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Anti alpha tubulin mouse monoclonal antibody

Manufactured by Santa Cruz Biotechnology
Sourced in United States

The Anti-alpha-tubulin mouse monoclonal antibody is a laboratory reagent designed for the detection and study of alpha-tubulin, a key structural component of microtubules in eukaryotic cells. This antibody can be used in various immunoassay techniques to identify and quantify the presence of alpha-tubulin in biological samples.

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2 protocols using anti alpha tubulin mouse monoclonal antibody

1

Antibody Optimization for Western Blotting and Immunofluorescence

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The following antibodies were used: anti-SMN mouse monoclonal antibody (cat. no. 610647, BD Transduction Laboratories; work dilution for Western blotting, 1:10,000; for immunofluorescence, 1:150); anti-ABC1 mouse monoclonal antibody (cat. no. sc-53482 Santa Cruz Biotechnology, Dallas, TX, USA; work dilution for Western blotting, 1:200); anti-alpha-tubulin mouse monoclonal antibody (cat. no. T6074, Sigma-Aldrich, St. Louis, MO, USA; work dilution for Western blotting, 1:2000). The secondary antibodies conjugated to horseradish peroxidase were purchased from Jackson ImmunoResearch Laboratories (West Grove, PA, USA) and used at a dilution of 1:5000. The Alexa Fluor488-conjugated secondary antibodies were purchased from Thermo Fisher (Waltham, MA, USA), and were used at a dilution of 1:200. Filipin (cat. no. F-9765) was purchased from Sigma-Aldrich.
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2

4HNE-Protein Adduct Quantification in Cardiac Samples

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Western blot was performed as described earlier.35 (link),36 (link) In brief, cardiac protein samples were separated on sodium dodecyl sulphate (SDS)-polyacrylamide gels by electrophoresis and the proteins transferred to immobilon-P membranes (Millipore, Billerica, MA). Levels of 4HNE-protein adducts in heart samples were determined using an antibody of 4HNE-Cys/His/Lys (Calbiochem) at a concentration of 1: 1000. Anti-alpha-tubulin mouse monoclonal antibody at a concentration of 1: 1000 (Santa Cruz Biotechnology, Santa Cruz) was used as a housekeeping marker. The bound antibody was visualized with horseradish peroxidase (HRP)-coupled secondary antibody.
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