Complement Component C9 Antibody (JE01-45)

Western Blot: Complement Component C9 Antibody (JE01-45) [NBP3-32098]

Western Blot: Complement Component C9 Antibody (JE01-45) [NBP3-32098] - Western blot analysis of Complement Component C9 on different lysates with Rabbit anti-Complement Component C9 antibody (NBP3-32098) at 1/2,000 dilution.

Lane 1: Human plasma tissue lysate
Lane 2: Human serum tissue lysate

Lysates/proteins at 20 ug/Lane.

Predicted band size: 63 kDa
Observed band size: 70 kDa

Exposure time: 10 seconds ECL;

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 (NBP3-32098) 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: Complement Component C9 Antibody (JE01-45) [NBP3-32098]

Immunohistochemistry: Complement Component C9 Antibody (JE01-45) [NBP3-32098] - Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-Complement Component C9 antibody (NBP3-32098) at 1/1,000 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 (NBP3-32098) at 1/1,000 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.

Immunohistochemistry: Complement Component C9 Antibody (JE01-45) [NBP3-32098]

Immunohistochemistry: Complement Component C9 Antibody (JE01-45) [NBP3-32098] - Immunofluorescence analysis of paraffin-embedded human spleen tissue labeling Complement Component C9 with Rabbit anti-Complement Component C9 antibody (NBP3-32098) 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32098, green) at 1/200 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).