Transgelin/TAGLN/SM22 alpha Antibody (JE60-72)

Western Blot: Transgelin/TAGLN/SM22 alpha Antibody (JE60-72) [NBP3-32992]

Western Blot: Transgelin/TAGLN/SM22 alpha Antibody (JE60-72) [NBP3-32992] - Western blot analysis of Transgelin/TAGLN/SM22 alpha on Caco-2 cell lysates with Rabbit anti-Transgelin/TAGLN/SM22 alpha antibody (NBP3-32992) at 1/2,000 dilution.

Lysates/proteins at 20 ug/Lane.

Predicted band size: 23 kDa
Observed band size: 23 kDa

Exposure time: 1 minutes 34 seconds;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32992) at 1/2,000 dilution was used in 5% NFDM/TBST at 4C overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.

Immunohistochemistry: Transgelin/TAGLN/SM22 alpha Antibody (JE60-72) [NBP3-32992]

Immunohistochemistry: Transgelin/TAGLN/SM22 alpha Antibody (JE60-72) [NBP3-32992] - Immunohistochemical analysis of paraffin-embedded human endometrium tissue with Rabbit anti-Transgelin/TAGLN/SM22 alpha antibody (NBP3-32992) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32992) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Flow Cytometry: Transgelin/TAGLN/SM22 alpha Antibody (JE60-72) [NBP3-32992]

Flow Cytometry: Transgelin/TAGLN/SM22 alpha Antibody (JE60-72) [NBP3-32992] - Flow cytometric analysis of Caco-2 cells labeling Transgelin/TAGLN/SM22 alpha.

Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32992, 1μg/mL) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).