
---|---|---|
Merkel cell polyomavirus | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Merkel cell polyomavirus | Dilution info 0.25000-0.50000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Merkel cell polyomavirus | Dilution info 5 µg/mL | Notes - |
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Mouse Monoclonal MCPyV_gp3 large T antigen antibody. Suitable for WB, ICC/IF and reacts with Merkel cell polyomavirus samples. Cited in 5 publications.
Preservative: 0.02% Sodium azide
Constituents: PBS
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MCPyV_gp3 large T antigen also known as Merkel cell polyomavirus large T antigen is an important protein involved in the viral replication and transformation processes of Merkel cell polyomavirus (MCPyV). This antigen has an approximate mass of 90 kDa and is primarily expressed in cells infected by MCPyV. The large T antigen is named for its ability to bind to and inactivate tumor suppressor proteins which plays a role in the virus's oncogenic potential.
The large T antigen serves as a multifunctional protein involved in viral replication cell cycle regulation and DNA damage response. Its function as a viral oncoprotein places it in the heart of tumor development processes. Large T antigen forms part of a complex with host cellular proteins assisting in the disruption of normal cellular controls that prevent tumor formation. This disruption is achieved by binding to cellular tumor suppressors such as p53 and retinoblastoma (Rb) proteins.
The large T antigen is involved in cell cycle regulation and tumorigenesis pathways. It plays a substantial role in interfering with the Rb pathway which regulates cell cycle progression. This antigen also impacts the p53 pathway by binding and inactivating the p53 protein preventing apoptosis and contributing to uncontrolled cell proliferation. Both pathways are tightly regulated processes that when dysregulated contribute to oncogenesis.
The large T antigen of MCPyV is closely associated with Merkel cell carcinoma a rare but aggressive skin cancer. This cancer frequently arises from the integration of MCPyV DNA into the host genome and the expression of the large T antigen is a critical factor in these cancerous cells. Contacts with host proteins like p53 and Rb underline the antigen's role in the oncogenic processes leading to cancer development. Additionally research suggests potential associations with other disorders related to immune evasion given its role in manipulating host cellular machinery.
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This blot was produced using a 4-12% Bis-tris under the MOPS buffer system. The gel was run at 200V for 55 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was blocked for an hour using 5% milk before ab202866 and Anti-GAPDH antibody [EPR16891] - Loading Control ab181602 (Rabbit anti-GAPDH loading control) were incubated overnight at 4°C at a 0.5ug/ml concentration and 1/20000 dilution respectively. Antibody binding was detected using Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772) and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777) secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-MCPyV_gp3 large T antigen antibody [ab3] (ab202866) at 0.5 µg/mL
Lane 1: MKL-1 whole cell lysate at 20 µg
Lane 2: HeLa whole cell lysate at 20 µg
Lane 3: HEK293 whole cell lysate at 20 µg
Performed under reducing conditions.
Observed band size: 48 kDa
ab202866 staining MCPyV_gp3 large T antigen in MKL-1 cells. The cells were fixed with 4% PFA (10min), permeabilized with 0.1%PBS-Tween for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1%PBS-Tween for 1h. The cells were then incubated overnight at +4°C with ab202866 at 5μg/ml and Anti-beta Tubulin antibody - Loading Control ab6046, Rabbit polyclonal to beta Tubulin - Loading Control, at 1/1000 dilution. Cells were then incubated with Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed ab150117, Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (shown in green) and Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080, Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor® 594) at 1/1000 dilution (shown in pseudocolor red). Nuclear DNA was labelled with DAPI (shown in blue).
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
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