Primary Antibodies
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![Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with ZEB1 antibody [N2C1], Internal (GRP490) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://www.grp-ak.de/media/catalog/product/z/e/zeb1-antibody-n2c1-internal_grp490_wb_2_2.jpg)
![ZEB1 antibody [N2C1], Internal detects ZEB1 protein at nucleus by immunofluorescent analysis.Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: ZEB1 protein stained by ZEB1 antibody [N2C1], Internal (GRP490) diluted at 1:500.Red:](https://www.grp-ak.de/media/catalog/product/z/e/zeb1-antibody-n2c1-internal_grp490_if_1_2.jpg)
![Glyoxalase I antibody [N1C3] detects Glyoxalase I protein at cytoplasm and nucleus by immunofluorescent analysis.Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: Glyoxalase I protein stained by Glyoxalase I antibody [N1C3] (GRP](https://www.grp-ak.de/media/catalog/product/g/l/glyoxalase-i-antibody-n1c3_grp492_if_1_2.jpg)
![Glyoxalase I antibody [N1C3] detects Glyoxalase I protein at cytoplasm by immunohistochemical analysis.Sample: Paraffin-embedded human ovarian cancer.Glyoxalase I stained by Glyoxalase I antibody [N1C3] (GRP492) diluted at 1:500.Antigen Retrieval: Citrate](https://www.grp-ak.de/media/catalog/product/g/l/glyoxalase-i-antibody-n1c3_grp492_ihc-p_1_2.jpg)
![Non-transfected (–) and transfected (+) unboiled 293T whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with GPR30 antibody [C2C3], C-term (GRP493) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody](https://www.grp-ak.de/media/catalog/product/g/p/gpr30-antibody-c2c3-c-term_grp493_wb_1_2.jpg)
