MilliporeSigma
Monoclonal Anti-α-Tubulin antibody produced in mouse
T9026
DM1A
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In order to visualize changes in the cytoskeleton of BV2 cells, cells were treated with LPA 1µM for 24 hours and stained for α-tubulin.
Immunofluorescence
BV2 microglia cells
1/100, 40min at 4°C
5% BSA
Cy3, 1/300, 30min at 4°C
N/A
Confocal Microscopy
Treatment with LPA altered the morphology of BV2 microglia cells.
Very clear and reproducible results
None
Very good antibody for visualizing the cytoskeleton of microglia cells.