Application
WB analysis of mouse testis lysate (25 ug) using PER1 antibody at a dilution of 1:500.
Application
ICC/IF analysis of HeLa cells was performed in the presence (right) or absence (left) of PER1 antibody at a dilution of 1:100 (green). F-actin (red) was stained with a flourescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.
Application
ICC/IF analysis of SH-SY5Y cells was performed in the presence (right) or absence (left) of PER1 antibody at a dilution of 1:100 (green). F-actin (red) was stained with a flourescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.
Application
ICC/IF analysis of NIH-3T3 cells was performed in the presence (right) or absence (left) of PER1 antibody at a dilution of 1:100 (green). F-actin (red) was stained with a flourescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.
Application
IHC-P analysis of human liver tissue was performed in the presence (right) or absence (left) of PER1 antibody at a dilution of 1:100.
Application
IHC-P analysis of human skeletal muscle was performed in the presence (right) or absence (left) of PER1 antibody at a dilution of 1:100.
Application
IHC-P analysis of mouse skeletal muscle was performed in the presence (right) or absence (left) of PER1 antibody at a dilution of 1:100.