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Anti tgfβrii

Manufactured by Cell Signaling Technology
Sourced in United States

Anti-TGFβRII is a primary antibody that recognizes the TGF-beta Receptor II protein. It is designed for use in various research applications, such as Western blotting, immunoprecipitation, and immunohistochemistry, to detect and analyze the expression and localization of TGF-beta Receptor II in biological samples.

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3 protocols using anti tgfβrii

1

Immunoprecipitation and Western Blot Analysis

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Ker-CT cultures were cultured and treated as described. Protein G Dynabeads Immunoprecipitation Kit was used according to manufactures protocol (ThermoFisher). Western blot was performed as described (25 (link)). Anti-caveolin (Cell Signaling, Danvers, MA), anti- TGF-βRII (Cell Signaling), anti-TGF-βRI (Abcam, Cambridge, MA), were used at the recommended dilution and IR labeled secondary antibody(s) (Licor, Lincoln, NE) were used at 1:10000 – 1:20,000. Blots were imaged via the Licor Oddyssey CLx imaging system (Licor).
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2

Western Blot Analysis of Immune Signaling

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Cell lysates were electrophoresed on SDS-PAGE gels (4–15% gradient polyacrylamide gels, BioRad, Hercules, CA, USA) and blots of the gels were probed with the following antibodies: anti-IL-2Rβ Novus, Littleton, CO, USA), anti-TGFβRII, anti-pSTAT5 (Tyr694), anti-STAT5, anti-pSmad3 (Ser423/Ser425), anti-Smad3, and anti-β-actin (all Cell Signaling, Beverly, MA, USA). The secondary Ab used were anti-rabbit IgG IRDye 800CW and anti-mouse IgG IRDye 680LT (LI-COR, Lincoln, NE, USA). Membranes were imaged using the Odyssey Infrared Imager and quantified using Image Studio v2.0 software (LI-COR).
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3

Western Blot Analysis of Immune Signaling

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Cell lysates were electrophoresed on SDS-PAGE gels (4–15% gradient polyacrylamide gels, BioRad, Hercules, CA, USA) and blots of the gels were probed with the following antibodies: anti-IL-2Rβ Novus, Littleton, CO, USA), anti-TGFβRII, anti-pSTAT5 (Tyr694), anti-STAT5, anti-pSmad3 (Ser423/Ser425), anti-Smad3, and anti-β-actin (all Cell Signaling, Beverly, MA, USA). The secondary Ab used were anti-rabbit IgG IRDye 800CW and anti-mouse IgG IRDye 680LT (LI-COR, Lincoln, NE, USA). Membranes were imaged using the Odyssey Infrared Imager and quantified using Image Studio v2.0 software (LI-COR).
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