WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the primary antibody was used at 4℃, over night with a 1:5000 dilution . The Dylight 800-conjugated Goat anti-Rabbit antibody was used to detect the antibody. Lane1: PC-12 - Rat adrenal pheochromocytoma Lane2: 3T3-L1 - Mouse embryonic fibroblast Lane3: PC-3 - Human prostate adenocarcinoma Lane4: U-14 - Mouse cervical carcinoma.
WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-Vimentin antibody. The HRP-conjugated Goat anti-Rabbit IgG(H + L) antibody was used to detect the antibody. Lane 1: Hela Lane 2: U2OS Lane 3: C6 Lane 4: U-14.
WB
Western blot analysis of lysates from Hela WT and knockdown cell. Cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with Vimentin Rabbit mAb. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.
IHC
Human colon was stained with anti-Vimentin rabbit antibody.
IHC
Mouse colon was stained with anti-Vimentin rabbit antibody.
IHC
Rat colon was stained with anti-Vimentin rabbit antibody.
ICC/IF
Immunofluorescence analysis of Hela cell. 1,Vimentin Antibody(green) was diluted at 1:200(4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 was diluted at 1:1000(room temperature, 50min). 3 DAPI(blue) 10min.
ICC/IF
Rat skin was stained with anti-Vimentin Rabbit antibody.
ICC/IF
Immunofluorescence analysis of HEK293. Picture A: Vimentin antibody (red). Picture B: DAPI (blue). Picture C: Merge of A+B.