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Primary antibody against α tubulin

Manufactured by Merck Group

The primary antibody against α-tubulin is a laboratory reagent used for the detection and localization of α-tubulin, a key structural component of microtubules in eukaryotic cells. This antibody can be used in various immunochemical techniques, such as Western blotting, immunofluorescence, and immunohistochemistry, to study the distribution and dynamics of microtubules within cells.

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2 protocols using primary antibody against α tubulin

1

Western Blot Analysis of EDNRA and CDH2

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Lysis buffer containing 50 mmol/L Tris-HCl, 150 mmol/L NaCl, 1% NP 40, 0.1% SDS, and 0.5% deoxycholate and Protease Inhibitor Cocktail (Roche, Indianapolis, IN, USA) was used to prepare all cell protein lysates. Total protein lysates (25–30 μg) were electrophoresed in SDS–polyacrylamide gel and immunoblotted with an anti-EDNRA antibody (1:200; Santa Cruz Biotechnology, Santa Cruz, CA, USA) or an anti-CDH2 antibody (1:1,000; Santa Cruz Biotechnology). A primary antibody against α-tubulin (1:5,000; Sigma) was used as an internal control.
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2

Comprehensive Antibody Sourcing Protocol

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Primary antibody against α-Tubulin was purchased from Sigma-Aldrich (St Louis, MO). The primary antibody against HSPA12B was a generous gift from Dr. Zhihua Han (East Tennessee State University) [9 ]. The remaining primary antibodies and the companies that supplied them were as follows: Bcl-2, Bax, Cox-2 and p-eNOS (Cell Signaling Technology, Beverly, MA); PCAM-1 and Ki-67 (BD Pharmingen, San Jose, CA); eNOS (BD Biosciences, Bedford, MA); and VEGF, Ang-1 and AKAP12 (Abcam, Cambridge, UK). Celecoxib was obtained from Pfizer Pharmaceuticals LLC (Barceloneta, PR). The TUNEL assay kit was from Promega (Madison, WI). The supersignal west pico chemiluminescent substrate was obtained from Pierce (Rockford, IL).
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