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Anti βiii tubulin tuj1 antibody

Manufactured by Merck Group

The Anti-βIII-tubulin (Tuj1) antibody is a laboratory reagent used for the detection and analysis of the βIII-tubulin protein. βIII-tubulin is a component of the microtubule cytoskeleton and is commonly used as a neuronal marker. The antibody can be used in various immunoassay techniques, such as immunocytochemistry and Western blotting, to identify and quantify the presence of βIII-tubulin in biological samples.

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3 protocols using anti βiii tubulin tuj1 antibody

1

Neuromuscular Junction Visualization in Mouse Diaphragm

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E18.5 mouse embryos were fixed by immersion in 4% (w/v) paraformaldehyde for 24 hours at 4°C. Diaphragms were dissected and washed in phosphate-buffered saline (PBS) before incubation with 10 μg/ml tetramethylrhodamine (TRITC)-conjugated α-bungarotoxin (Thermo Fisher Scientific) for 20 mins at room temperature. Samples were then permeabilized/blocked in PTX (PBS, 0.5% Triton-X100) with 4% BSA (Sigma) for 2 hours at room temperature and incubated overnight at 4 °C with an anti-βIII-tubulin (Tuj1) antibody (Sigma, T2200) in blocking solution (1:500 dilution). Following multiple washes in PTX, diaphragms were incubated with an AlexaFluor488-conjugated anti-rabbit antibody (Thermo Fisher Scientific A11008) (1:200 dilution) in blocking solution for 5 hours at room temperature and again extensively washed in PTX. Diaphragms were finally mounted in Vectashield (Vector Laboratories) and images were acquired on a DMi8 upright fluorescence microscope (Leica Microsystems) coupled to a monochrome digital camera (Hammamatsu C4742-95), using a NPLAN 5X/0.12 objective.
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2

Neuromuscular Junction Visualization in Mouse Diaphragm

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E18.5 mouse embryos were fixed by immersion in 4% (w/v) paraformaldehyde for 24 hours at 4°C. Diaphragms were dissected and washed in phosphate-buffered saline (PBS) before incubation with 10 μg/ml tetramethylrhodamine (TRITC)-conjugated α-bungarotoxin (Thermo Fisher Scientific) for 20 mins at room temperature. Samples were then permeabilized/blocked in PTX (PBS, 0.5% Triton-X100) with 4% BSA (Sigma) for 2 hours at room temperature and incubated overnight at 4 °C with an anti-βIII-tubulin (Tuj1) antibody (Sigma, T2200) in blocking solution (1:500 dilution). Following multiple washes in PTX, diaphragms were incubated with an AlexaFluor488-conjugated anti-rabbit antibody (Thermo Fisher Scientific A11008) (1:200 dilution) in blocking solution for 5 hours at room temperature and again extensively washed in PTX. Diaphragms were finally mounted in Vectashield (Vector Laboratories) and images were acquired on a DMi8 upright fluorescence microscope (Leica Microsystems) coupled to a monochrome digital camera (Hammamatsu C4742-95), using a NPLAN 5X/0.12 objective.
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3

Investigating CaMKII Regulation in Neurons

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KN93 and Blebbistatin were obtained from Selleck Chemicals. CdCl 2 was from Sigma-Aldrich. The anti-βIII tubulin (TUJ1) antibody was from Sigma-Aldrich. Primary antibody against β-actin and phospho-CaMKII were from Cell Signaling Technology. Alexa fluor ® plus 488 or 568 secondary antibodies were purchased from Life Technologies. Dextran biotin (BDA) was purchased from Life Technologies. Cy3-Streptavidin was from Jackson Laboratories.
Actin-stain 555 Fluorescent Phalloidin was from Cytoskeleton. The siRNA against CaMKIIγ was from GenePharma (Shanghai, China) which targeted the following sequences: AACGTGGTACATAATGCTACA, CACAGTCACTCCTGAAGCTAA and ATCATTAAGATCACAGAACAA.
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