WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the primary antibody was used at 4°C, over night with a 1:2500 dilution . The Dylight 800-conjugated Goat anti-Rabbit antibody was used to detect the antibody. Lane1: HL60 - Human promyelocytic leukemia cell, Lane2: HUVEC - Human umbilical vein endothelial cell, Lane3: Human CAF - Human cancer-associated fibroblast, Lane4: HCT116 - Human colorectal carcinoma, Lane5: A549 - Human lung carcinoma, Lane6: Jurkat - Human T lymphocyte leukemia, Lane7: HT22 - Mouse hippocampal neuronal, Lane8: Thp-1 - Human monocytic leukemia, Lane9: HK-2 - Human proximal tubular epithelial, Lane10: PC-12 - Rat adrenal pheochromocytoma, Lane11: 3T3-L1 - Mouse embryonic fibroblast, Lane12: PC-3 - Human prostate adenocarcinoma, Lane13: U-14 - Mouse cervical carcinoma, Lane14: 293F - HEK293 derivative.
WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-Glucocorticoid Receptor antibody. The HRP-conjugated Goat anti-Rabbit IgG(H + L) antibody was used to detect the antibody. Lane 1: U-251 MG, Lane 2: A549, Lane 3: RAW264.7.
IHC
Rat liver was stained with anti-Glucocorticoid Receptor rabbit antibody.
IHC
Human liver was stained with anti-Glucocorticoid Receptor rabbit antibody.
IHC
Mouse liver was stained with anti-Glucocorticoid Receptor rabbit antibody.
ICC/IF
Immunofluorescence analysis of HEK293. Picture A:Glucocorticoid Receptor antibody (red). Picture B: DAPI (blue). Picture C: Merge of A+B.
IF-P
Rat liver was stained with anti-Glucocorticoid Receptor rabbit antibody