Rabbit anti-β-Tubulin Monoclonal Antibody

WB result of β-Tubulin Rabbit mAb Primary antibody: β-Tubulin Rabbit mAb at 1/1000 dilution Lane 1: Hela whole cell lysate 20 µg Secondary antibody: #abs20040 at 1/10000 dilution Predicted MW: 55 kDa Observed MW: 55 kDa Exposure time: 15 seconds

WB result of β-Tubulin Rabbit mAb Primary antibody: β-Tubulin Rabbit mAb at 1/1000 dilution Lane 1:Mouse brain lysate 20 µg Lane 2: NIH/3T3 whole cell lysate 20 µg Secondary antibody: #abs20040 at 1/10000 dilution Predicted MW: 55 kDa Observed MW: 55 kDa Exposure time: Lane 1: 6 seconds; Lane 2: 15s

IHC shows positive staining in paraffin-embedded human testis. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded human cerebral cortex. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded mouse liver. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

IHC shows positive staining in paraffin-embedded rat kidney. Anti-β-tubulin antibody was used at 1/1000 dilution, Secondary antibody: #abs20040 Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

ICC shows cytoplasm staining in HeLa cells. Anti-β-tubulin antibody was used at 1/250 dilution and incubated overnight at 4°C. Secondary antibody: #abs20025 at 1/1000 dilution.The cells were fixed with 100% Methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were countersained with DAPI.

ICC shows cytoplasm staining in NIH3T3 cells. Anti-β-tubulin antibody was used at 1/250 dilution and incubated overnight at 4°C. Secondary antibody: #abs20025 at 1/1000 dilution.The cells were fixed with 100% Methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were countersained with DAPI.

Flow cytometric analysis of HeLa cells labelling β-tubulin antibody at 1/500 (0.1ug) dilution/ (red) compared with a Rabbit monoclonal IgG (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Secondary antibody：#abs20025.