WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the primary antibody was used at 4℃, over night with a 1:10000 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 Lane5: 293F - HEK293 derivative, adapted for suspension culture.
WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-Histone H3 antibody. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody. Lane 1: Hela Lane 2: 3T3-L1 Lane 3: K562 Lane 4: C6 .
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 Histone H3 Rabbit mAb. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.
IHC
Human kidney was stained with anti-Histone H3 rabbit antibody.
IHC
Mouse colon was stained with anti-Histone H3 rabbit antibody.
IHC
Rat colon was stained with anti-Histone H3 rabbit antibody.
ICC/IF
Immunofluorescence analysis of Hela cell. 1,Histone H3 Antibody(red) was diluted at 1:200(4° overnight). LC3A mouse Monoclonal Antibody(5G10)(green) was diluted at 1:200(4° overnight). 2, Goat Anti Rabbit Alexa Fluor 594 was diluted at 1:1000(room temperature, 50min). Goat Anti Mouse Alexa Fluor 488 was diluted at 1:1000(room temperature, 50min).
ICC/IF
Rat liver was stained with anti-Histone H3 Rabbit antibody.
ICC/IF
Immunofluorescence analysis of HeLa. Picture A: Histone H3 Rabbit mAb (red). Picture B: DAPI (blue). Picture C: Merge of A+B.