uPAR antibody

Wild-type (WT) and uPAR knockout (KO) HeLa cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with uPAR antibody (GTX100467) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Whole cell extract (30 μg) was separated by 12% SDS-PAGE, and the membranes were blotted with uPAR antibody (GTX100467) diluted at 1:500 and competitor's antibody (CST#12713) diluted at 1:200. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Whole cell extract (30 μg) was separated by 12% SDS-PAGE, and the membrane was blotted with uPAR antibody (GTX100467) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Untreated (–) and treated (+) U937 whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with uPAR antibody (GTX100467) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

uPAR antibody detects uPAR protein at cell membrane by immunohistochemical analysis.
Sample: Paraffin-embedded human lung cancer.
uPAR stained by uPAR antibody (GTX100467) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

uPAR antibody detects uPAR protein at cytoplasm by immunofluorescent analysis.
Sample: A431 cells were fixed in 4% paraformaldehyde at RT for 15 min.
Green: uPAR protein stained by uPAR antibody (GTX100467) diluted at 1:500.
Blue: Hoechst 33342 staining.

uPAR antibody detects uPAR protein at cell membrane by immunohistochemical analysis.
Sample: Paraffin-embedded human lung cancer.
uPAR stained by uPAR antibody (GTX100467) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min